Commonly known as parasitic worms, this group includes the ACANTHOCEPHALA; NEMATODA; and PLATYHELMINTHS. Some authors consider certain species of LEECHES that can become temporarily parasitic as helminths.
Infestation with parasitic worms of the helminth class.
Substances that are recognized by the immune system and induce an immune reaction.
Infestation of animals with parasitic worms of the helminth class. The infestation may be experimental or veterinary.
The treatment of immune system diseases by deliberate infestation with helminths. This therapy is partly based on the HYGIENE HYPOTHESIS which states that the absence of parasites increases immune dysregulation because of the lack of stimulation of REGULATORY T-CELLS.
Substances elaborated by bacteria that have antigenic activity.
Any part or derivative of a helminth that elicits an immune reaction. The most commonly seen helminth antigens are those of the schistosomes.
Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS.
Proteins, glycoprotein, or lipoprotein moieties on surfaces of tumor cells that are usually identified by monoclonal antibodies. Many of these are of either embryonic or viral origin.
Antigens on surfaces of cells, including infectious or foreign cells or viruses. They are usually protein-containing groups on cell membranes or walls and may be isolated.
Immunoglobulins produced in a response to HELMINTH ANTIGENS.
Substances elaborated by viruses that have antigenic activity.
A genus of nematode worms comprising the whipworms.
A superfamily of nematode parasitic hookworms consisting of four genera: ANCYLOSTOMA; NECATOR; Bunostomum; and Uncinaria. ANCYLOSTOMA and NECATOR occur in humans and other mammals. Bunostomum is common in ruminants and Uncinaria in wolves, foxes, and dogs.
Agents destructive to parasitic worms. They are used therapeutically in the treatment of HELMINTHIASIS in man and animal.
Proteins found in any species of helminth.
Any part or derivative of any protozoan that elicits immunity; malaria (Plasmodium) and trypanosome antigens are presently the most frequently encountered.
A species of intestinal nematode parasites which occur most commonly in mice. Infection is by ingesting larvae. This particular species is used extensively in immunological research.
Infections with nematodes of the order STRONGYLIDA.
Polyomavirus antigens which cause infection and cellular transformation. The large T antigen is necessary for the initiation of viral DNA synthesis, repression of transcription of the early region and is responsible in conjunction with the middle T antigen for the transformation of primary cells. Small T antigen is necessary for the completion of the productive infection cycle.
Antigens determined by leukocyte loci found on chromosome 6, the major histocompatibility loci in humans. They are polypeptides or glycoproteins found on most nucleated cells and platelets, determine tissue types for transplantation, and are associated with certain diseases.
Infections by nematodes, general or unspecified.
A subclass of segmented worms comprising the tapeworms.
Substances of fungal origin that have antigenic activity.
Differentiation antigens residing on mammalian leukocytes. CD stands for cluster of differentiation, which refers to groups of monoclonal antibodies that show similar reactivity with certain subpopulations of antigens of a particular lineage or differentiation stage. The subpopulations of antigens are also known by the same CD designation.
Determination of parasite eggs in feces.
The major group of transplantation antigens in the mouse.
A benzimidazole broad-spectrum anthelmintic structurally related to MEBENDAZOLE that is effective against many diseases. (From Martindale, The Extra Pharmacopoeia, 30th ed, p38)
A glycoprotein that is secreted into the luminal surface of the epithelia in the gastrointestinal tract. It is found in the feces and pancreaticobiliary secretions and is used to monitor the response to colon cancer treatment.
Those proteins recognized by antibodies from serum of animals bearing tumors induced by viruses; these proteins are presumably coded for by the nucleic acids of the same viruses that caused the neoplastic transformation.
A species of trematode blood flukes of the family Schistosomatidae. It is common in the Nile delta. The intermediate host is the planorbid snail. This parasite causes schistosomiasis mansoni and intestinal bilharziasis.
A superfamily of nematodes of the suborder SPIRURINA. Its organisms possess a filiform body and a mouth surrounded by papillae.
A subclass of HLA-D antigens that consist of alpha and beta chains. The inheritance of HLA-DR antigens differs from that of the HLA-DQ ANTIGENS and HLA-DP ANTIGENS.
Molecules on the surface of T-lymphocytes that recognize and combine with antigens. The receptors are non-covalently associated with a complex of several polypeptides collectively called CD3 antigens (ANTIGENS, CD3). Recognition of foreign antigen and the major histocompatibility complex is accomplished by a single heterodimeric antigen-receptor structure, composed of either alpha-beta (RECEPTORS, ANTIGEN, T-CELL, ALPHA-BETA) or gamma-delta (RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA) chains.
A genus of trematode flukes belonging to the family Schistosomatidae. There are over a dozen species. These parasites are found in man and other mammals. Snails are the intermediate hosts.
Infections with unicellular organisms formerly members of the subkingdom Protozoa.
Antibodies produced by a single clone of cells.
Inbred BALB/c mice are a strain of laboratory mice that have been selectively bred to be genetically identical to each other, making them useful for scientific research and experiments due to their consistent genetic background and predictable responses to various stimuli or treatments.
A group of antigens that includes both the major and minor histocompatibility antigens. The former are genetically determined by the major histocompatibility complex. They determine tissue type for transplantation and cause allograft rejections. The latter are systems of allelic alloantigens that can cause weak transplant rejection.
Schistosomiasis caused by Schistosoma mansoni. It is endemic in Africa, the Middle East, South America, and the Caribbean and affects mainly the bowel, spleen, and liver.
Nuclear antigen with a role in DNA synthesis, DNA repair, and cell cycle progression. PCNA is required for the coordinated synthesis of both leading and lagging strands at the replication fork during DNA replication. PCNA expression correlates with the proliferation activity of several malignant and non-malignant cell types.
Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States.
Infections with true tapeworms of the helminth subclass CESTODA.
Sites on an antigen that interact with specific antibodies.
A trisaccharide antigen expressed on glycolipids and many cell-surface glycoproteins. In the blood the antigen is found on the surface of NEUTROPHILS; EOSINOPHILS; and MONOCYTES. In addition, CD15 antigen is a stage-specific embryonic antigen.
Large, transmembrane, non-covalently linked glycoproteins (alpha and beta). Both chains can be polymorphic although there is more structural variation in the beta chains. The class II antigens in humans are called HLA-D ANTIGENS and are coded by a gene on chromosome 6. In mice, two genes named IA and IE on chromosome 17 code for the H-2 antigens. The antigens are found on B-lymphocytes, macrophages, epidermal cells, and sperm and are thought to mediate the competence of and cellular cooperation in the immune response. The term IA antigens used to refer only to the proteins encoded by the IA genes in the mouse, but is now used as a generic term for any class II histocompatibility antigen.
Excrement from the INTESTINES, containing unabsorbed solids, waste products, secretions, and BACTERIA of the DIGESTIVE SYSTEM.
The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B.
A glycoprotein that is a kallikrein-like serine proteinase and an esterase, produced by epithelial cells of both normal and malignant prostate tissue. It is an important marker for the diagnosis of prostate cancer.
The lipopolysaccharide-protein somatic antigens, usually from gram-negative bacteria, important in the serological classification of enteric bacilli. The O-specific chains determine the specificity of the O antigens of a given serotype. O antigens are the immunodominant part of the lipopolysaccharide molecule in the intact bacterial cell. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
A genus of intestinal nematode parasites belonging to the superfamily HELIGMOSOMATOIDEA, which commonly occurs in rats but has been experimentally transmitted to other rodents and rabbits. Infection is usually through the skin.
IMMUNOGLOBULINS on the surface of B-LYMPHOCYTES. Their MESSENGER RNA contains an EXON with a membrane spanning sequence, producing immunoglobulins in the form of type I transmembrane proteins as opposed to secreted immunoglobulins (ANTIBODIES) which do not contain the membrane spanning segment.
Infections with nematodes of the superfamily FILARIOIDEA. The presence of living worms in the body is mainly asymptomatic but the death of adult worms leads to granulomatous inflammation and permanent fibrosis. Organisms of the genus Elaeophora infect wild elk and domestic sheep causing ischemic necrosis of the brain, blindness, and dermatosis of the face.
Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen.
An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
Class of parasitic flukes consisting of three subclasses, Monogenea, Aspidogastrea, and Digenea. The digenetic trematodes are the only ones found in man. They are endoparasites and require two hosts to complete their life cycle.
Carbohydrate antigens expressed by malignant tissue. They are useful as tumor markers and are measured in the serum by means of a radioimmunoassay employing monoclonal antibodies.
A specific HLA-A surface antigen subtype. Members of this subtype contain alpha chains that are encoded by the HLA-A*02 allele family.
A species of helminth commonly called the sheep liver fluke. It occurs in the biliary passages, liver, and gallbladder during various stages of development. Snails and aquatic vegetation are the intermediate hosts. Occasionally seen in man, it is most common in sheep and cattle.
Differentiation antigens found on thymocytes and on cytotoxic and suppressor T-lymphocytes. CD8 antigens are members of the immunoglobulin supergene family and are associative recognition elements in MHC (Major Histocompatibility Complex) Class I-restricted interactions.
The relationship between an invertebrate and another organism (the host), one of which lives at the expense of the other. Traditionally excluded from definition of parasites are pathogenic BACTERIA; FUNGI; VIRUSES; and PLANTS; though they may live parasitically.
Subset of helper-inducer T-lymphocytes which synthesize and secrete the interleukins IL-4, IL-5, IL-6, and IL-10. These cytokines influence B-cell development and antibody production as well as augmenting humoral responses.
Deoxyribonucleic acid that makes up the genetic material of helminths.
Serological reactions in which an antiserum against one antigen reacts with a non-identical but closely related antigen.
A common parasite of humans in the moist tropics and subtropics. These organisms attach to villi in the small intestine and suck blood causing diarrhea, anorexia, and anemia.
Infections caused by infestation with worms of the class Trematoda.
Sets of cell surface antigens located on BLOOD CELLS. They are usually membrane GLYCOPROTEINS or GLYCOLIPIDS that are antigenically distinguished by their carbohydrate moieties.
Those hepatitis B antigens found on the surface of the Dane particle and on the 20 nm spherical and tubular particles. Several subspecificities of the surface antigen are known. These were formerly called the Australia antigen.
Complex of at least five membrane-bound polypeptides in mature T-lymphocytes that are non-covalently associated with one another and with the T-cell receptor (RECEPTORS, ANTIGEN, T-CELL). The CD3 complex includes the gamma, delta, epsilon, zeta, and eta chains (subunits). When antigen binds to the T-cell receptor, the CD3 complex transduces the activating signals to the cytoplasm of the T-cell. The CD3 gamma and delta chains (subunits) are separate from and not related to the gamma/delta chains of the T-cell receptor (RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA).
Morphologic alteration of small B LYMPHOCYTES or T LYMPHOCYTES in culture into large blast-like cells able to synthesize DNA and RNA and to divide mitotically. It is induced by INTERLEUKINS; MITOGENS such as PHYTOHEMAGGLUTININS, and by specific ANTIGENS. It may also occur in vivo as in GRAFT REJECTION.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
The unconsolidated mineral or organic matter on the surface of the earth that serves as a natural medium for the growth of land plants.
Polymorphic class I human histocompatibility (HLA) surface antigens present on almost all nucleated cells. At least 20 antigens have been identified which are encoded by the A locus of multiple alleles on chromosome 6. They serve as targets for T-cell cytolytic responses and are involved with acceptance or rejection of tissue/organ grafts.
A class of unsegmented helminths with fundamental bilateral symmetry and secondary triradiate symmetry of the oral and esophageal structures. Many species are parasites.
Infections or infestations with parasitic organisms. They are often contracted through contact with an intermediate vector, but may occur as the result of direct exposure.
A genus of large tapeworms.
A parasite of carnivorous mammals that causes TRICHINELLOSIS. It is especially common in rats and in swine fed uncooked garbage. Human infection is initiated by the consumption of raw or insufficiently cooked pork or other meat containing the encysted larvae.
Membrane glycoproteins consisting of an alpha subunit and a BETA 2-MICROGLOBULIN beta subunit. In humans, highly polymorphic genes on CHROMOSOME 6 encode the alpha subunits of class I antigens and play an important role in determining the serological specificity of the surface antigen. Class I antigens are found on most nucleated cells and are generally detected by their reactivity with alloantisera. These antigens are recognized during GRAFT REJECTION and restrict cell-mediated lysis of virus-infected cells.
The study of parasites and PARASITIC DISEASES.
A species of parasitic nematode widely distributed in tropical and subtropical countries. The females and their larvae inhabit the mucosa of the intestinal tract, where they cause ulceration and diarrhea.
Human immune-response or Class II antigens found mainly, but not exclusively, on B-lymphocytes and produced from genes of the HLA-D locus. They are extremely polymorphic families of glycopeptides, each consisting of two chains, alpha and beta. This group of antigens includes the -DR, -DQ and -DP designations, of which HLA-DR is most studied; some of these glycoproteins are associated with certain diseases, possibly of immune etiology.
Inbred C57BL mice are a strain of laboratory mice that have been produced by many generations of brother-sister matings, resulting in a high degree of genetic uniformity and homozygosity, making them widely used for biomedical research, including studies on genetics, immunology, cancer, and neuroscience.
The property of antibodies which enables them to react with some ANTIGENIC DETERMINANTS and not with others. Specificity is dependent on chemical composition, physical forces, and molecular structure at the binding site.
Molecules on the surface of B- and T-lymphocytes that recognize and combine with specific antigens.
The production of ANTIBODIES by proliferating and differentiated B-LYMPHOCYTES under stimulation by ANTIGENS.
High-molecular weight glycoproteins uniquely expressed on the surface of LEUKOCYTES and their hemopoietic progenitors. They contain a cytoplasmic protein tyrosine phosphatase activity which plays a role in intracellular signaling from the CELL SURFACE RECEPTORS. The CD45 antigens occur as multiple isoforms that result from alternative mRNA splicing and differential usage of three exons.
Antigens of the virion of the HEPATITIS B VIRUS or the Dane particle, its surface (HEPATITIS B SURFACE ANTIGENS), core (HEPATITIS B CORE ANTIGENS), and other associated antigens, including the HEPATITIS B E ANTIGENS.
A genus of nematodes of the superfamily ASCARIDOIDEA whose species usually inhabit the intestine.
Infection with tapeworms of the genus Hymenolepis.
55-kDa antigens found on HELPER-INDUCER T-LYMPHOCYTES and on a variety of other immune cell types. CD4 antigens are members of the immunoglobulin supergene family and are implicated as associative recognition elements in MAJOR HISTOCOMPATIBILITY COMPLEX class II-restricted immune responses. On T-lymphocytes they define the helper/inducer subset. CD4 antigens also serve as INTERLEUKIN-15 receptors and bind to the HIV receptors, binding directly to the HIV ENVELOPE PROTEIN GP120.
An immunoglobulin associated with MAST CELLS. Overexpression has been associated with allergic hypersensitivity (HYPERSENSITIVITY, IMMEDIATE).
Deliberate stimulation of the host's immune response. ACTIVE IMMUNIZATION involves administration of ANTIGENS or IMMUNOLOGIC ADJUVANTS. PASSIVE IMMUNIZATION involves administration of IMMUNE SERA or LYMPHOCYTES or their extracts (e.g., transfer factor, immune RNA) or transplantation of immunocompetent cell producing tissue (thymus or bone marrow).
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Lymphoid cells concerned with humoral immunity. They are short-lived cells resembling bursa-derived lymphocytes of birds in their production of immunoglobulin upon appropriate stimulation.
The processes triggered by interactions of ANTIBODIES with their ANTIGENS.
Glycoproteins expressed on cortical thymocytes and on some dendritic cells and B-cells. Their structure is similar to that of MHC Class I and their function has been postulated as similar also. CD1 antigens are highly specific markers for human LANGERHANS CELLS.
Infection of humans or animals with hookworms of the genus NECATOR. The resulting anemia from this condition is less severe than that from ANCYLOSTOMIASIS.
Test for tissue antigen using either a direct method, by conjugation of antibody with fluorescent dye (FLUORESCENT ANTIBODY TECHNIQUE, DIRECT) or an indirect method, by formation of antigen-antibody complex which is then labeled with fluorescein-conjugated anti-immunoglobulin antibody (FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT). The tissue is then examined by fluorescence microscopy.
Immunoglobulins produced in a response to BACTERIAL ANTIGENS.
Serum that contains antibodies. It is obtained from an animal that has been immunized either by ANTIGEN injection or infection with microorganisms containing the antigen.
Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea.
Class I human histocompatibility (HLA) surface antigens encoded by more than 30 detectable alleles on locus B of the HLA complex, the most polymorphic of all the HLA specificities. Several of these antigens (e.g., HLA-B27, -B7, -B8) are strongly associated with predisposition to rheumatoid and other autoimmune disorders. Like other class I HLA determinants, they are involved in the cellular immune reactivity of cytolytic T lymphocytes.
Specialized cells of the hematopoietic system that have branch-like extensions. They are found throughout the lymphatic system, and in non-lymphoid tissues such as SKIN and the epithelia of the intestinal, respiratory, and reproductive tracts. They trap and process ANTIGENS, and present them to T-CELLS, thereby stimulating CELL-MEDIATED IMMUNITY. They are different from the non-hematopoietic FOLLICULAR DENDRITIC CELLS, which have a similar morphology and immune system function, but with respect to humoral immunity (ANTIBODY PRODUCTION).
A superfamily of strongyles or roundworms which are parasites in the intestinal tract of equines, pigs, rodents, and primates (including man). It includes the genera Cyasthostomum, Ransomus, Globocephalus, OESOPHAGOSTOMUM, and STRONGYLUS.
Antigens expressed primarily on the membranes of living cells during sequential stages of maturation and differentiation. As immunologic markers they have high organ and tissue specificity and are useful as probes in studies of normal cell development as well as neoplastic transformation.
An infection with TRICHINELLA. It is caused by eating raw or undercooked meat that is infected with larvae of nematode worms TRICHINELLA genus. All members of the TRICHINELLA genus can infect human in addition to TRICHINELLA SPIRALIS, the traditional etiological agent. It is distributed throughout much of the world and is re-emerging in some parts as a public health hazard and a food safety problem.
Established cell cultures that have the potential to propagate indefinitely.
A benzimidazole that acts by interfering with CARBOHYDRATE METABOLISM and inhibiting polymerization of MICROTUBULES.
The genetic complement of a helminth (HELMINTHS) as represented in its DNA.
The total number of cases of a given disease in a specified population at a designated time. It is differentiated from INCIDENCE, which refers to the number of new cases in the population at a given time.
A melanosome-specific protein that plays a role in the expression, stability, trafficking, and processing of GP100 MELANOMA ANTIGEN, which is critical to the formation of Stage II MELANOSOMES. The protein is used as an antigen marker for MELANOMA cells.
An encapsulated lymphatic organ through which venous blood filters.
The major interferon produced by mitogenically or antigenically stimulated LYMPHOCYTES. It is structurally different from TYPE I INTERFERON and its major activity is immunoregulation. It has been implicated in the expression of CLASS II HISTOCOMPATIBILITY ANTIGENS in cells that do not normally produce them, leading to AUTOIMMUNE DISEASES.
Drugs used to treat or prevent parasitic infections.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Infection with tapeworms of the genus Taenia.
The smallest species of TAPEWORMS. It is the only cestode that parasitizes humans without requiring an intermediate host.
An anthelmintic used in most schistosome and many cestode infestations.
A species of parasitic nematode usually found in domestic pigs and a few other animals. Human infection can also occur, presumably as result of handling pig manure, and can lead to intestinal obstruction.
Antigens associated with specific proteins of the human adult T-cell immunodeficiency virus (HIV); also called HTLV-III-associated and lymphadenopathy-associated virus (LAV) antigens.
Invertebrate organisms that live on or in another organism (the host), and benefit at the expense of the other. Traditionally excluded from definition of parasites are pathogenic BACTERIA; FUNGI; VIRUSES; and PLANTS; though they may live parasitically.
A costimulatory ligand expressed by ANTIGEN-PRESENTING CELLS that binds to CTLA-4 ANTIGEN with high specificity and to CD28 ANTIGEN with low specificity. The interaction of CD80 with CD28 ANTIGEN provides a costimulatory signal to T-LYMPHOCYTES, while its interaction with CTLA-4 ANTIGEN may play a role in inducing PERIPHERAL TOLERANCE.
Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA.
Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake.
A genus of nematode intestinal parasites that consists of several species. A. duodenale is the common hookworm in humans. A. braziliense, A. ceylonicum, and A. caninum occur primarily in cats and dogs, but all have been known to occur in humans.
An albumin obtained from the white of eggs. It is a member of the serpin superfamily.
Non-antibody proteins secreted by inflammatory leukocytes and some non-leukocytic cells, that act as intercellular mediators. They differ from classical hormones in that they are produced by a number of tissue or cell types rather than by specialized glands. They generally act locally in a paracrine or autocrine rather than endocrine manner.
Simultaneous infection of a host organism by two or more pathogens. In virology, coinfection commonly refers to simultaneous infection of a single cell by two or more different viruses.
Nuclear antigens encoded by VIRAL GENES found in HUMAN HERPESVIRUS 4. At least six nuclear antigens have been identified.
A species of trematode blood flukes of the family Schistosomatidae which occurs at different stages in development in veins of the pulmonary and hepatic system and finally the bladder lumen. This parasite causes urinary schistosomiasis.
Immunologic techniques based on the use of: (1) enzyme-antibody conjugates; (2) enzyme-antigen conjugates; (3) antienzyme antibody followed by its homologous enzyme; or (4) enzyme-antienzyme complexes. These are used histologically for visualizing or labeling tissue specimens.
A critical subpopulation of T-lymphocytes involved in the induction of most immunological functions. The HIV virus has selective tropism for the T4 cell which expresses the CD4 phenotypic marker, a receptor for HIV. In fact, the key element in the profound immunosuppression seen in HIV infection is the depletion of this subset of T-lymphocytes.
Manifestations of the immune response which are mediated by antigen-sensitized T-lymphocytes via lymphokines or direct cytotoxicity. This takes place in the absence of circulating antibody or where antibody plays a subordinate role.
Differentiation antigens expressed on B-lymphocytes and B-cell precursors. They are involved in regulation of B-cell proliferation.
A heterogeneous group of immunocompetent cells that mediate the cellular immune response by processing and presenting antigens to the T-cells. Traditional antigen-presenting cells include MACROPHAGES; DENDRITIC CELLS; LANGERHANS CELLS; and B-LYMPHOCYTES. FOLLICULAR DENDRITIC CELLS are not traditional antigen-presenting cells, but because they hold antigen on their cell surface in the form of IMMUNE COMPLEXES for B-cell recognition they are considered so by some authors.
A white threadlike worm which causes elephantiasis, lymphangitis, and chyluria by interfering with the lymphatic circulation. The microfilaria are found in the circulating blood and are carried by mosquitoes.
A soluble factor produced by activated T-LYMPHOCYTES that induces the expression of MHC CLASS II GENES and FC RECEPTORS on B-LYMPHOCYTES and causes their proliferation and differentiation. It also acts on T-lymphocytes, MAST CELLS, and several other hematopoietic lineage cells.
Antigens stimulating the formation of, or combining with heterophile antibodies. They are cross-reacting antigens found in phylogenetically unrelated species.
Infection by round worms of the genus TOXOCARA, usually found in wild and domesticated cats and dogs and foxes, except for the larvae, which may produce visceral and ocular larva migrans in man.
The hepatitis B antigen within the core of the Dane particle, the infectious hepatitis virion.
A genus of small tapeworms of birds and mammals.
A member of the tumor necrosis factor receptor superfamily with specificity for CD40 LIGAND. It is found on mature B-LYMPHOCYTES and some EPITHELIAL CELLS, lymphoid DENDRITIC CELLS. Evidence suggests that CD40-dependent activation of B-cells is important for generation of memory B-cells within the germinal centers. Mutations of the gene for CD40 antigen result in HYPER-IGM IMMUNODEFICIENCY SYNDROME, TYPE 3. Signaling of the receptor occurs through its association with TNF RECEPTOR-ASSOCIATED FACTORS.
Technique involving the diffusion of antigen or antibody through a semisolid medium, usually agar or agarose gel, with the result being a precipitin reaction.
Endogenous tissue constituents that have the ability to interact with AUTOANTIBODIES and cause an immune response.
Granular leukocytes characterized by a relatively pale-staining, lobate nucleus and cytoplasm containing coarse dark-staining granules of variable size and stainable by basic dyes.
Immunoglobulin molecules having a specific amino acid sequence by virtue of which they interact only with the ANTIGEN (or a very similar shape) that induced their synthesis in cells of the lymphoid series (especially PLASMA CELLS).
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
A republic in western Africa, south of MALI and BURKINA FASO, bordered by GHANA on the east. Its administrative capital is Abidjan and Yamoussoukro has been the official capital since 1983. The country was formerly called Ivory Coast.
A class of immunoglobulin bearing mu chains (IMMUNOGLOBULIN MU-CHAINS). IgM can fix COMPLEMENT. The name comes from its high molecular weight and originally being called a macroglobulin.
Infection with nematodes of the genus MANSONELLA. Symptoms include pruritus, headache, and articular swelling.
A group of differentiation surface antigens, among the first to be discovered on thymocytes and T-lymphocytes. Originally identified in the mouse, they are also found in other species including humans, and are expressed on brain neurons and other cells.
A glycolipid, cross-species antigen that induces production of antisheep hemolysin. It is present on the tissue cells of many species but absent in humans. It is found in many infectious agents.
The complex formed by the binding of antigen and antibody molecules. The deposition of large antigen-antibody complexes leading to tissue damage causes IMMUNE COMPLEX DISEASES.
A superfamily of parasitic nematodes which requires one or two intermediate arthropod hosts before finally being eaten by the final host. Its organisms occur rarely in man.
A sex-specific cell surface antigen produced by the sex-determining gene of the Y chromosome in mammals. It causes syngeneic grafts from males to females to be rejected and interacts with somatic elements of the embryologic undifferentiated gonad to produce testicular organogenesis.
Suspensions of killed or attenuated microorganisms (bacteria, viruses, fungi, protozoa), antigenic proteins, synthetic constructs, or other bio-molecular derivatives, administered for the prevention, amelioration, or treatment of infectious and other diseases.
A human disease caused by the infection of parasitic worms SCHISTOSOMA HAEMATOBIUM. It is endemic in AFRICA and parts of the MIDDLE EAST. Tissue damages most often occur in the URINARY TRACT, specifically the URINARY BLADDER.
The sum of the weight of all the atoms in a molecule.
White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS.
Serologic tests based on inactivation of complement by the antigen-antibody complex (stage 1). Binding of free complement can be visualized by addition of a second antigen-antibody system such as red cells and appropriate red cell antibody (hemolysin) requiring complement for its completion (stage 2). Failure of the red cells to lyse indicates that a specific antigen-antibody reaction has taken place in stage 1. If red cells lyse, free complement is present indicating no antigen-antibody reaction occurred in stage 1.
A group of the D-related HLA antigens found to differ from the DR antigens in genetic locus and therefore inheritance. These antigens are polymorphic glycoproteins comprising alpha and beta chains and are found on lymphoid and other cells, often associated with certain diseases.
A costimulatory ligand expressed by ANTIGEN-PRESENTING CELLS that binds to CD28 ANTIGEN with high specificity and to CTLA-4 ANTIGEN with low specificity. The interaction of CD86 with CD28 ANTIGEN provides a stimulatory signal to T-LYMPHOCYTES, while its interaction with CTLA-4 ANTIGEN may play a role in inducing PERIPHERAL TOLERANCE.
A species of POLYOMAVIRUS originally isolated from Rhesus monkey kidney tissue. It produces malignancy in human and newborn hamster kidney cell cultures.
Proteins prepared by recombinant DNA technology.
A genus of parasitic nematodes widely distributed as intestinal parasites of mammals.
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)
The specific failure of a normally responsive individual to make an immune response to a known antigen. It results from previous contact with the antigen by an immunologically immature individual (fetus or neonate) or by an adult exposed to extreme high-dose or low-dose antigen, or by exposure to radiation, antimetabolites, antilymphocytic serum, etc.
Immunized T-lymphocytes which can directly destroy appropriate target cells. These cytotoxic lymphocytes may be generated in vitro in mixed lymphocyte cultures (MLC), in vivo during a graft-versus-host (GVH) reaction, or after immunization with an allograft, tumor cell or virally transformed or chemically modified target cell. The lytic phenomenon is sometimes referred to as cell-mediated lympholysis (CML). These CD8-positive cells are distinct from NATURAL KILLER CELLS and NATURAL KILLER T-CELLS. There are two effector phenotypes: TC1 and TC2.
Infection by flukes of the genus Echinostoma.
Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations, or by parent x offspring matings carried out with certain restrictions. All animals within an inbred strain trace back to a common ancestor in the twentieth generation.
Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen.
A species of trematode blood flukes belonging to the family Schistosomatidae whose distribution is confined to areas of the Far East. The intermediate host is a snail. It occurs in man and other mammals.
T-cell receptors composed of CD3-associated alpha and beta polypeptide chains and expressed primarily in CD4+ or CD8+ T-cells. Unlike immunoglobulins, the alpha-beta T-cell receptors recognize antigens only when presented in association with major histocompatibility (MHC) molecules.
A species of parasitic nematode found in the intestine of dogs. Lesions in the brain, liver, eye, kidney, and lung are caused by migrating larvae. In humans, these larvae do not follow normal patterns and may produce visceral larva migrans (LARVA MIGRANS, VISCERAL).
The species Oryctolagus cuniculus, in the family Leporidae, order LAGOMORPHA. Rabbits are born in burrows, furless, and with eyes and ears closed. In contrast with HARES, rabbits have 22 chromosome pairs.
Parasitic infestation of the human lymphatic system by WUCHERERIA BANCROFTI or BRUGIA MALAYI. It is also called lymphatic filariasis.
A mixture of mostly avermectin H2B1a (RN 71827-03-7) with some avermectin H2B1b (RN 70209-81-3), which are macrolides from STREPTOMYCES avermitilis. It binds glutamate-gated chloride channel to cause increased permeability and hyperpolarization of nerve and muscle cells. It also interacts with other CHLORIDE CHANNELS. It is a broad spectrum antiparasitic that is active against microfilariae of ONCHOCERCA VOLVULUS but not the adult form.
Immunoglobulins produced in response to VIRAL ANTIGENS.
A technique that combines protein electrophoresis and double immunodiffusion. In this procedure proteins are first separated by gel electrophoresis (usually agarose), then made visible by immunodiffusion of specific antibodies. A distinct elliptical precipitin arc results for each protein detectable by the antisera.
Infections or infestations with parasitic organisms. The infestation may be experimental or veterinary.
An inhibitory T CELL receptor that is closely related to CD28 ANTIGEN. It has specificity for CD80 ANTIGEN and CD86 ANTIGEN and acts as a negative regulator of peripheral T cell function. CTLA-4 antigen is believed to play role in inducing PERIPHERAL TOLERANCE.
A critical subpopulation of regulatory T-lymphocytes involved in MHC Class I-restricted interactions. They include both cytotoxic T-lymphocytes (T-LYMPHOCYTES, CYTOTOXIC) and CD8+ suppressor T-lymphocytes.
Substances used in the treatment or control of nematode infestations. They are used also in veterinary practice.
The science dealing with the establishment and maintenance of health in the individual and the group. It includes the conditions and practices conducive to health. (Webster, 3d ed)
A supergroup (some say phylum) of ameboid EUKARYOTES, comprising ARCHAMOEBAE; LOBOSEA; and MYCETOZOA.
Infection with nematodes of the genus ONCHOCERCA. Characteristics include the presence of firm subcutaneous nodules filled with adult worms, PRURITUS, and ocular lesions.
Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA).
A component of the B-cell antigen receptor that is involved in B-cell antigen receptor heavy chain transport to the PLASMA MEMBRANE. It is expressed almost exclusively in B-LYMPHOCYTES and serves as a useful marker for B-cell NEOPLASMS.
Immunoglobulins produced in a response to PROTOZOAN ANTIGENS.
They are oval or bean shaped bodies (1 - 30 mm in diameter) located along the lymphatic system.
Sialylated Lewis blood group carbohydrate antigen found in many adenocarcinomas of the digestive tract, especially pancreatic tumors.
Strains of mice in which certain GENES of their GENOMES have been disrupted, or "knocked-out". To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product. Cloned cells in which this DNA alteration is successful are then injected into mouse EMBRYOS to produce chimeric mice. The chimeric mice are then bred to yield a strain in which all the cells of the mouse contain the disrupted gene. Knockout mice are used as EXPERIMENTAL ANIMAL MODELS for diseases (DISEASE MODELS, ANIMAL) and to clarify the functions of the genes.
Infection of humans or animals with hookworms of the genus ANCYLOSTOMA. Characteristics include anemia, dyspepsia, eosinophilia, and abdominal swelling.
Laboratory mice that have been produced from a genetically manipulated EGG or EMBRYO, MAMMALIAN.
The co-occurrence of pregnancy and parasitic diseases. The parasitic infection may precede or follow FERTILIZATION.
Subset of helper-inducer T-lymphocytes which synthesize and secrete interleukin-2, gamma-interferon, and interleukin-12. Due to their ability to kill antigen-presenting cells and their lymphokine-mediated effector activity, Th1 cells are associated with vigorous delayed-type hypersensitivity reactions.
Sensitive tests to measure certain antigens, antibodies, or viruses, using their ability to agglutinate certain erythrocytes. (From Stedman, 26th ed)
A melanosome-associated protein that plays a role in the maturation of the MELANOSOME.
Diagnostic procedures involving immunoglobulin reactions.
A group of dominantly and independently inherited antigens associated with the ABO blood factors. They are glycolipids present in plasma and secretions that may adhere to the erythrocytes. The phenotype Le(b) is the result of the interaction of the Le gene Le(a) with the genes for the ABO blood groups.
I'm sorry for any confusion, but "Laos" is not a medical term; it is the name of a country located in Southeast Asia, officially known as the Lao People's Democratic Republic. If you have any questions related to medical terminology or health-related topics, I would be happy to help with those!
A CELL CYCLE and tumor growth marker which can be readily detected using IMMUNOCYTOCHEMISTRY methods. Ki-67 is a nuclear antigen present only in the nuclei of cycling cells.

Differential serodiagnosis for cystic and alveolar echinococcosis using fractions of Echinococcus granulosus cyst fluid (antigen B) and E. multilocularis protoscolex (EM18). (1/1434)

Echinococcus granulosus cyst fluid and E. multilocularis protoscolex extract were fractionated by a single step of preparative isoelectric focusing, resulting in an antigen B-rich fraction (8-kD) and an Em18-rich fraction, respectively. The usefulness of both fractions for differential serodiagnosis of cystic (CE) and alveolar (AE) echinococcosis was evaluated by a large-scale immunoblot analysis on a battery of 354 serum samples. These included 66 from AE patients originating from four different endemic areas, 173 from CE patients originating from seven different endemic areas, 71 from patients with other parasitic diseases, 15 from patients with hepatomas, and 29 from healthy individuals. In an immunoblot with the antigen B-rich fraction, 92% (158 of 173) of the CE sera as well as 79% (52 of 66) of the AE sera reacted with the 8-kD subunit. No cross-reactivity occurred with any sera from patients with cysticercosis, other parasitic diseases, or with hepatomas, or from healthy controls. In an immunoblot with the Em18-rich fraction, all but two sera from AE patients (64 of 66, 97%) recognized Em18, and only nine of 34 CE sera from China reacted with it. All other (139) CE sera from six other countries were negative as were all (115) other non-echinococcosis sera. These findings indicate that antigen B (8-kD) is not species-specific for E. granulosus but is genus-specific for Echinococcus, and that the Em18 antigen is a reliable serologic marker for species-specific differentiation of AE from CE.  (+info)

Development of a serologic assay to detect Taenia solium taeniasis. (2/1434)

We developed a serologic assay to identify adult Taenia solium tapeworm carriers using excretory/secretory (TSES) antigens collected from in vitro cultured T. solium tapeworms. To identify taeniasis-specific antigens we used an immunoblot assay with serum samples from T. solium tapeworm carriers and cysticercosis patients. Antigens were identified that reacted with antibodies present in serum samples from taeniasis cases and not with those from cysticercosis patients. Using serum samples collected from persons with confirmed T. solium tapeworm infections, the test was determined to be 95% (69 of 73) sensitive. Serum samples (n = 193) from persons with other parasitic infections, including T. saginata tapeworm infections, do not contain cross-reacting antibodies to TSES, indicating that the assay is 100% specific. These data suggest that the immunoblot assay using TSES antigens can be used to identify persons with current or recent T. solium tapeworm infections and provides a new, important tool for epidemiologic purposes, including control and prevention strategies.  (+info)

Granulomatous inflammatory response to recombinant filarial proteins of Brugia species. (3/1434)

The lymphatic inflammatory response in Brugia-infected jirds peaks early during primary infections and then decreases in severity as judged by the numbers of lymph thrombi present within these vessels. Antigen-specific hypersensitivity reactions in these animals was measured by a pulmonary granulomatous inflammatory response (PGRN) induced by somatic adult worm antigen (SAWA)-coated beads, and by cellular proliferative responses of renal lymph node cells. The kinetics of these responses temporally correspond to lymphatic lesion formation. The importance of any single antigen to the induction of this inflammatory response has not been elucidated. In this study, the PGRN was used to measure the cellular immune response to four recombinant filarial proteins during the course of a primary B. pahangi infection. These proteins were BpL4, glycoprotein (glutathione peroxidase) gp29, heat shock protein (hsp) 70, and filarial chitinase. All were fusion proteins of maltose-binding protein (MBP). Control beads included those coated with diethanolamine (DEA), SAWA, or MBP. The measurements of PRGN were made at 14, 28, 56, and > 150 days postinfection (PI) in infected jirds, in jirds sensitized with SAWA, and in uninfected jirds. The secretory homolog of glutathione peroxidase gp29 was the only recombinant protein tested that induced a significantly greater PGRN (P < 0.05) than controls. This was seen at 28 days PI. These observations indicate that gp29 may be part of the worm antigen complex that induces an early inflammatory response, a response similar to that observed with SAWA. These studies indicate that this approach is useful in investigating the functional ability of specific proteins in the induction and down-regulation of immune-mediated inflammatory responses elicited by filarial parasites. Absence of a granulomatous response to the other recombinant proteins used may be related to the nature and sensitivity of the assay used or the character of recombinant proteins tested.  (+info)

Inhibitory effect of artemether on proteinase of Schistosoma japonicum. (4/1434)

AIM: To study the effect of artemether (Art) on the thio proteinase ("hemoglobinase", Hem) of Schistosoma japonicum. METHODS: Hem was extracted from S japonicum adults. The inhibitory effect of Art on the activity of Hem to degrade human hemoglobin (Hgb) was examined with UV-photometer at 280 nm, SDS-PAGE and scanning at 600 nm on a chromoscanner. RESULTS: Human Hgb was degraded at pH 4.0 by the Hem. The activities of Hem preincubated at 37 degrees C with Art 0.14, 1.4, and 14 mmol.L-1, were inhibited by 30.2%, 39.8%, and 45.0%, respectively. CONCLUSION: Art possesses an inhibitory effect to Hem of S japonicum.  (+info)

Interleukin-10 and antigen-presenting cells actively suppress Th1 cells in BALB/c mice infected with the filarial parasite Brugia pahangi. (5/1434)

Infection with the third-stage larvae (L3) of the filarial nematode Brugia results in a Th2-biased immune response in mice and humans. Previously we have shown that the production of interleukin 4 (IL-4) is critical for down-regulating polyclonal Th1 responses in L3-infected mice. However, the in vitro neutralization of IL-4 did not fully recover the defective polyclonal Th1 responses, nor did it result in the production of any antigen (Ag)-specific Th1 cytokines, suggesting that perhaps infection with L3 does not result in priming of Th1 cells in vivo. In this study, we analyzed the role of IL-10 and Ag-presenting cells (APCs) in the spleen as additional factors controlling the Th2 bias in infected mice. Our data show that IL-10 and APCs also contribute to the suppression of mitogen-driven Th1 responses of spleen cells from infected mice. In addition, the neutralization of IL-10 or the replacement of the resident APC population from spleen cell cultures resulted in the production of Ag-specific Th1 cytokines. Irradiated spleen cells from either L3-infected or uninfected mice were able to restore Ag-specific Th1 responses in vitro. Therefore, it appears that Brugia-reactive Th1 cells are primed following infection with L3, but are actively suppressed in vivo by a mechanism that involves IL-10 and the resident APC population, but not IL-4. These results indicate that a complex interplay of cytokines and cell populations underscores the Th2-polarized response in L3-infected mice.  (+info)

A novel 62-kilodalton egg antigen from Schistosoma mansoni induces a potent CD4(+) T helper cell response in the C57BL/6 mouse. (6/1434)

In infection with Schistosoma mansoni, hepatic granuloma formation is mediated by CD4(+) T helper (Th) cells sensitized to schistosomal egg antigens. There is considerable variation among infected individuals with respect to both severity of disease and the T-cell response to egg antigens. In the BL/6 mouse, the egg granulomas are relatively small and the relevant sensitizing egg antigens are largely unknown. We investigated the CD4(+) Th cell response of infected BL/6 mice to egg antigens fractionated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and found a prominent lymphoproliferative response to be directed against a 62-kDa component. With the aid of a specific T-cell hybridoma, 4E6, the 62-kDa antigen was isolated; following partial digestion with endoproteinase Glu-C, an internal amino acid sequence was found to be identical with one present in the enzyme phosphoenolpyruvate carboxykinase (PEPCK) of the organisms Caenorhabditis elegans and Treponema pallidum and to differ by one residue from PEPCK of various other species. In CD4(+) Th cells from 7.5- 8.5-week-infected BL/6 mice, the purified 62-kDa molecule elicited a potent proliferative response which, based on cytokine analysis, was of a mixed Th-1 and Th-2 type. Our results reveal a novel egg antigen of particular prominence in the BL/6 mouse and suggest that the immune response in schistosomiasis is a product of sensitization to egg antigens that may vary considerably in immunogenicity from strain to strain.  (+info)

Vaccination with cathepsin L proteinases and with leucine aminopeptidase induces high levels of protection against fascioliasis in sheep. (7/1434)

The potential of different parasite proteinases for use as vaccine candidates against fascioliasis in sheep was studied by vaccinating animals with the cathepsin L proteinases CL1 and CL2 and with leucine aminopeptidase (LAP) purified from adult flukes. In the first trial, sheep were immunized with CL1 or CL2 and the mean protection levels obtained were 33 and 34%, respectively. Furthermore, a significant reduction in egg output was observed in sheep vaccinated either with CL1 (71%) or with CL2 (81%). The second trial was performed to determine the protective potential of the two cathepsin L proteinases assayed together, as well as in combination with LAP, and of LAP alone. The combination of CL1 and CL2 induced higher levels of protection (60%) than those produced when these enzymes were administered separately. Those sheep that received the cocktail vaccine including CL1, CL2, and LAP were significantly protected (78%) against metacercarial challenge, but vaccination with LAP alone elicited the highest level of protection (89%). All vaccine preparations induced high immunoglobulin G titers which were boosted after the challenge infection, but no correlations between antibody titers and worm burdens were found. However, the sera of those animals vaccinated with LAP contained LAP-neutralizing antibodies. Reduced liver damage, as assessed by the level of the liver enzyme gamma-glutamyl transferase, was observed in the groups vaccinated with CL1, CL2, and LAP or with LAP alone.  (+info)

Tolerization of mice to Schistosoma mansoni egg antigens causes elevated type 1 and diminished type 2 cytokine responses and increased mortality in acute infection. (8/1434)

The granuloma that surrounds the Schistosoma mansoni egg is the cause of pathology in murine schistosomiasis, and its formation is driven by egg Ag-stimulated type 1 and type 2 cytokines. To determine the role of egg-driven immune responses during schistosome infection we rendered CBA/Ca mice unresponsive to schistosome eggs by combined cyclophosphamide treatment and thymectomy. In the early acute stages of schistosome infection, egg-tolerized mice suffered high mortalities. Granuloma size and deposition of collagen in the liver were significantly reduced in egg-tolerized mice. Similarly, limited granuloma responses were detected in the intestines of these mice, and this was associated with a >90% reduction in egg excretion. Histologically, egg-tolerized mice had exacerbated hepatocyte damage, with extensive microvesicular steatosis. Elevated plasma transaminase levels confirmed the damage to hepatocytes. Infected egg-tolerized mice had impaired proliferation responses to egg Ag but intact responses to worm Ag. Tolerized mice had diminished Ab responses to egg Ag and had a type 1 cytokine isotype pattern to worm Ag, with elevated IgG2a and diminished IgG1 and IgE. Egg-tolerized mice failed to down-regulate type 1 cytokines that are normally elicited during early schistosome infection. Hepatic granuloma cells from egg-tolerized mice were also type 1 cytokine dominated, with elevated frequencies of Tc1/Th1 and reduced Tc2/Th2 cells. This study demonstrates that mice tolerized to schistosome eggs have elevated type 1 cytokine responses with diminished type 2 responses and reduced anti-egg Ab during schistosome infection, and these effects are detrimental to the host.  (+info)

Helminths are a type of parasitic worm that can infect humans and animals. They are multi-cellular organisms that belong to the phyla Platyhelminthes (flatworms) or Nematoda (roundworms). Helminths can be further classified into three main groups: nematodes (roundworms), cestodes (tapeworms), and trematodes (flukes).

Helminth infections are typically acquired through contact with contaminated soil, food, or water. The symptoms of helminth infections can vary widely depending on the type of worm and the location and extent of the infection. Some common symptoms include abdominal pain, diarrhea, anemia, and malnutrition.

Helminths have complex life cycles that often involve multiple hosts. They can be difficult to diagnose and treat, and in some cases, may require long-term treatment with anti-parasitic drugs. Preventive measures such as good hygiene practices, proper sanitation, and access to clean water can help reduce the risk of helminth infections.

Helminthiasis is a medical condition characterized by the infection and infestation of body tissues and organs by helminths, which are parasitic worms. These worms can be classified into three main groups: nematodes (roundworms), cestodes (tapeworms), and trematodes (flukes).

Helminthiasis infections can occur through various modes of transmission, such as ingestion of contaminated food or water, skin contact with contaminated soil, or direct contact with an infected person or animal. The severity of the infection depends on several factors, including the type and number of worms involved, the duration of the infestation, and the overall health status of the host.

Common symptoms of helminthiasis include abdominal pain, diarrhea, nausea, vomiting, weight loss, anemia, and nutritional deficiencies. In severe cases, the infection can lead to organ damage or failure, impaired growth and development in children, and even death.

Diagnosis of helminthiasis typically involves microscopic examination of stool samples to identify the presence and type of worms. Treatment usually consists of administering anthelmintic drugs that are effective against specific types of worms. Preventive measures include improving sanitation and hygiene, avoiding contact with contaminated soil or water, and practicing safe food handling and preparation.

An antigen is a substance (usually a protein) that is recognized as foreign by the immune system and stimulates an immune response, leading to the production of antibodies or activation of T-cells. Antigens can be derived from various sources, including bacteria, viruses, fungi, parasites, and tumor cells. They can also come from non-living substances such as pollen, dust mites, or chemicals.

Antigens contain epitopes, which are specific regions on the antigen molecule that are recognized by the immune system. The immune system's response to an antigen depends on several factors, including the type of antigen, its size, and its location in the body.

In general, antigens can be classified into two main categories:

1. T-dependent antigens: These require the help of T-cells to stimulate an immune response. They are typically larger, more complex molecules that contain multiple epitopes capable of binding to both MHC class II molecules on antigen-presenting cells and T-cell receptors on CD4+ T-cells.
2. T-independent antigens: These do not require the help of T-cells to stimulate an immune response. They are usually smaller, simpler molecules that contain repetitive epitopes capable of cross-linking B-cell receptors and activating them directly.

Understanding antigens and their properties is crucial for developing vaccines, diagnostic tests, and immunotherapies.

Helminthiasis, in general, refers to the infection or infestation of humans and animals by helminths, which are parasitic worms. When referring to "Animal Helminthiasis," it specifically pertains to the condition where animals, including domestic pets and livestock, are infected by various helminth species. These parasitic worms can reside in different organs of the animal's body, leading to a wide range of clinical signs depending on the worm species and the location of the infestation.

Animal Helminthiasis can be caused by different types of helminths:

1. Nematodes (roundworms): These include species like Ascaris suum in pigs, Toxocara cati and Toxascaris leonina in cats, and Toxocara canis in dogs. They can cause gastrointestinal issues such as diarrhea, vomiting, and weight loss.
2. Cestodes (tapeworms): Examples include Taenia saginata in cattle, Echinococcus granulosus in sheep and goats, and Dipylidium caninum in dogs and cats. Tapeworm infestations may lead to gastrointestinal symptoms like diarrhea or constipation and may also cause vitamin deficiencies due to the worm's ability to absorb nutrients from the host animal's digestive system.
3. Trematodes (flukes): These include liver flukes such as Fasciola hepatica in sheep, goats, and cattle, and schistosomes that can affect various animals, including birds and mammals. Liver fluke infestations may cause liver damage, leading to symptoms like weight loss, decreased appetite, and jaundice. Schistosome infestations can lead to issues in multiple organs depending on the species involved.

Preventing and controlling Helminthiasis in animals is crucial for maintaining animal health and welfare, as well as ensuring food safety for humans who consume products from these animals. Regular deworming programs, good hygiene practices, proper pasture management, and monitoring for clinical signs are essential components of a comprehensive parasite control strategy.

Helminthic therapy, also known as helminth therapy or worm therapy, is a medical treatment that involves the intentional introduction of specially selected species of parasitic worms, known as helminths, into the human body. The goal of this therapy is to treat or alleviate various immune-mediated inflammatory disorders and autoimmune diseases by modulating the host's immune response.

The most commonly used helminths in therapeutic settings are:

1. Necator americanus (hookworm): These are intestinal parasites that adults typically acquire through contact with contaminated soil. In a therapeutic setting, a small number of larvae are introduced into the patient's skin, which then migrate to the gastrointestinal tract and establish a low-level, chronic infection.
2. Trichuris suis (pig whipworm): This is another intestinal parasite that primarily infects pigs. In helminthic therapy, patients ingest ova (eggs) of T. suis, which hatch in the small intestine and mature into adults. However, these worms cannot complete their life cycle in humans and are expelled from the body within a few weeks.

The exact mechanisms through which helminthic therapy exerts its therapeutic effects are not fully understood, but it is believed that the presence of these non-pathogenic worms helps to restore immune homeostasis by modulating the host's immune response. This includes downregulation of pro-inflammatory cytokines and an increase in anti-inflammatory cytokines, which can help alleviate symptoms associated with various autoimmune and inflammatory conditions.

Helminthic therapy is still considered an experimental treatment and is not widely available or approved by regulatory agencies for the treatment of specific medical conditions. However, clinical trials and observational studies have suggested potential benefits in treating diseases such as inflammatory bowel disease (IBD), multiple sclerosis (MS), asthma, and allergies. It is essential to consult with a healthcare professional before considering helminthic therapy, as there are potential risks and side effects associated with the treatment.

Bacterial antigens are substances found on the surface or produced by bacteria that can stimulate an immune response in a host organism. These antigens can be proteins, polysaccharides, teichoic acids, lipopolysaccharides, or other molecules that are recognized as foreign by the host's immune system.

When a bacterial antigen is encountered by the host's immune system, it triggers a series of responses aimed at eliminating the bacteria and preventing infection. The host's immune system recognizes the antigen as foreign through the use of specialized receptors called pattern recognition receptors (PRRs), which are found on various immune cells such as macrophages, dendritic cells, and neutrophils.

Once a bacterial antigen is recognized by the host's immune system, it can stimulate both the innate and adaptive immune responses. The innate immune response involves the activation of inflammatory pathways, the recruitment of immune cells to the site of infection, and the production of antimicrobial peptides.

The adaptive immune response, on the other hand, involves the activation of T cells and B cells, which are specific to the bacterial antigen. These cells can recognize and remember the antigen, allowing for a more rapid and effective response upon subsequent exposures.

Bacterial antigens are important in the development of vaccines, as they can be used to stimulate an immune response without causing disease. By identifying specific bacterial antigens that are associated with virulence or pathogenicity, researchers can develop vaccines that target these antigens and provide protection against infection.

Helminth antigens refer to the proteins or other molecules found on the surface or within helminth parasites that can stimulate an immune response in a host organism. Helminths are large, multicellular parasitic worms that can infect various tissues and organs in humans and animals, causing diseases such as schistosomiasis, lymphatic filariasis, and soil-transmitted helminthiases.

Helminth antigens can be recognized by the host's immune system as foreign invaders, leading to the activation of various immune cells and the production of antibodies. However, many helminths have evolved mechanisms to evade or suppress the host's immune response, allowing them to establish long-term infections.

Studying helminth antigens is important for understanding the immunology of helminth infections and developing new strategies for diagnosis, treatment, and prevention. Some researchers have also explored the potential therapeutic use of helminth antigens or whole helminths as a way to modulate the immune system and treat autoimmune diseases or allergies. However, more research is needed to determine the safety and efficacy of these approaches.

Parasitic intestinal diseases are disorders caused by microscopic parasites that invade the gastrointestinal tract, specifically the small intestine. These parasites include protozoa (single-celled organisms) and helminths (parasitic worms). The most common protozoan parasites that cause intestinal disease are Giardia lamblia, Cryptosporidium parvum, and Entamoeba histolytica. Common helminthic parasites include roundworms (Ascaris lumbricoides), tapeworms (Taenia saginata and Taenia solium), hookworms (Ancylostoma duodenale and Necator americanus), and pinworms (Enterobius vermicularis).

Parasitic intestinal diseases can cause a variety of symptoms, including diarrhea, abdominal pain, bloating, nausea, vomiting, fatigue, and weight loss. The severity and duration of the symptoms depend on the type of parasite, the number of organisms present, and the immune status of the host.

Transmission of these parasites can occur through various routes, including contaminated food and water, person-to-person contact, and contact with contaminated soil or feces. Preventive measures include practicing good hygiene, washing hands thoroughly after using the toilet and before handling food, cooking food thoroughly, and avoiding consumption of raw or undercooked meat, poultry, or seafood.

Treatment of parasitic intestinal diseases typically involves the use of antiparasitic medications that target the specific parasite causing the infection. In some cases, supportive care such as fluid replacement and symptom management may also be necessary.

Neoplasm antigens, also known as tumor antigens, are substances that are produced by cancer cells (neoplasms) and can stimulate an immune response. These antigens can be proteins, carbohydrates, or other molecules that are either unique to the cancer cells or are overexpressed or mutated versions of normal cellular proteins.

Neoplasm antigens can be classified into two main categories: tumor-specific antigens (TSAs) and tumor-associated antigens (TAAs). TSAs are unique to cancer cells and are not expressed by normal cells, while TAAs are present at low levels in normal cells but are overexpressed or altered in cancer cells.

TSAs can be further divided into viral antigens and mutated antigens. Viral antigens are produced when cancer is caused by a virus, such as human papillomavirus (HPV) in cervical cancer. Mutated antigens are the result of genetic mutations that occur during cancer development and are unique to each patient's tumor.

Neoplasm antigens play an important role in the immune response against cancer. They can be recognized by the immune system, leading to the activation of immune cells such as T cells and natural killer (NK) cells, which can then attack and destroy cancer cells. However, cancer cells often develop mechanisms to evade the immune response, allowing them to continue growing and spreading.

Understanding neoplasm antigens is important for the development of cancer immunotherapies, which aim to enhance the body's natural immune response against cancer. These therapies include checkpoint inhibitors, which block proteins that inhibit T cell activation, and therapeutic vaccines, which stimulate an immune response against specific tumor antigens.

Surface antigens are molecules found on the surface of cells that can be recognized by the immune system as being foreign or different from the host's own cells. Antigens are typically proteins or polysaccharides that are capable of stimulating an immune response, leading to the production of antibodies and activation of immune cells such as T-cells.

Surface antigens are important in the context of infectious diseases because they allow the immune system to identify and target infected cells for destruction. For example, viruses and bacteria often display surface antigens that are distinct from those found on host cells, allowing the immune system to recognize and attack them. In some cases, these surface antigens can also be used as targets for vaccines or other immunotherapies.

In addition to their role in infectious diseases, surface antigens are also important in the context of cancer. Tumor cells often display abnormal surface antigens that differ from those found on normal cells, allowing the immune system to potentially recognize and attack them. However, tumors can also develop mechanisms to evade the immune system, making it difficult to mount an effective response.

Overall, understanding the properties and behavior of surface antigens is crucial for developing effective immunotherapies and vaccines against infectious diseases and cancer.

Antibodies are proteins produced by the immune system in response to the presence of a foreign substance, known as an antigen. They are capable of recognizing and binding to specific antigens, neutralizing or marking them for destruction by other immune cells.

Helminths are parasitic worms that can infect humans and animals. They include roundworms, tapeworms, and flukes, among others. Helminth infections can cause a range of symptoms, depending on the type of worm and the location of the infection.

Antibodies to helminths are produced by the immune system in response to an infection with one of these parasitic worms. These antibodies can be detected in the blood and serve as evidence of a current or past infection. They may also play a role in protecting against future infections with the same type of worm.

There are several different classes of antibodies, including IgA, IgD, IgE, IgG, and IgM. Antibodies to helminths are typically of the IgE class, which are associated with allergic reactions and the defense against parasites. IgE antibodies can bind to mast cells and basophils, triggering the release of histamine and other inflammatory mediators that help to protect against the worm.

In addition to IgE, other classes of antibodies may also be produced in response to a helminth infection. For example, IgG antibodies may be produced later in the course of the infection and can provide long-term immunity to reinfection. IgA antibodies may also be produced and can help to prevent the attachment and entry of the worm into the body.

Overall, the production of antibodies to helminths is an important part of the immune response to these parasitic worms. However, in some cases, the presence of these antibodies may also be associated with allergic reactions or other immunological disorders.

An antigen is any substance that can stimulate an immune response, particularly the production of antibodies. Viral antigens are antigens that are found on or produced by viruses. They can be proteins, glycoproteins, or carbohydrates present on the surface or inside the viral particle.

Viral antigens play a crucial role in the immune system's recognition and response to viral infections. When a virus infects a host cell, it may display its antigens on the surface of the infected cell. This allows the immune system to recognize and target the infected cells for destruction, thereby limiting the spread of the virus.

Viral antigens are also important targets for vaccines. Vaccines typically work by introducing a harmless form of a viral antigen to the body, which then stimulates the production of antibodies and memory T-cells that can recognize and respond quickly and effectively to future infections with the actual virus.

It's worth noting that different types of viruses have different antigens, and these antigens can vary between strains of the same virus. This is why there are often different vaccines available for different viral diseases, and why flu vaccines need to be updated every year to account for changes in the circulating influenza virus strains.

"Trichuris" is a genus of parasitic roundworms that are known to infect the intestines of various mammals, including humans. The species that commonly infects humans is called "Trichuris trichiura," which is also known as the human whipworm. These worms are named for their long, thin shape that resembles a whip.

The life cycle of Trichuris involves ingestion of eggs containing infective larvae through contaminated food or water. Once inside the human body, the larvae hatch and migrate to the large intestine, where they mature into adult worms that live in the caecum and colon. Adult female worms lay thousands of eggs every day, which are passed in the feces and can survive in the environment for years, waiting to infect a new host.

Infections with Trichuris trichiura can cause symptoms such as diarrhea, abdominal pain, bloating, and weight loss. In severe cases, it can lead to anemia, malnutrition, and impaired growth in children. Treatment for trichuriasis typically involves medication that kills the adult worms, such as albendazole or mebendazole.

Ancylostomatoidea is a superfamily of nematode (roundworm) parasites that includes the genera Ancylostoma and Necator, which are commonly known as hookworms. These parasites are primarily found in the small intestine of their hosts, which can include humans and other animals.

Ancylostomatoidea parasites have a complex life cycle that involves both free-living and parasitic stages. The life cycle begins when the parasite's eggs are passed in the feces of an infected host and hatch into larvae in the soil. The larvae then infect a new host by penetrating the skin, usually through contact with contaminated soil.

Once inside the host, the larvae migrate through the body to the lungs, where they mature and are coughed up and swallowed, allowing them to reach the small intestine. Here, they attach to the intestinal wall and feed on the host's blood, causing anemia and other symptoms of hookworm infection.

Hookworm infections can cause a range of symptoms, including abdominal pain, diarrhea, weight loss, and fatigue. In severe cases, they can lead to anemia, intestinal obstruction, and even death. Prevention measures include wearing shoes in areas with contaminated soil, practicing good hygiene, and treating infected individuals to prevent the spread of the parasite.

Anthelmintics are a type of medication used to treat infections caused by parasitic worms, also known as helminths. These medications work by either stunting the growth of the worms, paralyzing them, or killing them outright, allowing the body to expel the worms through normal bodily functions. Anthelmintics are commonly used to treat infections caused by roundworms, tapeworms, flukeworms, and hookworms. Examples of anthelmintic drugs include albendazole, mebendazole, praziquantel, and ivermectin.

Helminth proteins refer to the proteins that are produced and expressed by helminths, which are parasitic worms that cause diseases in humans and animals. These proteins can be found on the surface or inside the helminths and play various roles in their biology, such as in development, reproduction, and immune evasion. Some helminth proteins have been identified as potential targets for vaccines or drug development, as blocking their function may help to control or eliminate helminth infections. Examples of helminth proteins that have been studied include the antigen Bm86 from the cattle tick Boophilus microplus, and the tetraspanin protein Sm22.6 from the blood fluke Schistosoma mansoni.

Antigens are substances (usually proteins) found on the surface of cells, or viruses, that can be recognized by the immune system and stimulate an immune response. In the context of protozoa, antigens refer to the specific proteins or other molecules found on the surface of these single-celled organisms that can trigger an immune response in a host organism.

Protozoa are a group of microscopic eukaryotic organisms that include a diverse range of species, some of which can cause diseases in humans and animals. When a protozoan infects a host, the host's immune system recognizes the protozoan antigens as foreign and mounts an immune response to eliminate the infection. This response involves the activation of various types of immune cells, such as T-cells and B-cells, which recognize and target the protozoan antigens.

Understanding the nature of protozoan antigens is important for developing vaccines and other immunotherapies to prevent or treat protozoan infections. For example, researchers have identified specific antigens on the surface of the malaria parasite that are recognized by the human immune system and have used this information to develop vaccine candidates. However, many protozoan infections remain difficult to prevent or treat, and further research is needed to identify new targets for vaccines and therapies.

Nematospiroides dubius is a type of parasitic roundworm that primarily infects rodents, particularly mice. The adult worms reside in the small intestine and reproduce by releasing eggs into the host's feces. These eggs can then be ingested by other hosts, continuing the life cycle of the parasite.

While Nematospiroides dubius is not commonly known to infect humans, there have been rare cases of human infection reported in the literature. In such cases, the parasite is not believed to cause significant disease or symptoms in healthy individuals. However, it may be a potential confounding factor in research studies investigating allergic responses and intestinal inflammation.

It's worth noting that Nematospiroides dubius has been used as a laboratory model for studying immunity to helminth infections, particularly in the context of Th2-mediated immune responses.

Strongylida infections are a group of parasitic diseases caused by roundworms that belong to the order Strongylida. These nematodes infect various hosts, including humans, causing different clinical manifestations depending on the specific species involved. Here are some examples:

1. Strongyloidiasis: This is an infection caused by the nematode Strongyloides stercoralis. The parasite can penetrate the skin and migrate to the lungs and small intestine, causing respiratory and gastrointestinal symptoms such as cough, wheezing, abdominal pain, and diarrhea. In immunocompromised individuals, the infection can become severe and disseminated, leading to systemic illness and even death.
2. Hookworm infections: The hookworms Ancylostoma duodenale and Necator americanus infect humans through skin contact with contaminated soil. The larvae migrate to the lungs and then to the small intestine, where they attach to the intestinal wall and feed on blood. Heavy infections can cause anemia, protein loss, and developmental delays in children.
3. Trichostrongyliasis: This is a group of infections caused by various species of nematodes that infect the gastrointestinal tract of humans and animals. The parasites can cause symptoms such as abdominal pain, diarrhea, and anemia.
4. Toxocariasis: This is an infection caused by the roundworms Toxocara canis or Toxocara cati, which infect dogs and cats, respectively. Humans can become infected through accidental ingestion of contaminated soil or food. The larvae migrate to various organs such as the liver, lungs, and eyes, causing symptoms such as fever, cough, abdominal pain, and vision loss.

Preventive measures for Strongylida infections include personal hygiene, proper sanitation, and avoidance of contact with contaminated soil or water. Treatment usually involves antiparasitic drugs such as albendazole or ivermectin, depending on the specific infection and severity of symptoms.

Polyomavirus transforming antigens refer to specific proteins expressed by polyomaviruses that can induce cellular transformation and lead to the development of cancer. These antigens are called large T antigen (T-Ag) and small t antigen (t-Ag). They manipulate key cellular processes, such as cell cycle regulation and DNA damage response, leading to uncontrolled cell growth and malignant transformation.

The large T antigen is a multifunctional protein that plays a crucial role in viral replication and transformation. It has several domains with different functions:

1. Origin binding domain (OBD): Binds to the viral origin of replication, initiating DNA synthesis.
2. Helicase domain: Unwinds double-stranded DNA during replication.
3. DNA binding domain: Binds to specific DNA sequences and acts as a transcriptional regulator.
4. Protein phosphatase 1 (PP1) binding domain: Recruits PP1 to promote viral DNA replication and inhibit host cell defense mechanisms.
5. p53-binding domain: Binds and inactivates the tumor suppressor protein p53, promoting cell cycle progression and preventing apoptosis.
6. Rb-binding domain: Binds to and inactivates the retinoblastoma protein (pRb), leading to deregulation of the cell cycle and uncontrolled cell growth.

The small t antigen shares a common N-terminal region with large T antigen but lacks some functional domains, such as the OBD and helicase domain. Small t antigen can also bind to and inactivate PP1 and pRb, contributing to transformation. However, its primary role is to stabilize large T antigen by preventing its proteasomal degradation.

Polyomavirus transforming antigens are associated with various human cancers, such as Merkel cell carcinoma (caused by Merkel cell polyomavirus) and some forms of brain tumors, sarcomas, and lymphomas (associated with simian virus 40).

HLA (Human Leukocyte Antigen) antigens are a group of proteins found on the surface of cells in our body. They play a crucial role in the immune system's ability to differentiate between "self" and "non-self." HLA antigens are encoded by a group of genes located on chromosome 6, known as the major histocompatibility complex (MHC).

There are three types of HLA antigens: HLA class I, HLA class II, and HLA class III. HLA class I antigens are found on the surface of almost all cells in the body and help the immune system recognize and destroy virus-infected or cancerous cells. They consist of three components: HLA-A, HLA-B, and HLA-C.

HLA class II antigens are primarily found on the surface of immune cells, such as macrophages, B cells, and dendritic cells. They assist in the presentation of foreign particles (like bacteria and viruses) to CD4+ T cells, which then activate other parts of the immune system. HLA class II antigens include HLA-DP, HLA-DQ, and HLA-DR.

HLA class III antigens consist of various molecules involved in immune responses, such as cytokines and complement components. They are not directly related to antigen presentation.

The genetic diversity of HLA antigens is extensive, with thousands of variations or alleles. This diversity allows for a better ability to recognize and respond to a wide range of pathogens. However, this variation can also lead to compatibility issues in organ transplantation, as the recipient's immune system may recognize the donor's HLA antigens as foreign and attack the transplanted organ.

Nematode infections, also known as roundworm infections, are caused by various species of nematodes or roundworms. These parasitic worms can infect humans and animals, leading to a range of health problems depending on the specific type of nematode and the location of the infection within the body.

Common forms of nematode infections include:

1. Ascariasis: Caused by Ascaris lumbricoides, this infection occurs when people ingest the parasite's eggs through contaminated food or water. The larvae hatch in the small intestine, mature into adult worms, and can cause abdominal pain, nausea, vomiting, and diarrhea. In severe cases, the worms may obstruct the intestines or migrate to other organs, leading to potentially life-threatening complications.
2. Hookworm infections: These are caused by Ancylostoma duodenale and Necator americanus. The larvae penetrate the skin, usually through bare feet, and migrate to the small intestine, where they attach to the intestinal wall and feed on blood. Symptoms include abdominal pain, diarrhea, anemia, and protein loss.
3. Trichuriasis: Also known as whipworm infection, this is caused by Trichuris trichiura. The larvae hatch in the small intestine, mature into adult worms, and reside in the large intestine, causing abdominal pain, diarrhea, and rectal prolapse in severe cases.
4. Strongyloidiasis: Caused by Strongyloides stercoralis, this infection occurs when the larvae penetrate the skin, usually through contaminated soil, and migrate to the lungs and then the small intestine. Symptoms include abdominal pain, diarrhea, and skin rashes. In immunocompromised individuals, strongyloidiasis can lead to disseminated disease, which is potentially fatal.
5. Toxocariasis: This infection is caused by the roundworms Toxocara canis or Toxocara cati, found in dogs and cats, respectively. Humans become infected through ingestion of contaminated soil or undercooked meat. Symptoms include fever, cough, abdominal pain, and vision loss in severe cases.
6. Enterobiasis: Also known as pinworm infection, this is caused by Enterobius vermicularis. The larvae hatch in the small intestine, mature into adult worms, and reside in the large intestine, causing perianal itching and restlessness, especially at night.

Preventive measures include:

1. Proper hand hygiene: Wash hands with soap and water after using the toilet, changing diapers, handling pets or their feces, and before preparing or eating food.
2. Personal hygiene: Keep fingernails short and clean, avoid biting nails, and wear shoes in public areas, especially where soil may be contaminated with human or animal feces.
3. Food safety: Wash fruits and vegetables thoroughly, cook meat properly, and avoid consuming raw or undercooked meat, poultry, or fish.
4. Environmental cleanliness: Regularly clean surfaces that come into contact with food, such as countertops, cutting boards, and utensils. Dispose of trash properly and maintain a clean living environment.
5. Pet care: Keep pets healthy and regularly deworm them as recommended by a veterinarian. Pick up pet feces promptly to prevent contamination of the environment.
6. Public health measures: Implement public health interventions, such as regular waste disposal, sewage treatment, and vector control, to reduce the transmission of parasitic infections.

Cestoda is a class of parasitic worms belonging to the phylum Platyhelminthes, also known as flatworms. Cestodes are commonly known as tapeworms and have a long, flat, segmented body that can grow to considerable length in their adult form. They lack a digestive system and absorb nutrients through their body surface.

Cestodes have a complex life cycle involving one or two intermediate hosts, usually insects or crustaceans, and a definitive host, which is typically a mammal, including humans. The tapeworm's larval stage develops in the intermediate host, and when the definitive host consumes the infected intermediate host, the larvae mature into adults in the host's intestine.

Humans can become infected with tapeworms by eating raw or undercooked meat from infected animals or through accidental ingestion of contaminated water or food containing tapeworm eggs or larvae. Infection with tapeworms can cause various symptoms, including abdominal pain, diarrhea, weight loss, and vitamin deficiencies.

Fungal antigens are substances found on or produced by fungi that can stimulate an immune response in a host organism. They can be proteins, polysaccharides, or other molecules that are recognized as foreign by the host's immune system. Fungal antigens can be used in diagnostic tests to identify fungal infections, and they can also be targets of immune responses during fungal infections. In some cases, fungal antigens may contribute to the pathogenesis of fungal diseases by inducing inflammatory or allergic reactions. Examples of fungal antigens include the cell wall components of Candida albicans and the extracellular polysaccharide galactomannan produced by Aspergillus fumigatus.

CD (cluster of differentiation) antigens are cell-surface proteins that are expressed on leukocytes (white blood cells) and can be used to identify and distinguish different subsets of these cells. They are important markers in the field of immunology and hematology, and are commonly used to diagnose and monitor various diseases, including cancer, autoimmune disorders, and infectious diseases.

CD antigens are designated by numbers, such as CD4, CD8, CD19, etc., which refer to specific proteins found on the surface of different types of leukocytes. For example, CD4 is a protein found on the surface of helper T cells, while CD8 is found on cytotoxic T cells.

CD antigens can be used as targets for immunotherapy, such as monoclonal antibody therapy, in which antibodies are designed to bind to specific CD antigens and trigger an immune response against cancer cells or infected cells. They can also be used as markers to monitor the effectiveness of treatments and to detect minimal residual disease (MRD) after treatment.

It's important to note that not all CD antigens are exclusive to leukocytes, some can be found on other cell types as well, and their expression can vary depending on the activation state or differentiation stage of the cells.

A "Parasite Egg Count" is a laboratory measurement used to estimate the number of parasitic eggs present in a fecal sample. It is commonly used in veterinary and human medicine to diagnose and monitor parasitic infections, such as those caused by roundworms, hookworms, tapeworms, and other intestinal helminths (parasitic worms).

The most common method for measuring parasite egg counts is the McMaster technique. This involves mixing a known volume of feces with a flotation solution, which causes the eggs to float to the top of the mixture. A small sample of this mixture is then placed on a special counting chamber and examined under a microscope. The number of eggs present in the sample is then multiplied by a dilution factor to estimate the total number of eggs per gram (EPG) of feces.

Parasite egg counts can provide valuable information about the severity of an infection, as well as the effectiveness of treatment. However, it is important to note that not all parasitic infections produce visible eggs in the feces, and some parasites may only shed eggs intermittently. Therefore, a negative egg count does not always rule out the presence of a parasitic infection.

H-2 antigens are a group of cell surface proteins found in mice that play a critical role in the immune system. They are similar to the human leukocyte antigen (HLA) complex in humans and are involved in the presentation of peptide antigens to T cells, which is a crucial step in the adaptive immune response.

The H-2 antigens are encoded by a cluster of genes located on chromosome 17 in mice. They are highly polymorphic, meaning that there are many different variations of these proteins circulating in the population. This genetic diversity allows for a wide range of potential peptide antigens to be presented to T cells, thereby enhancing the ability of the immune system to recognize and respond to a variety of pathogens.

The H-2 antigens are divided into two classes based on their function and structure. Class I H-2 antigens are found on almost all nucleated cells and consist of a heavy chain, a light chain, and a peptide fragment. They present endogenous peptides, such as those derived from viruses that infect the cell, to CD8+ T cells.

Class II H-2 antigens, on the other hand, are found primarily on professional antigen-presenting cells, such as dendritic cells and macrophages. They consist of an alpha chain and a beta chain and present exogenous peptides, such as those derived from bacteria that have been engulfed by the cell, to CD4+ T cells.

Overall, H-2 antigens are essential components of the mouse immune system, allowing for the recognition and elimination of pathogens and infected cells.

Albendazole is an antiparasitic medication used to treat a variety of parasitic infections, including neurocysticercosis (a tapeworm infection that affects the brain), hydatid disease (a parasitic infection that can affect various organs), and other types of worm infestations such as pinworm, roundworm, hookworm, and whipworm infections.

Albendazole works by inhibiting the polymerization of beta-tubulin, a protein found in the microtubules of parasitic cells, which disrupts the parasite's ability to maintain its shape and move. This leads to the death of the parasite and elimination of the infection.

Albendazole is available in oral form and is typically taken two to three times a day with meals for several days or weeks, depending on the type and severity of the infection being treated. Common side effects of albendazole include nausea, vomiting, diarrhea, abdominal pain, and headache. Rare but serious side effects may include liver damage, bone marrow suppression, and neurological problems.

It is important to note that albendazole should only be used under the supervision of a healthcare provider, as it can have serious side effects and interactions with other medications. Additionally, it is not effective against all types of parasitic infections, so proper diagnosis is essential before starting treatment.

Carcinoembryonic antigen (CEA) is a protein that is normally produced in small amounts during fetal development. In adults, low levels of CEA can be found in the blood, but elevated levels are typically associated with various types of cancer, particularly colon, rectal, and breast cancer.

Measurement of CEA levels in the blood is sometimes used as a tumor marker to monitor response to treatment, detect recurrence, or screen for secondary cancers in patients with a history of certain types of cancer. However, it's important to note that CEA is not a specific or sensitive indicator of cancer and can be elevated in various benign conditions such as inflammation, smoking, and some gastrointestinal diseases. Therefore, the test should be interpreted in conjunction with other clinical and diagnostic findings.

Antigens are substances that trigger an immune response in the body, leading to the production of antibodies. Antigens can be proteins, polysaccharides, or other molecules found on the surface of cells or viruses.

Viral antigens are antigens that are present on the surface of viruses. When a virus infects a cell, it may display viral antigens on the surface of the infected cell. This can alert the immune system to the presence of the virus and trigger an immune response.

Tumor antigens are antigens that are present on the surface of cancer cells. These antigens may be unique to the cancer cells, or they may be similar to antigens found on normal cells. Tumor antigens can be recognized by the immune system as foreign, leading to an immune response against the cancer cells.

It is important to note that not all viral infections lead to cancer, and not all tumors are caused by viruses. However, some viruses have been linked to an increased risk of certain types of cancer. For example, human papillomavirus (HPV) has been associated with an increased risk of cervical, anal, and oral cancers. In these cases, the virus may introduce viral antigens into the cells it infects, leading to an altered presentation of tumor antigens on the surface of the infected cells. This can potentially trigger an immune response against both the viral antigens and the tumor antigens, which may help to prevent or slow the growth of the cancer.

"Schistosoma mansoni" is a specific species of parasitic flatworm, also known as a blood fluke, that causes the disease schistosomiasis (also known as snail fever). This trematode has a complex life cycle involving both freshwater snails and humans. The adult worms live in the blood vessels of the human host, particularly in the venous plexus of the intestines, where they lay eggs that are excreted through feces. These eggs can hatch in fresh water and infect specific snail species, which then release a free-swimming form called cercariae. These cercariae can penetrate the skin of humans who come into contact with infested water, leading to infection and subsequent health complications if left untreated.

The medical definition of "Schistosoma mansoni" is: A species of trematode parasitic flatworm that causes schistosomiasis in humans through its complex life cycle involving freshwater snails as an intermediate host. Adult worms reside in the blood vessels of the human host, particularly those surrounding the intestines, and release eggs that are excreted through feces. Infection occurs when cercariae, released by infected snails, penetrate human skin during contact with infested water.

Filarioidea is a superfamily of parasitic nematode (roundworm) worms, many of which are important pathogens in humans and animals. They are transmitted to their hosts through the bite of insect vectors, such as mosquitoes or flies. The filarioid worms can cause a range of diseases known as filariases. Some examples include Wuchereria bancrofti, Brugia malayi, and Onchocerca volvulus, which cause lymphatic filariasis (elephantiasis) and river blindness, respectively. The adult worms live in the lymphatic system or subcutaneous tissues of their hosts, where they produce microfilariae, the infective stage for the insect vector.

The medical definition of Filarioidea is: A superfamily of parasitic nematode worms that includes several important human pathogens and causes various filariases. The adult worms live in the lymphatic system or subcutaneous tissues, while the microfilariae are taken up by insect vectors during a blood meal and develop into infective larvae inside the vector. These larvae are then transmitted to a new host through the bite of the infected vector.

HLA-DR antigens are a type of human leukocyte antigen (HLA) class II molecule that plays a crucial role in the immune system. They are found on the surface of antigen-presenting cells, such as dendritic cells, macrophages, and B lymphocytes. HLA-DR molecules present peptide antigens to CD4+ T cells, also known as helper T cells, thereby initiating an immune response.

HLA-DR antigens are highly polymorphic, meaning that there are many different variants of these molecules in the human population. This diversity allows for a wide range of potential peptide antigens to be presented and recognized by the immune system. HLA-DR antigens are encoded by genes located on chromosome 6 in the major histocompatibility complex (MHC) region.

In transplantation, HLA-DR compatibility between donor and recipient is an important factor in determining the success of the transplant. Incompatibility can lead to a heightened immune response against the transplanted organ or tissue, resulting in rejection. Additionally, certain HLA-DR types have been associated with increased susceptibility to autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis.

1. Receptors: In the context of physiology and medicine, receptors are specialized proteins found on the surface of cells or inside cells that detect and respond to specific molecules, known as ligands. These interactions can trigger a range of responses within the cell, such as starting a signaling pathway or changing the cell's behavior. There are various types of receptors, including ion channels, G protein-coupled receptors, and enzyme-linked receptors.

2. Antigen: An antigen is any substance (usually a protein) that can be recognized by the immune system, specifically by antibodies or T-cells, as foreign and potentially harmful. Antigens can be derived from various sources, such as bacteria, viruses, fungi, parasites, or even non-living substances like pollen, chemicals, or toxins. An antigen typically contains epitopes, which are the specific regions that antibodies or T-cell receptors recognize and bind to.

3. T-Cell: Also known as T lymphocytes, T-cells are a type of white blood cell that plays a crucial role in cell-mediated immunity, a part of the adaptive immune system. They are produced in the bone marrow and mature in the thymus gland. There are several types of T-cells, including CD4+ helper T-cells, CD8+ cytotoxic T-cells, and regulatory T-cells (Tregs). T-cells recognize antigens presented to them by antigen-presenting cells (APCs) via their surface receptors called the T-cell receptor (TCR). Once activated, T-cells can proliferate and differentiate into various effector cells that help eliminate infected or damaged cells.

Schistosoma is a genus of flatworms that cause the disease schistosomiasis, also known as snail fever. These parasitic worms infect freshwater snails and then release a form of the parasite that can penetrate the skin of humans when they come into contact with contaminated water. The larvae mature into adult worms in the human body, living in the blood vessels of the bladder, intestines or other organs, where they lay eggs. These eggs can cause serious damage to internal organs and lead to a range of symptoms including fever, chills, diarrhea, and anemia. Schistosomiasis is a significant public health problem in many tropical and subtropical regions around the world.

Protozoan infections are diseases caused by microscopic, single-celled organisms known as protozoa. These parasites can enter the human body through contaminated food, water, or contact with an infected person or animal. Once inside the body, they can multiply and cause a range of symptoms depending on the type of protozoan and where it infects in the body. Some common protozoan infections include malaria, giardiasis, amoebiasis, and toxoplasmosis. Symptoms can vary widely but may include diarrhea, abdominal pain, fever, fatigue, and skin rashes. Treatment typically involves the use of antiprotozoal medications to kill the parasites and alleviate symptoms.

Monoclonal antibodies are a type of antibody that are identical because they are produced by a single clone of cells. They are laboratory-produced molecules that act like human antibodies in the immune system. They can be designed to attach to specific proteins found on the surface of cancer cells, making them useful for targeting and treating cancer. Monoclonal antibodies can also be used as a therapy for other diseases, such as autoimmune disorders and inflammatory conditions.

Monoclonal antibodies are produced by fusing a single type of immune cell, called a B cell, with a tumor cell to create a hybrid cell, or hybridoma. This hybrid cell is then able to replicate indefinitely, producing a large number of identical copies of the original antibody. These antibodies can be further modified and engineered to enhance their ability to bind to specific targets, increase their stability, and improve their effectiveness as therapeutic agents.

Monoclonal antibodies have several mechanisms of action in cancer therapy. They can directly kill cancer cells by binding to them and triggering an immune response. They can also block the signals that promote cancer growth and survival. Additionally, monoclonal antibodies can be used to deliver drugs or radiation directly to cancer cells, increasing the effectiveness of these treatments while minimizing their side effects on healthy tissues.

Monoclonal antibodies have become an important tool in modern medicine, with several approved for use in cancer therapy and other diseases. They are continuing to be studied and developed as a promising approach to treating a wide range of medical conditions.

BALB/c is an inbred strain of laboratory mouse that is widely used in biomedical research. The strain was developed at the Institute of Cancer Research in London by Henry Baldwin and his colleagues in the 1920s, and it has since become one of the most commonly used inbred strains in the world.

BALB/c mice are characterized by their black coat color, which is determined by a recessive allele at the tyrosinase locus. They are also known for their docile and friendly temperament, making them easy to handle and work with in the laboratory.

One of the key features of BALB/c mice that makes them useful for research is their susceptibility to certain types of tumors and immune responses. For example, they are highly susceptible to developing mammary tumors, which can be induced by chemical carcinogens or viral infection. They also have a strong Th2-biased immune response, which makes them useful models for studying allergic diseases and asthma.

BALB/c mice are also commonly used in studies of genetics, neuroscience, behavior, and infectious diseases. Because they are an inbred strain, they have a uniform genetic background, which makes it easier to control for genetic factors in experiments. Additionally, because they have been bred in the laboratory for many generations, they are highly standardized and reproducible, making them ideal subjects for scientific research.

Histocompatibility antigens, also known as human leukocyte antigens (HLAs), are proteins found on the surface of most cells in the body. They play a critical role in the immune system's ability to differentiate between "self" and "non-self" cells. Histocompatibility antigens are encoded by a group of genes called the major histocompatibility complex (MHC).

There are two main types of histocompatibility antigens: class I and class II. Class I antigens are found on almost all nucleated cells, while class II antigens are primarily expressed on immune cells such as B cells, macrophages, and dendritic cells. These antigens present pieces of proteins (peptides) from both inside and outside the cell to T-cells, a type of white blood cell that plays a central role in the immune response.

When foreign peptides are presented to T-cells by histocompatibility antigens, it triggers an immune response aimed at eliminating the threat. This is why histocompatibility antigens are so important in organ transplantation - if the donor's and recipient's antigens do not match closely enough, the recipient's immune system may recognize the transplanted organ as foreign and attack it.

Understanding the role of histocompatibility antigens has been crucial in developing techniques for matching donors and recipients in organ transplantation, as well as in diagnosing and treating various autoimmune diseases and cancers.

Schistosomiasis mansoni is a parasitic infection caused by the trematode flatworm Schistosoma mansoni. The disease cycle begins when human hosts come into contact with fresh water contaminated with the parasite's larvae, called cercariae, which are released from infected snail intermediate hosts.

Once the cercariae penetrate the skin of a human host, they transform into schistosomula and migrate through various tissues before reaching the hepatic portal system. Here, the parasites mature into adult worms, mate, and produce eggs that can cause inflammation and damage to the intestinal wall, liver, spleen, and other organs.

Symptoms of schistosomiasis mansoni may include fever, chills, cough, diarrhea, abdominal pain, and blood in stool or urine. Chronic infection can lead to severe complications such as fibrosis of the liver, kidney damage, bladder cancer, and neurological disorders.

Preventive measures include avoiding contact with contaminated water sources, proper sanitation, and access to safe drinking water. Treatment typically involves administering a single dose of the drug praziquantel, which is effective in eliminating the adult worms and reducing egg production. However, it does not prevent reinfection.

Proliferating Cell Nuclear Antigen (PCNA) is a protein that plays an essential role in the process of DNA replication and repair in eukaryotic cells. It functions as a cofactor for DNA polymerase delta, enhancing its activity during DNA synthesis. PCNA forms a sliding clamp around DNA, allowing it to move along the template and coordinate the actions of various enzymes involved in DNA metabolism.

PCNA is often used as a marker for cell proliferation because its levels increase in cells that are actively dividing or have been stimulated to enter the cell cycle. Immunostaining techniques can be used to detect PCNA and determine the proliferative status of tissues or cultures. In this context, 'proliferating' refers to the rapid multiplication of cells through cell division.

Schistosomiasis, also known as bilharzia or snail fever, is a parasitic infection caused by several species of the trematode flatworm Schistosoma. The infection occurs when people come into contact with freshwater contaminated with the parasite's larvae, which are released by infected freshwater snails.

The larvae penetrate the skin, enter the bloodstream, and mature into adult worms in the blood vessels of the urinary tract or intestines. The female worms lay eggs, which can cause inflammation and scarring in various organs, including the liver, lungs, and brain.

Symptoms of schistosomiasis may include fever, chills, cough, muscle aches, and diarrhea. In chronic cases, the infection can lead to serious complications such as kidney damage, bladder cancer, and seizures. Schistosomiasis is prevalent in tropical and subtropical regions with poor sanitation and lack of access to safe drinking water. It is preventable through improved water supply, sanitation, and snail control measures. Treatment typically involves the use of a medication called praziquantel, which kills the adult worms.

Cestode infections, also known as tapeworm infections, are caused by the ingestion of larval cestodes (tapeworms) present in undercooked meat or contaminated water. The most common types of cestode infections in humans include:

1. Taeniasis: This is an infection with the adult tapeworm of the genus Taenia, such as Taenia saginata (beef tapeworm) and Taenia solium (pork tapeworm). Humans become infected by consuming undercooked beef or pork that contains viable tapeworm larvae. The larvae then mature into adult tapeworms in the human intestine, where they can live for several years, producing eggs that are passed in the feces.
2. Hydatid disease: This is a zoonotic infection caused by the larval stage of the tapeworm Echinococcus granulosus, which is commonly found in dogs and other carnivores. Humans become infected by accidentally ingesting eggs present in dog feces or contaminated food or water. The eggs hatch in the human intestine and release larvae that migrate to various organs, such as the liver or lungs, where they form hydatid cysts. These cysts can grow slowly over several years and cause symptoms depending on their location and size.
3. Diphyllobothriasis: This is an infection with the fish tapeworm Diphyllobothrium latum, which is found in freshwater fish. Humans become infected by consuming raw or undercooked fish that contain viable tapeworm larvae. The larvae mature into adult tapeworms in the human intestine and can cause symptoms such as abdominal pain, diarrhea, and vitamin B12 deficiency.

Preventing cestode infections involves practicing good hygiene, cooking meat thoroughly, avoiding consumption of raw or undercooked fish, and washing fruits and vegetables carefully before eating. In some cases, treatment with antiparasitic drugs may be necessary to eliminate the tapeworms from the body.

An epitope is a specific region on the surface of an antigen (a molecule that can trigger an immune response) that is recognized by an antibody, B-cell receptor, or T-cell receptor. It is also commonly referred to as an antigenic determinant. Epitopes are typically composed of linear amino acid sequences or conformational structures made up of discontinuous amino acids in the antigen. They play a crucial role in the immune system's ability to differentiate between self and non-self molecules, leading to the targeted destruction of foreign substances like viruses and bacteria. Understanding epitopes is essential for developing vaccines, diagnostic tests, and immunotherapies.

CD15 is a type of antigen that is found on the surface of certain types of white blood cells called neutrophils and monocytes. It is also expressed on some types of cancer cells, including myeloid leukemia cells and some lymphomas. CD15 antigens are part of a group of molecules known as carbohydrate antigens because they contain sugar-like substances called carbohydrates.

CD15 antigens play a role in the immune system's response to infection and disease. They can be recognized by certain types of immune cells, such as natural killer (NK) cells and cytotoxic T cells, which can then target and destroy cells that express CD15 antigens. In cancer, the presence of CD15 antigens on the surface of cancer cells can make them more visible to the immune system, potentially triggering an immune response against the cancer.

CD15 antigens are also used as a marker in laboratory tests to help identify and classify different types of white blood cells and cancer cells. For example, CD15 staining is often used in the diagnosis of acute myeloid leukemia (AML) to distinguish it from other types of leukemia.

Histocompatibility antigens Class II are a group of cell surface proteins that play a crucial role in the immune system's response to foreign substances. They are expressed on the surface of various cells, including immune cells such as B lymphocytes, macrophages, dendritic cells, and activated T lymphocytes.

Class II histocompatibility antigens are encoded by the major histocompatibility complex (MHC) class II genes, which are located on chromosome 6 in humans. These antigens are composed of two non-covalently associated polypeptide chains, an alpha (α) and a beta (β) chain, which form a heterodimer. There are three main types of Class II histocompatibility antigens, known as HLA-DP, HLA-DQ, and HLA-DR.

Class II histocompatibility antigens present peptide antigens to CD4+ T helper cells, which then activate other immune cells, such as B cells and macrophages, to mount an immune response against the presented antigen. Because of their role in initiating an immune response, Class II histocompatibility antigens are important in transplantation medicine, where mismatches between donor and recipient can lead to rejection of the transplanted organ or tissue.

Feces are the solid or semisolid remains of food that could not be digested or absorbed in the small intestine, along with bacteria and other waste products. After being stored in the colon, feces are eliminated from the body through the rectum and anus during defecation. Feces can vary in color, consistency, and odor depending on a person's diet, health status, and other factors.

Immunoglobulin G (IgG) is a type of antibody, which is a protective protein produced by the immune system in response to foreign substances like bacteria or viruses. IgG is the most abundant type of antibody in human blood, making up about 75-80% of all antibodies. It is found in all body fluids and plays a crucial role in fighting infections caused by bacteria, viruses, and toxins.

IgG has several important functions:

1. Neutralization: IgG can bind to the surface of bacteria or viruses, preventing them from attaching to and infecting human cells.
2. Opsonization: IgG coats the surface of pathogens, making them more recognizable and easier for immune cells like neutrophils and macrophages to phagocytose (engulf and destroy) them.
3. Complement activation: IgG can activate the complement system, a group of proteins that work together to help eliminate pathogens from the body. Activation of the complement system leads to the formation of the membrane attack complex, which creates holes in the cell membranes of bacteria, leading to their lysis (destruction).
4. Antibody-dependent cellular cytotoxicity (ADCC): IgG can bind to immune cells like natural killer (NK) cells and trigger them to release substances that cause target cells (such as virus-infected or cancerous cells) to undergo apoptosis (programmed cell death).
5. Immune complex formation: IgG can form immune complexes with antigens, which can then be removed from the body through various mechanisms, such as phagocytosis by immune cells or excretion in urine.

IgG is a critical component of adaptive immunity and provides long-lasting protection against reinfection with many pathogens. It has four subclasses (IgG1, IgG2, IgG3, and IgG4) that differ in their structure, function, and distribution in the body.

Prostate-Specific Antigen (PSA) is a glycoprotein enzyme produced by the epithelial cells of the prostate gland. It is primarily involved in liquefying semen after ejaculation, allowing sperm mobility.

In clinical medicine, PSA is used as a tumor marker, mainly for monitoring the treatment and recurrence of prostate cancer. Elevated levels of PSA can indicate inflammation, infection, benign prostatic hyperplasia (BPH), or prostate cancer. However, it's important to note that an elevated PSA level does not necessarily confirm cancer; further diagnostic tests like digital rectal examination, transrectal ultrasound, and prostate biopsy are often required for definitive diagnosis.

Doctors may also use PSA isoforms or derivatives, such as free PSA, total PSA, and PSA density, to help improve the specificity of cancer detection and differentiate between malignant and benign conditions.

"O antigens" are a type of antigen found on the lipopolysaccharide (LPS) component of the outer membrane of Gram-negative bacteria. The "O" in O antigens stands for "outer" membrane. These antigens are composed of complex carbohydrates and can vary between different strains of the same species of bacteria, which is why they are also referred to as the bacterial "O" somatic antigens.

The O antigens play a crucial role in the virulence and pathogenesis of many Gram-negative bacteria, as they help the bacteria evade the host's immune system by changing the structure of the O antigen, making it difficult for the host to mount an effective immune response against the bacterial infection.

The identification and classification of O antigens are important in epidemiology, clinical microbiology, and vaccine development, as they can be used to differentiate between different strains of bacteria and to develop vaccines that provide protection against specific bacterial infections.

Nippostrongylus is a genus of parasitic nematode (roundworm) that primarily infects the gastrointestinal tract of various mammalian hosts, including rodents and primates. The most common species that infects humans is Nippostrongylus brasiliensis, although it's not a common human parasite in normal circumstances. It is more frequently used in laboratory settings as a model organism to study immunology and host-parasite interactions.

The adult worms live in the alveoli of the lungs, where they mature and reproduce, releasing eggs that are coughed up, swallowed, and then hatch in the small intestine. The larvae then mature into adults and complete the life cycle. Infections can cause symptoms such as coughing, wheezing, abdominal pain, and diarrhea, but these are typically mild in immunocompetent individuals.

It's worth noting that human infections with Nippostrongylus are rare and usually occur in people who have close contact with infected animals or who consume contaminated food or water. Proper sanitation and hygiene practices can help prevent infection.

1. Receptors: In the context of physiology and medicine, receptors are specialized proteins found on the surface of cells or inside cells that detect and respond to specific molecules, known as ligands. These interactions can trigger a variety of responses within the cell, such as starting a signaling cascade or changing the cell's metabolism. Receptors play crucial roles in various biological processes, including communication between cells, regulation of immune responses, and perception of senses.

2. Antigen: An antigen is any substance (usually a protein) that can be recognized by the adaptive immune system, specifically by B-cells and T-cells. Antigens can be derived from various sources, such as microorganisms (like bacteria, viruses, or fungi), pollen, dust mites, or even components of our own cells (for instance, in autoimmune diseases). An antigen's ability to stimulate an immune response is determined by its molecular structure and whether it can be recognized by the receptors on immune cells.

3. B-Cell: B-cells are a type of white blood cell that plays a critical role in the adaptive immune system, particularly in humoral immunity. They originate from hematopoietic stem cells in the bone marrow and are responsible for producing antibodies, which are proteins that recognize and bind to specific antigens. Each B-cell has receptors on its surface called B-cell receptors (BCRs) that can recognize a unique antigen. When a B-cell encounters its specific antigen, it becomes activated, undergoes proliferation, and differentiates into plasma cells that secrete large amounts of antibodies to neutralize or eliminate the antigen.

Filariasis is a parasitic disease caused by infection with roundworms of the Filarioidea type. The infection is spread through the bite of infected mosquitoes and can lead to various symptoms depending on the type of filarial worm, including lymphatic dysfunction (elephantiasis), eye damage (onchocerciasis or river blindness), and tropical pulmonary eosinophilia. The disease is prevalent in tropical areas with poor sanitation and lack of access to clean water. Preventive measures include wearing protective clothing, using insect repellents, and sleeping under mosquito nets. Treatment typically involves the use of antiparasitic drugs such as diethylcarbamazine or ivermectin.

T-lymphocytes, also known as T-cells, are a type of white blood cell that plays a key role in the adaptive immune system's response to infection. They are produced in the bone marrow and mature in the thymus gland. There are several different types of T-cells, including CD4+ helper T-cells, CD8+ cytotoxic T-cells, and regulatory T-cells (Tregs).

CD4+ helper T-cells assist in activating other immune cells, such as B-lymphocytes and macrophages. They also produce cytokines, which are signaling molecules that help coordinate the immune response. CD8+ cytotoxic T-cells directly kill infected cells by releasing toxic substances. Regulatory T-cells help maintain immune tolerance and prevent autoimmune diseases by suppressing the activity of other immune cells.

T-lymphocytes are important in the immune response to viral infections, cancer, and other diseases. Dysfunction or depletion of T-cells can lead to immunodeficiency and increased susceptibility to infections. On the other hand, an overactive T-cell response can contribute to autoimmune diseases and chronic inflammation.

An Enzyme-Linked Immunosorbent Assay (ELISA) is a type of analytical biochemistry assay used to detect and quantify the presence of a substance, typically a protein or peptide, in a liquid sample. It takes its name from the enzyme-linked antibodies used in the assay.

In an ELISA, the sample is added to a well containing a surface that has been treated to capture the target substance. If the target substance is present in the sample, it will bind to the surface. Next, an enzyme-linked antibody specific to the target substance is added. This antibody will bind to the captured target substance if it is present. After washing away any unbound material, a substrate for the enzyme is added. If the enzyme is present due to its linkage to the antibody, it will catalyze a reaction that produces a detectable signal, such as a color change or fluorescence. The intensity of this signal is proportional to the amount of target substance present in the sample, allowing for quantification.

ELISAs are widely used in research and clinical settings to detect and measure various substances, including hormones, viruses, and bacteria. They offer high sensitivity, specificity, and reproducibility, making them a reliable choice for many applications.

Trematoda is a class of parasitic flatworms, also known as flukes. They have a complex life cycle involving one or more intermediate hosts and a definitive host. Adult trematodes are typically leaf-shaped and range in size from a few millimeters to several centimeters.

They have a characteristic oral sucker surrounding the mouth and a ventral sucker, which they use for locomotion and attachment to their host's tissues. Trematodes infect various organs of their hosts, including the liver, lungs, blood vessels, and intestines, causing a range of diseases in humans and animals.

Examples of human-infecting trematodes include Schistosoma spp., which cause schistosomiasis (also known as bilharzia), and Fasciola hepatica, which causes fascioliasis (liver fluke disease). Trematode infections are typically treated with antiparasitic drugs.

Tumor-associated carbohydrate antigens (TACAs) are a type of tumor antigen that are expressed on the surface of cancer cells. These antigens are abnormal forms of carbohydrates, also known as glycans, which are attached to proteins and lipids on the cell surface.

TACAs are often overexpressed or expressed in a different form on cancer cells compared to normal cells. This makes them attractive targets for cancer immunotherapy because they can be recognized by the immune system as foreign and elicit an immune response. Some examples of TACAs include gangliosides, fucosylated glycans, and sialylated glycans.

Tumor-associated carbohydrate antigens have been studied as potential targets for cancer vaccines, antibody therapies, and other immunotherapeutic approaches. However, their use as targets for cancer therapy is still in the early stages of research and development.

HLA-A2 antigen is a type of human leukocyte antigen (HLA) class I molecule, which is found on the surface of cells in our body. HLA molecules are responsible for presenting pieces of proteins (peptides) from inside the cell to the immune system's T-cells, helping them distinguish between "self" and "non-self" proteins.

HLA-A2 is one of the most common HLA class I antigens in the Caucasian population, with an estimated frequency of around 50%. It presents a variety of peptides to T-cells, including those derived from viruses and tumor cells. The presentation of these peptides can trigger an immune response, leading to the destruction of infected or malignant cells.

It is important to note that HLA typing is crucial in organ transplantation, as a mismatch between donor and recipient HLA antigens can lead to rejection of the transplanted organ. Additionally, HLA-A2 has been associated with certain autoimmune diseases and cancer types, making it an area of interest for researchers studying these conditions.

'Fasciola hepatica' is a medical term that refers to a type of flatworm, specifically a liver fluke, which is a parasitic flatworm that infects the livers of various animals, including sheep, cattle, and humans. The parasite has a complex life cycle involving aquatic snails as an intermediate host and can cause significant damage to the liver and bile ducts in its definitive host. Infection with Fasciola hepatica is known as fascioliasis, which can lead to symptoms such as abdominal pain, fever, and jaundice.

CD8 antigens are a type of protein found on the surface of certain immune cells called cytotoxic T lymphocytes or cytotoxic T cells. These cells play a critical role in the adaptive immune response, which is the specific and targeted response of the immune system to foreign substances (antigens) that invade the body.

CD8 antigens help cytotoxic T cells recognize and respond to infected or abnormal cells, such as those that have been infected by a virus or have become cancerous. When a cytotoxic T cell encounters a cell displaying a specific antigen bound to a CD8 molecule, it becomes activated and releases toxic substances that can kill the target cell.

CD8 antigens are also known as cluster of differentiation 8 antigens or CD8 receptors. They belong to a larger family of proteins called major histocompatibility complex class I (MHC class I) molecules, which present antigens to T cells and play a crucial role in the immune system's ability to distinguish between self and non-self.

Host-parasite interactions refer to the relationship between a parasitic organism (the parasite) and its host, which can be an animal, plant, or human body. The parasite lives on or inside the host and derives nutrients from it, often causing harm in the process. This interaction can range from relatively benign to severe, depending on various factors such as the species of the parasite, the immune response of the host, and the duration of infection.

The host-parasite relationship is often categorized based on the degree of harm caused to the host. Parasites that cause little to no harm are called commensals, while those that cause significant damage or disease are called parasitic pathogens. Some parasites can even manipulate their hosts' behavior and physiology to enhance their own survival and reproduction, leading to complex interactions between the two organisms.

Understanding host-parasite interactions is crucial for developing effective strategies to prevent and treat parasitic infections, as well as for understanding the ecological relationships between different species in natural ecosystems.

Th2 cells, or T helper 2 cells, are a type of CD4+ T cell that plays a key role in the immune response to parasites and allergens. They produce cytokines such as IL-4, IL-5, IL-13 which promote the activation and proliferation of eosinophils, mast cells, and B cells, leading to the production of antibodies such as IgE. Th2 cells also play a role in the pathogenesis of allergic diseases such as asthma, atopic dermatitis, and allergic rhinitis.

It's important to note that an imbalance in Th1/Th2 response can lead to immune dysregulation and disease states. For example, an overactive Th2 response can lead to allergic reactions while an underactive Th2 response can lead to decreased ability to fight off parasitic infections.

It's also worth noting that there are other subsets of CD4+ T cells such as Th1, Th17, Treg and others, each with their own specific functions and cytokine production profiles.

Helminth DNA refers to the genetic material found in parasitic worms that belong to the phylum Platyhelminthes (flatworms) and Nematoda (roundworms). These parasites can infect various organs and tissues of humans and animals, causing a range of diseases.

Helminths have complex life cycles involving multiple developmental stages and hosts. The study of their DNA has provided valuable insights into their evolutionary history, genetic diversity, and mechanisms of pathogenesis. It has also facilitated the development of molecular diagnostic tools for identifying and monitoring helminth infections.

Understanding the genetic makeup of these parasites is crucial for developing effective control strategies, including drug discovery, vaccine development, and disease management.

Cross reactions, in the context of medical diagnostics and immunology, refer to a situation where an antibody or a immune response directed against one antigen also reacts with a different antigen due to similarities in their molecular structure. This can occur in allergy testing, where a person who is allergic to a particular substance may have a positive test result for a different but related substance because of cross-reactivity between them. For example, some individuals who are allergic to birch pollen may also have symptoms when eating certain fruits, such as apples, due to cross-reactive proteins present in both.

Necator americanus is a species of parasitic hookworm that primarily infects the human intestine. The medical definition of Necator americanus would be:

A nematode (roundworm) of the family Ancylostomatidae, which is one of the most common causes of human hookworm infection worldwide. The adult worms live in the small intestine and feed on blood, causing iron deficiency anemia and protein loss. Infection occurs through contact with contaminated soil, often through bare feet, and results in a skin infection called cutaneous larva migrans (creeping eruption). After penetrating the skin, the larvae migrate to the lungs, ascend the respiratory tract, are swallowed, and then mature into adults in the small intestine.

The life cycle of Necator americanus involves several developmental stages, including eggs, larvae, and adult worms. The eggs are passed in the feces of infected individuals and hatch in warm, moist soil. The larvae then mature and become infective, able to penetrate human skin upon contact.

Preventive measures include wearing shoes in areas with known hookworm infection, avoiding walking barefoot on contaminated soil, improving sanitation and hygiene practices, and treating infected individuals to break the transmission cycle. Treatment of hookworm infection typically involves administration of anthelmintic medications, such as albendazole or mebendazole, which kill the adult worms in the intestine.

Trematode infections, also known as trematodiasis or fluke infections, are parasitic diseases caused by various species of flatworms called trematodes. These parasites have an indirect life cycle involving one or two intermediate hosts (such as snails or fish) and a definitive host (usually a mammal or bird).

Humans can become accidentally infected when they consume raw or undercooked aquatic plants, animals, or contaminated water that contains the larval stages of these parasites. The most common trematode infections affecting humans include:

1. Schistosomiasis (also known as bilharzia): Caused by several species of blood flukes (Schistosoma spp.). Adult worms live in the blood vessels, and their eggs can cause inflammation and damage to various organs, such as the liver, intestines, bladder, or lungs.
2. Liver flukes: Fasciola hepatica and Fasciola gigantica are common liver fluke species that infect humans through contaminated watercress or other aquatic plants. These parasites can cause liver damage, abdominal pain, diarrhea, and eosinophilia (elevated eosinophil count in the blood).
3. Lung flukes: Paragonimus spp. are lung fluke species that infect humans through consumption of raw or undercooked crustaceans. These parasites can cause coughing, chest pain, and bloody sputum.
4. Intestinal flukes: Various species of intestinal flukes (e.g., Haplorchis spp., Metagonimus yokogawai) infect humans through consumption of raw or undercooked fish. These parasites can cause abdominal pain, diarrhea, and eosinophilia.
5. Eye fluke: The oriental eye fluke (Drepanotrema spp.) can infect the human eye through contaminated water. It can cause eye inflammation, corneal ulcers, and vision loss.

Prevention measures include avoiding consumption of raw or undercooked aquatic plants, animals, and their products; practicing good hygiene; and treating drinking water to kill parasites. Treatment typically involves administering anthelmintic drugs such as praziquantel, albendazole, or mebendazole, depending on the specific fluke species involved.

Blood group antigens are molecular markers found on the surface of red blood cells (RBCs) and sometimes other types of cells in the body. These antigens are proteins, carbohydrates, or glycoproteins that can stimulate an immune response when foreign antigens are introduced into the body.

There are several different blood group systems, but the most well-known is the ABO system, which includes A, B, AB, and O blood groups. The antigens in this system are called ABO antigens. Individuals with type A blood have A antigens on their RBCs, those with type B blood have B antigens, those with type AB blood have both A and B antigens, and those with type O blood have neither A nor B antigens.

Another important blood group system is the Rh system, which includes the D antigen. Individuals who have this antigen are considered Rh-positive, while those who do not have it are considered Rh-negative.

Blood group antigens can cause complications during blood transfusions and pregnancy if there is a mismatch between the donor's or fetus's antigens and the recipient's antibodies. For example, if a person with type A blood receives type B blood, their anti-B antibodies will attack the foreign B antigens on the donated RBCs, causing a potentially life-threatening transfusion reaction. Similarly, if an Rh-negative woman becomes pregnant with an Rh-positive fetus, her immune system may produce anti-D antibodies that can cross the placenta and attack the fetal RBCs, leading to hemolytic disease of the newborn.

It is important for medical professionals to determine a patient's blood group before performing a transfusion or pregnancy-related procedures to avoid these complications.

Hepatitis B Surface Antigens (HBsAg) are proteins found on the surface of the Hepatitis B virus. They are present in the blood of individuals infected with the Hepatitis B virus and are used as a marker for the presence of a current Hepatitis B infection. The detection of HBsAg in the blood indicates that an individual is infectious and can transmit the virus to others. It is typically used in diagnostic tests to detect and diagnose Hepatitis B infections, monitor treatment response, and assess the risk of transmission.

CD3 antigens are a group of proteins found on the surface of T-cells, which are a type of white blood cell that plays a central role in the immune response. The CD3 antigens are composed of several different subunits (ε, δ, γ, and α) that associate to form the CD3 complex, which is involved in T-cell activation and signal transduction.

The CD3 complex is associated with the T-cell receptor (TCR), which recognizes and binds to specific antigens presented by antigen-presenting cells. When the TCR binds to an antigen, it triggers a series of intracellular signaling events that lead to T-cell activation and the initiation of an immune response.

CD3 antigens are important targets for immunotherapy in some diseases, such as certain types of cancer. For example, monoclonal antibodies that target CD3 have been developed to activate T-cells and enhance their ability to recognize and destroy tumor cells. However, CD3-targeted therapies can also cause side effects, such as cytokine release syndrome, which can be serious or life-threatening in some cases.

Lymphocyte activation is the process by which B-cells and T-cells (types of lymphocytes) become activated to perform effector functions in an immune response. This process involves the recognition of specific antigens presented on the surface of antigen-presenting cells, such as dendritic cells or macrophages.

The activation of B-cells leads to their differentiation into plasma cells that produce antibodies, while the activation of T-cells results in the production of cytotoxic T-cells (CD8+ T-cells) that can directly kill infected cells or helper T-cells (CD4+ T-cells) that assist other immune cells.

Lymphocyte activation involves a series of intracellular signaling events, including the binding of co-stimulatory molecules and the release of cytokines, which ultimately result in the expression of genes involved in cell proliferation, differentiation, and effector functions. The activation process is tightly regulated to prevent excessive or inappropriate immune responses that can lead to autoimmunity or chronic inflammation.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

I'm sorry for any confusion, but "soil" is not a term that has a medical definition. Soil is defined as the top layer of earth in which plants grow, a mixture of organic material, clay, sand, and silt. If you have any questions related to medicine or health, I would be happy to try to help answer them for you.

HLA-A antigens are a type of human leukocyte antigen (HLA) found on the surface of cells in our body. They are proteins that play an important role in the immune system by helping the body recognize and distinguish its own cells from foreign substances such as viruses, bacteria, and transplanted organs.

The HLA-A antigens are part of the major histocompatibility complex (MHC) class I molecules, which present peptide fragments from inside the cell to CD8+ T cells, also known as cytotoxic T lymphocytes (CTLs). The CTLs then recognize and destroy any cells that display foreign or abnormal peptides on their HLA-A antigens.

Each person has a unique set of HLA-A antigens, which are inherited from their parents. These antigens can vary widely between individuals, making it important to match HLA types in organ transplantation to reduce the risk of rejection. Additionally, certain HLA-A antigens have been associated with increased susceptibility or resistance to various diseases, including autoimmune disorders and infectious diseases.

Nematoda is a phylum of pseudocoelomate, unsegmented worms with a round or filiform body shape. They are commonly known as roundworms or threadworms. Nematodes are among the most diverse and numerous animals on earth, with estimates of over 1 million species, of which only about 25,000 have been described.

Nematodes are found in a wide range of habitats, including marine, freshwater, and terrestrial environments. Some nematode species are free-living, while others are parasitic, infecting a variety of hosts, including plants, animals, and humans. Parasitic nematodes can cause significant disease and economic losses in agriculture, livestock production, and human health.

The medical importance of nematodes lies primarily in their role as parasites that infect humans and animals. Some common examples of medically important nematodes include:

* Ascaris lumbricoides (human roundworm)
* Trichuris trichiura (whipworm)
* Ancylostoma duodenale and Necator americanus (hookworms)
* Enterobius vermicularis (pinworm or threadworm)
* Wuchereria bancrofti, Brugia malayi, and Loa loa (filarial nematodes that cause lymphatic filariasis, onchocerciasis, and loiasis, respectively)

Nematode infections can cause a range of clinical symptoms, depending on the species and the location of the parasite in the body. Common symptoms include gastrointestinal disturbances, anemia, skin rashes, and lymphatic swelling. In some cases, nematode infections can lead to serious complications or even death if left untreated.

Medical management of nematode infections typically involves the use of anthelmintic drugs, which are medications that kill or expel parasitic worms from the body. The choice of drug depends on the species of nematode and the severity of the infection. In some cases, preventive measures such as improved sanitation and hygiene can help reduce the risk of nematode infections.

Parasitic diseases are infections or illnesses caused by parasites, which are organisms that live and feed on host organisms, often causing harm. Parasites can be protozoans (single-celled organisms), helminths (worms), or ectoparasites (ticks, mites, fleas). These diseases can affect various body systems and cause a range of symptoms, depending on the type of parasite and the location of infection. They are typically spread through contaminated food or water, insect vectors, or direct contact with an infected host or contaminated environment. Examples of parasitic diseases include malaria, giardiasis, toxoplasmosis, ascariasis, and leishmaniasis.

"Taenia" is a genus of tapeworms that are known to infect humans and animals. The most common species that affect humans are Taenia saginata (beef tapeworm) and Taenia solium (pork tapeworm).

Humans can become infected with these tapeworms by consuming raw or undercooked meat from infected animals. Once inside the human body, the larvae can mature into adult tapeworms in the intestines, leading to a condition called taeniasis. Symptoms of taeniasis may include abdominal discomfort, diarrhea, and weight loss.

Ingesting eggs of Taenia solium, through contact with feces from an infected person or contaminated food, can lead to a more serious condition called cysticercosis, where larvae form cysts in various tissues throughout the body, including muscles, brain, and eyes. Cysticercosis can cause a range of symptoms depending on the location of the cysts, and it can be life-threatening if left untreated.

Preventive measures include cooking meat thoroughly, practicing good hygiene, and washing hands and food properly before eating.

"Trichinella spiralis" is a species of parasitic roundworm that causes the disease trichinosis in humans. The adult worms live in the intestine, where they produce larvae that migrate to striated muscle tissue, including the diaphragm, tongue, and skeletal muscles, where they encyst and form nurse cells. Infection typically occurs through the consumption of undercooked or raw meat, particularly pork, contaminated with the larvae. Symptoms can range from gastrointestinal disturbances to fever, muscle pain, and potentially life-threatening complications in severe cases. Prevention includes cooking meat thoroughly and freezing it at certain temperatures to kill the larvae.

Histocompatibility antigens, class I are proteins found on the surface of most cells in the body. They play a critical role in the immune system's ability to differentiate between "self" and "non-self." These antigens are composed of three polypeptides - two heavy chains and one light chain - and are encoded by genes in the major histocompatibility complex (MHC) on chromosome 6 in humans.

Class I MHC molecules present peptide fragments from inside the cell to CD8+ T cells, also known as cytotoxic T cells. This presentation allows the immune system to detect and destroy cells that have been infected by viruses or other intracellular pathogens, or that have become cancerous.

There are three main types of class I MHC molecules in humans: HLA-A, HLA-B, and HLA-C. The term "HLA" stands for human leukocyte antigen, which reflects the original identification of these proteins on white blood cells (leukocytes). The genes encoding these molecules are highly polymorphic, meaning there are many different variants in the population, and matching HLA types is essential for successful organ transplantation to minimize the risk of rejection.

Parasitology is a branch of biology that deals with the study of parasites, their life cycles, the relationship between parasites and their hosts, the transmission of parasitic diseases, and the development of methods for their control and elimination. It involves understanding various types of parasites including protozoa, helminths, and arthropods that can infect humans, animals, and plants. Parasitologists also study the evolution, genetics, biochemistry, and ecology of parasites to develop effective strategies for their diagnosis, treatment, and prevention.

"Strongyloides stercoralis" is a species of parasitic roundworm that can infect humans and other animals. The adult female worms live in the small intestine, where they lay eggs that hatch into larvae. These larvae can then either mature into adult worms within the host's intestine or be passed out of the body in feces. If the larvae in the feces come into contact with suitable moist soil, they can mature into infective larvae that can penetrate the skin of a new host and cause infection.

In humans, "Strongyloides stercoralis" infection can cause a range of symptoms, including abdominal pain, diarrhea, bloating, and weight loss. In some cases, the infection can become chronic and lead to serious complications, such as disseminated disease or gram-negative sepsis, particularly in individuals with weakened immune systems.

The diagnosis of "Strongyloides stercoralis" infection typically involves the detection of larvae in the stool or other bodily fluids, although serological tests and PCR assays are also available. Treatment usually involves the use of anti-parasitic drugs, such as ivermectin or albendazole, to kill the worms and prevent the progression of the infection.

HLA-D antigens, also known as HLA class II antigens, are a group of proteins found on the surface of cells that play an important role in the immune system. "HLA" stands for Human Leukocyte Antigen, which is a part of the major histocompatibility complex (MHC) in humans.

HLA-D antigens are primarily expressed by immune cells such as B lymphocytes, macrophages, and dendritic cells, but they can also be found on other cell types under certain conditions. These antigens help the immune system distinguish between "self" and "non-self" by presenting pieces of proteins (peptides) from both inside and outside the cell to T lymphocytes, a type of white blood cell that is crucial for mounting an immune response.

HLA-D antigens are divided into three subtypes: HLA-DP, HLA-DQ, and HLA-DR. Each subtype has a specific function in presenting peptides to T lymphocytes. The genes that encode HLA-D antigens are highly polymorphic, meaning there are many different variations of these genes in the population. This genetic diversity allows for a better match between an individual's immune system and the wide variety of pathogens they may encounter.

Abnormalities in HLA-D antigens have been associated with several autoimmune diseases, such as rheumatoid arthritis, type 1 diabetes, and multiple sclerosis. Additionally, certain variations in HLA-D genes can influence the severity of infectious diseases, such as HIV/AIDS and hepatitis C.

C57BL/6 (C57 Black 6) is an inbred strain of laboratory mouse that is widely used in biomedical research. The term "inbred" refers to a strain of animals where matings have been carried out between siblings or other closely related individuals for many generations, resulting in a population that is highly homozygous at most genetic loci.

The C57BL/6 strain was established in 1920 by crossing a female mouse from the dilute brown (DBA) strain with a male mouse from the black strain. The resulting offspring were then interbred for many generations to create the inbred C57BL/6 strain.

C57BL/6 mice are known for their robust health, longevity, and ease of handling, making them a popular choice for researchers. They have been used in a wide range of biomedical research areas, including studies of cancer, immunology, neuroscience, cardiovascular disease, and metabolism.

One of the most notable features of the C57BL/6 strain is its sensitivity to certain genetic modifications, such as the introduction of mutations that lead to obesity or impaired glucose tolerance. This has made it a valuable tool for studying the genetic basis of complex diseases and traits.

Overall, the C57BL/6 inbred mouse strain is an important model organism in biomedical research, providing a valuable resource for understanding the genetic and molecular mechanisms underlying human health and disease.

Antibody specificity refers to the ability of an antibody to bind to a specific epitope or antigenic determinant on an antigen. Each antibody has a unique structure that allows it to recognize and bind to a specific region of an antigen, typically a small portion of the antigen's surface made up of amino acids or sugar residues. This highly specific binding is mediated by the variable regions of the antibody's heavy and light chains, which form a pocket that recognizes and binds to the epitope.

The specificity of an antibody is determined by its unique complementarity-determining regions (CDRs), which are loops of amino acids located in the variable domains of both the heavy and light chains. The CDRs form a binding site that recognizes and interacts with the epitope on the antigen. The precise fit between the antibody's binding site and the epitope is critical for specificity, as even small changes in the structure of either can prevent binding.

Antibody specificity is important in immune responses because it allows the immune system to distinguish between self and non-self antigens. This helps to prevent autoimmune reactions where the immune system attacks the body's own cells and tissues. Antibody specificity also plays a crucial role in diagnostic tests, such as ELISA assays, where antibodies are used to detect the presence of specific antigens in biological samples.

Antigen receptors are specialized proteins found on the surface of immune cells, particularly B cells and T cells. These receptors are responsible for recognizing and binding to specific antigens, which are foreign substances such as proteins, carbohydrates, or lipids that stimulate an immune response.

B cell receptors (BCRs) are membrane-bound antibodies that recognize and bind to native antigens. When a BCR binds to its specific antigen, it triggers a series of intracellular signals that lead to the activation and differentiation of the B cell into an antibody-secreting plasma cell.

T cell receptors (TCRs) are membrane-bound proteins found on T cells that recognize and bind to antigens presented in the context of major histocompatibility complex (MHC) molecules on the surface of antigen-presenting cells. TCRs can distinguish between self and non-self antigens, allowing T cells to mount an immune response against infected or cancerous cells while sparing healthy cells.

Overall, antigen receptors play a critical role in the adaptive immune system's ability to recognize and respond to a wide variety of foreign substances.

Antibody formation, also known as humoral immune response, is the process by which the immune system produces proteins called antibodies in response to the presence of a foreign substance (antigen) in the body. This process involves several steps:

1. Recognition: The antigen is recognized and bound by a type of white blood cell called a B lymphocyte or B cell, which then becomes activated.
2. Differentiation: The activated B cell undergoes differentiation to become a plasma cell, which is a type of cell that produces and secretes large amounts of antibodies.
3. Antibody production: The plasma cells produce and release antibodies, which are proteins made up of four polypeptide chains (two heavy chains and two light chains) arranged in a Y-shape. Each antibody has two binding sites that can recognize and bind to specific regions on the antigen called epitopes.
4. Neutralization or elimination: The antibodies bind to the antigens, neutralizing them or marking them for destruction by other immune cells. This helps to prevent the spread of infection and protect the body from harmful substances.

Antibody formation is an important part of the adaptive immune response, which allows the body to specifically recognize and respond to a wide variety of pathogens and foreign substances.

CD45 is a protein that is found on the surface of many types of white blood cells, including T-cells, B-cells, and natural killer (NK) cells. It is also known as leukocyte common antigen because it is present on almost all leukocytes. CD45 is a tyrosine phosphatase that plays a role in regulating the activity of various proteins involved in cell signaling pathways.

As an antigen, CD45 is used as a marker to identify and distinguish different types of white blood cells. It has several isoforms that are generated by alternative splicing of its mRNA, resulting in different molecular weights. The size of the CD45 isoform can be used to distinguish between different subsets of T-cells and B-cells.

CD45 is an important molecule in the immune system, and abnormalities in its expression or function have been implicated in various diseases, including autoimmune disorders and cancer.

Hepatitis B antigens are proteins or particles present on the surface (HBsAg) or inside (HBcAg, HBeAg) the hepatitis B virus.

1. HBsAg (Hepatitis B surface antigen): This is a protein found on the outer surface of the hepatitis B virus. Its presence in the blood indicates an active infection with hepatitis B virus. It's also used as a marker to diagnose hepatitis B infection and monitor treatment response.

2. HBcAg (Hepatitis B core antigen): This is a protein found inside the hepatitis B virus core. It's not usually detected in the blood, but its antibodies (anti-HBc) are used to diagnose past or present hepatitis B infection.

3. HBeAg (Hepatitis B e antigen): This is a protein found inside the hepatitis B virus core and is associated with viral replication. Its presence in the blood indicates high levels of viral replication, increased infectivity, and higher risk of liver damage. It's used to monitor disease progression and treatment response.

These antigens play a crucial role in the diagnosis, management, and prevention of hepatitis B infection.

'Ascaris' is a genus of parasitic roundworms that are known to infect the human gastrointestinal tract. The two species that commonly infect humans are Ascaris lumbricoides (also known as the "large roundworm") and Ascaris suum (the "pig roundworm").

Human infection with Ascaris lumbricoides typically occurs through the ingestion of contaminated food or water containing the worm's eggs. Once inside the human body, these eggs hatch into larvae, which migrate through various tissues before reaching the small intestine, where they mature into adult worms. Adult female worms can grow up to 20-35 cm in length and produce thousands of eggs per day, which are then excreted in feces and can contaminate the environment, perpetuating the transmission cycle.

Symptoms of ascariasis (the infection caused by Ascaris) can range from mild to severe, depending on the number of worms present and the individual's overall health status. Light infections may not cause any symptoms, while heavy infections can lead to abdominal pain, nausea, vomiting, diarrhea, and intestinal obstruction. In some cases, Ascaris worms may migrate to unusual locations such as the lungs or bile ducts, causing additional complications.

Preventive measures include improving sanitation and hygiene practices, such as handwashing with soap and water, proper disposal of human feces, and cooking food thoroughly before consumption. Treatment typically involves administration of anthelmintic medications that kill the worms, followed by appropriate follow-up care to ensure complete eradication of the infection.

Hymenolepiasis is a parasitic infection caused by the tapeworms Hymenolepis nana (dwarf tapeworm) or Hymenolepis diminuta (rat tapeworm).

The dwarf tapeworm, H. nana, is the most common cause of hymenolepiasis and can complete its life cycle within a single host, making human-to-human transmission possible through the fecal-oral route. This means that eggs are ingested, often through contaminated food or water, and then hatched in the small intestine, where they develop into adult tapeworms.

On the other hand, H. diminuta requires an intermediate host, usually a rat or beetle, to complete its life cycle. Humans can become infected by ingesting the infected insect or contaminated food.

Symptoms of hymenolepiasis may include abdominal discomfort, diarrhea, loss of appetite, and weight loss. In severe cases, anemia and intestinal inflammation can occur. The infection is typically diagnosed through the identification of eggs or tapeworm segments in stool samples. Treatment usually involves administering a course of medication that targets the parasite, such as praziquantel or niclosamide.

CD4 antigens, also known as CD4 proteins or CD4 molecules, are a type of cell surface receptor found on certain immune cells, including T-helper cells and monocytes. They play a critical role in the immune response by binding to class II major histocompatibility complex (MHC) molecules on the surface of antigen-presenting cells and helping to activate T-cells. CD4 antigens are also the primary target of the human immunodeficiency virus (HIV), which causes AIDS, leading to the destruction of CD4-positive T-cells and a weakened immune system.

Immunoglobulin E (IgE) is a type of antibody that plays a key role in the immune response to parasitic infections and allergies. It is produced by B cells in response to stimulation by antigens, such as pollen, pet dander, or certain foods. Once produced, IgE binds to receptors on the surface of mast cells and basophils, which are immune cells found in tissues and blood respectively. When an individual with IgE antibodies encounters the allergen again, the cross-linking of IgE molecules bound to the FcεRI receptor triggers the release of mediators such as histamine, leukotrienes, prostaglandins, and various cytokines from these cells. These mediators cause the symptoms of an allergic reaction, such as itching, swelling, and redness. IgE also plays a role in protecting against certain parasitic infections by activating eosinophils, which can kill the parasites.

In summary, Immunoglobulin E (IgE) is a type of antibody that plays a crucial role in the immune response to allergens and parasitic infections, it binds to receptors on the surface of mast cells and basophils, when an individual with IgE antibodies encounters the allergen again, it triggers the release of mediators from these cells causing the symptoms of an allergic reaction.

Immunization is defined medically as the process where an individual is made immune or resistant to an infectious disease, typically through the administration of a vaccine. The vaccine stimulates the body's own immune system to recognize and fight off the specific disease-causing organism, thereby preventing or reducing the severity of future infections with that organism.

Immunization can be achieved actively, where the person is given a vaccine to trigger an immune response, or passively, where antibodies are transferred to the person through immunoglobulin therapy. Immunizations are an important part of preventive healthcare and have been successful in controlling and eliminating many infectious diseases worldwide.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

B-lymphocytes, also known as B-cells, are a type of white blood cell that plays a key role in the immune system's response to infection. They are responsible for producing antibodies, which are proteins that help to neutralize or destroy pathogens such as bacteria and viruses.

When a B-lymphocyte encounters a pathogen, it becomes activated and begins to divide and differentiate into plasma cells, which produce and secrete large amounts of antibodies specific to the antigens on the surface of the pathogen. These antibodies bind to the pathogen, marking it for destruction by other immune cells such as neutrophils and macrophages.

B-lymphocytes also have a role in presenting antigens to T-lymphocytes, another type of white blood cell involved in the immune response. This helps to stimulate the activation and proliferation of T-lymphocytes, which can then go on to destroy infected cells or help to coordinate the overall immune response.

Overall, B-lymphocytes are an essential part of the adaptive immune system, providing long-lasting immunity to previously encountered pathogens and helping to protect against future infections.

An antigen-antibody reaction is a specific immune response that occurs when an antigen (a foreign substance, such as a protein or polysaccharide on the surface of a bacterium or virus) comes into contact with a corresponding antibody (a protective protein produced by the immune system in response to the antigen). The antigen and antibody bind together, forming an antigen-antibody complex. This interaction can neutralize the harmful effects of the antigen, mark it for destruction by other immune cells, or activate complement proteins to help eliminate the antigen from the body. Antigen-antibody reactions are a crucial part of the adaptive immune response and play a key role in the body's defense against infection and disease.

CD1 antigens are a group of molecules found on the surface of certain immune cells, including dendritic cells and B cells. They play a role in the immune system by presenting lipid antigens to T cells, which helps initiate an immune response against foreign substances such as bacteria and viruses. CD1 molecules are distinct from other antigen-presenting molecules like HLA because they present lipids rather than peptides. There are five different types of CD1 molecules (CD1a, CD1b, CD1c, CD1d, and CD1e) that differ in their tissue distribution and the types of lipid antigens they present.

Necatoriasis is a parasitic infection caused by the nematode (roundworm) Necator americanus, also known as the "New World hookworm." This condition is primarily found in areas with warm, moist climates and poor sanitation. The infection typically occurs when the larvae of the parasite penetrate the skin, usually through bare feet that come into contact with contaminated soil.

Once inside the human body, the larvae migrate to the lungs, where they mature and are coughed up and swallowed. They then reside in the small intestine, where they feed on blood and cause symptoms such as abdominal pain, diarrhea, anemia, and growth retardation in children. Necatoriasis is usually treated with anthelmintic medications like albendazole or mebendazole. Preventive measures include wearing shoes in areas where the parasite is common and improving sanitation to reduce the spread of contaminated soil.

The Fluorescent Antibody Technique (FAT) is a type of immunofluorescence assay used in laboratory medicine and pathology for the detection and localization of specific antigens or antibodies in tissues, cells, or microorganisms. In this technique, a fluorescein-labeled antibody is used to selectively bind to the target antigen or antibody, forming an immune complex. When excited by light of a specific wavelength, the fluorescein label emits light at a longer wavelength, typically visualized as green fluorescence under a fluorescence microscope.

The FAT is widely used in diagnostic microbiology for the identification and characterization of various bacteria, viruses, fungi, and parasites. It has also been applied in the diagnosis of autoimmune diseases and certain cancers by detecting specific antibodies or antigens in patient samples. The main advantage of FAT is its high sensitivity and specificity, allowing for accurate detection and differentiation of various pathogens and disease markers. However, it requires specialized equipment and trained personnel to perform and interpret the results.

Bacterial antibodies are a type of antibodies produced by the immune system in response to an infection caused by bacteria. These antibodies are proteins that recognize and bind to specific antigens on the surface of the bacterial cells, marking them for destruction by other immune cells. Bacterial antibodies can be classified into several types based on their structure and function, including IgG, IgM, IgA, and IgE. They play a crucial role in the body's defense against bacterial infections and provide immunity to future infections with the same bacteria.

'Immune sera' refers to the serum fraction of blood that contains antibodies produced in response to an antigenic stimulus, such as a vaccine or an infection. These antibodies are proteins known as immunoglobulins, which are secreted by B cells (a type of white blood cell) and can recognize and bind to specific antigens. Immune sera can be collected from an immunized individual and used as a source of passive immunity to protect against infection or disease. It is often used in research and diagnostic settings to identify or measure the presence of specific antigens or antibodies.

Strongyloidiasis is a tropical and subtropical parasitic disease caused by the nematode (roundworm) Strongyloides stercoralis. The infection occurs when the larvae of this parasite penetrate the skin, usually of the feet, and are carried through the bloodstream to the lungs. Here they mature, are coughed up and swallowed, and then mature in the small intestine where they lay eggs. These hatch into larvae that can either pass out with the feces or penetrate the skin of the anal area and restart the cycle.

The disease is often asymptomatic but can cause a range of symptoms including gastrointestinal (diarrhea, abdominal pain) and pulmonary (cough, wheezing) symptoms. Disseminated strongyloidiasis, where the larvae spread throughout the body, can occur in immunocompromised individuals and can be life-threatening.

Treatment is with anti-parasitic drugs such as ivermectin or thiabendazole. Prevention involves avoiding skin contact with contaminated soil and good hygiene practices.

HLA-B antigens are human leukocyte antigen (HLA) proteins found on the surface of cells that play an important role in the body's immune system. They are part of the major histocompatibility complex (MHC) class I molecules, which present pieces of proteins from inside the cell to T-cells, a type of white blood cell involved in immune responses.

HLA-B antigens are highly polymorphic, meaning that there are many different variations or alleles of this gene in the human population. This genetic diversity allows for a wide range of potential HLA-B proteins to be expressed, which can help recognize and respond to a variety of foreign substances, such as viruses and cancer cells.

The HLA-B antigens are inherited from both parents, and an individual may express one or two different HLA-B antigens depending on their genetic makeup. The specific combination of HLA-B antigens that a person expresses can have implications for their susceptibility to certain diseases, as well as their compatibility with organ transplants.

Dendritic cells (DCs) are a type of immune cell that play a critical role in the body's defense against infection and cancer. They are named for their dendrite-like projections, which they use to interact with and sample their environment. DCs are responsible for processing antigens (foreign substances that trigger an immune response) and presenting them to T cells, a type of white blood cell that plays a central role in the immune system's response to infection and cancer.

DCs can be found throughout the body, including in the skin, mucous membranes, and lymphoid organs. They are able to recognize and respond to a wide variety of antigens, including those from bacteria, viruses, fungi, and parasites. Once they have processed an antigen, DCs migrate to the lymph nodes, where they present the antigen to T cells. This interaction activates the T cells, which then go on to mount a targeted immune response against the invading pathogen or cancerous cells.

DCs are a diverse group of cells that can be divided into several subsets based on their surface markers and function. Some DCs, such as Langerhans cells and dermal DCs, are found in the skin and mucous membranes, where they serve as sentinels for invading pathogens. Other DCs, such as plasmacytoid DCs and conventional DCs, are found in the lymphoid organs, where they play a role in activating T cells and initiating an immune response.

Overall, dendritic cells are essential for the proper functioning of the immune system, and dysregulation of these cells has been implicated in a variety of diseases, including autoimmune disorders and cancer.

Strongyloidea is a superfamily of parasitic nematode (roundworm) worms that includes several medically important genera such as Strongyloides and Rhabditis. These parasites are known to infect humans and other animals, causing a variety of symptoms depending on the species and the location of the infection in the body.

The genus Strongyloides contains several species that can infect humans, including S. stercoralis, S. fuelleborni, and S. kellyi. These parasites are known to cause strongyloidiasis, a disease characterized by gastrointestinal symptoms such as abdominal pain, diarrhea, and bloating, as well as skin rashes and respiratory symptoms in some cases.

The life cycle of Strongyloides species is complex and involves both free-living and parasitic stages. The worms can infect humans through contact with contaminated soil or water, and can then reproduce within the human body, causing ongoing infection and potentially serious complications if left untreated.

Treatment for strongyloidiasis typically involves administration of anti-parasitic drugs such as ivermectin or albendazole, which can help to eliminate the infection and prevent further transmission.

Antigens are substances (usually proteins) on the surface of cells, viruses, fungi, or bacteria that can be recognized by the immune system and provoke an immune response. In the context of differentiation, antigens refer to specific markers that identify the developmental stage or lineage of a cell.

Differentiation antigens are proteins or carbohydrates expressed on the surface of cells during various stages of differentiation, which can be used to distinguish between cells at different maturation stages or of different cell types. These antigens play an essential role in the immune system's ability to recognize and respond to abnormal or infected cells while sparing healthy cells.

Examples of differentiation antigens include:

1. CD (cluster of differentiation) molecules: A group of membrane proteins used to identify and define various cell types, such as T cells, B cells, natural killer cells, monocytes, and granulocytes.
2. Lineage-specific antigens: Antigens that are specific to certain cell lineages, such as CD3 for T cells or CD19 for B cells.
3. Maturation markers: Antigens that indicate the maturation stage of a cell, like CD34 and CD38 on hematopoietic stem cells.

Understanding differentiation antigens is crucial in immunology, cancer research, transplantation medicine, and vaccine development.

Trichinellosis is a parasitic disease caused by the roundworm Trichinella spiralis. The infection typically occurs when contaminated raw or undercooked meat, often pork, is consumed. After ingestion, the larvae of the worm are released from the cysts in the meat and migrate to the small intestine, where they mature into adults.

The adult females then lay new larvae that penetrate the intestinal wall and travel through the bloodstream to striated muscle tissue (such as skeletal muscles), where they encapsulate and form new cysts. The symptoms of trichinellosis can vary widely, depending on the number of worms ingested and the intensity of infection. Early symptoms may include diarrhea, abdominal pain, nausea, vomiting, and fever. As the larvae migrate to muscle tissue, additional symptoms such as muscle pain, weakness, swelling of the face, eyelids, or tongue, and skin rashes can occur. Severe infections may lead to life-threatening complications, including heart and respiratory failure.

Prevention measures include cooking meat thoroughly (to an internal temperature of at least 160°F or 71°C), freezing meat properly (at -15°F or -26°C for several days) to kill the parasites, and avoiding consumption of raw or undercooked meat, especially from wild animals.

A cell line is a culture of cells that are grown in a laboratory for use in research. These cells are usually taken from a single cell or group of cells, and they are able to divide and grow continuously in the lab. Cell lines can come from many different sources, including animals, plants, and humans. They are often used in scientific research to study cellular processes, disease mechanisms, and to test new drugs or treatments. Some common types of human cell lines include HeLa cells (which come from a cancer patient named Henrietta Lacks), HEK293 cells (which come from embryonic kidney cells), and HUVEC cells (which come from umbilical vein endothelial cells). It is important to note that cell lines are not the same as primary cells, which are cells that are taken directly from a living organism and have not been grown in the lab.

Mebendazole is a medication used to treat various types of worm infections, such as roundworm, whipworm, hookworm, and threadworm. It belongs to a class of drugs called anthelmintics, which work by preventing the worms from absorbing nutrients, leading to their eventual death and elimination from the body.

Mebendazole is available in various forms, including tablets, chewable tablets, and suspensions. It is usually taken as a single dose or for several days, depending on the type and severity of the infection being treated.

It's important to note that mebendazole is not effective against all types of worm infections, so it should only be used under the guidance and supervision of a healthcare professional. Additionally, while taking mebendazole, it's recommended to maintain good hygiene practices, such as washing hands frequently and avoiding contaminated food or water, to prevent reinfection.

A helminth genome refers to the complete set of genetic information present in the DNA of a helminth organism. Helminths are parasitic worms that include nematodes (roundworms), cestodes (tapeworms), and trematodes (flukes). The genome of a helminth includes all of the genes that code for proteins, as well as non-coding DNA sequences that regulate gene expression and other functions.

The study of helminth genomics has provided important insights into the biology and evolution of these parasites, as well as their interactions with their hosts. For example, genomic studies have identified potential drug targets and vaccine candidates, and have helped to elucidate the mechanisms of host-parasite coevolution.

It's worth noting that the size and complexity of helminth genomes can vary widely depending on the species. Some helminth genomes are relatively small and compact, while others are large and complex, with a high degree of genetic diversity. The human whipworm (Trichuris trichiura), for example, has a genome size of approximately 120 megabases, while the tapeworm Schistosoma mansoni has a genome size of over 360 megabases.

Overall, the study of helminth genomics is an important area of research that has the potential to inform the development of new strategies for preventing and treating helminth infections, which affect millions of people worldwide.

Prevalence, in medical terms, refers to the total number of people in a given population who have a particular disease or condition at a specific point in time, or over a specified period. It is typically expressed as a percentage or a ratio of the number of cases to the size of the population. Prevalence differs from incidence, which measures the number of new cases that develop during a certain period.

MART-1, also known as Melanoma Antigen Recognized by T-Cells 1 or Melan-A, is a protein that is primarily found in melanocytes, which are the pigment-producing cells located in the skin, eyes, and hair follicles. It is a member of the family of antigens called melanoma differentiation antigens (MDAs) that are specifically expressed in melanocytes and melanomas. MART-1 is considered a tumor-specific antigen because it is overexpressed in melanoma cells compared to normal cells, making it an attractive target for immunotherapy.

MART-1 is presented on the surface of melanoma cells in complex with major histocompatibility complex (MHC) class I molecules, where it can be recognized by cytotoxic T lymphocytes (CTLs). This recognition triggers an immune response that can lead to the destruction of melanoma cells. MART-1 has been widely used as a target in various immunotherapy approaches, including cancer vaccines and adoptive cell transfer therapies, with the goal of enhancing the body's own immune system to recognize and eliminate melanoma cells.

The spleen is an organ in the upper left side of the abdomen, next to the stomach and behind the ribs. It plays multiple supporting roles in the body:

1. It fights infection by acting as a filter for the blood. Old red blood cells are recycled in the spleen, and platelets and white blood cells are stored there.
2. The spleen also helps to control the amount of blood in the body by removing excess red blood cells and storing platelets.
3. It has an important role in immune function, producing antibodies and removing microorganisms and damaged red blood cells from the bloodstream.

The spleen can be removed without causing any significant problems, as other organs take over its functions. This is known as a splenectomy and may be necessary if the spleen is damaged or diseased.

Interferon-gamma (IFN-γ) is a soluble cytokine that is primarily produced by the activation of natural killer (NK) cells and T lymphocytes, especially CD4+ Th1 cells and CD8+ cytotoxic T cells. It plays a crucial role in the regulation of the immune response against viral and intracellular bacterial infections, as well as tumor cells. IFN-γ has several functions, including activating macrophages to enhance their microbicidal activity, increasing the presentation of major histocompatibility complex (MHC) class I and II molecules on antigen-presenting cells, stimulating the proliferation and differentiation of T cells and NK cells, and inducing the production of other cytokines and chemokines. Additionally, IFN-γ has direct antiproliferative effects on certain types of tumor cells and can enhance the cytotoxic activity of immune cells against infected or malignant cells.

Antiparasitic agents are a type of medication used to treat parasitic infections. These agents include a wide range of drugs that work to destroy, inhibit the growth of, or otherwise eliminate parasites from the body. Parasites are organisms that live on or inside a host and derive nutrients at the host's expense.

Antiparasitic agents can be divided into several categories based on the type of parasite they target. Some examples include:

* Antimalarial agents: These drugs are used to treat and prevent malaria, which is caused by a parasite that is transmitted through the bites of infected mosquitoes.
* Antiprotozoal agents: These drugs are used to treat infections caused by protozoa, which are single-celled organisms that can cause diseases such as giardiasis, amoebic dysentery, and sleeping sickness.
* Antihelminthic agents: These drugs are used to treat infections caused by helminths, which are parasitic worms that can infect various organs of the body, including the intestines, lungs, and skin. Examples include roundworms, tapeworms, and flukes.

Antiparasitic agents work in different ways to target parasites. Some disrupt the parasite's metabolism or interfere with its ability to reproduce. Others damage the parasite's membrane or exoskeleton, leading to its death. The specific mechanism of action depends on the type of antiparasitic agent and the parasite it is targeting.

It is important to note that while antiparasitic agents can be effective in treating parasitic infections, they can also have side effects and potential risks. Therefore, it is essential to consult with a healthcare provider before starting any antiparasitic medication to ensure safe and appropriate use.

"Cells, cultured" is a medical term that refers to cells that have been removed from an organism and grown in controlled laboratory conditions outside of the body. This process is called cell culture and it allows scientists to study cells in a more controlled and accessible environment than they would have inside the body. Cultured cells can be derived from a variety of sources, including tissues, organs, or fluids from humans, animals, or cell lines that have been previously established in the laboratory.

Cell culture involves several steps, including isolation of the cells from the tissue, purification and characterization of the cells, and maintenance of the cells in appropriate growth conditions. The cells are typically grown in specialized media that contain nutrients, growth factors, and other components necessary for their survival and proliferation. Cultured cells can be used for a variety of purposes, including basic research, drug development and testing, and production of biological products such as vaccines and gene therapies.

It is important to note that cultured cells may behave differently than they do in the body, and results obtained from cell culture studies may not always translate directly to human physiology or disease. Therefore, it is essential to validate findings from cell culture experiments using additional models and ultimately in clinical trials involving human subjects.

Taeniasis is a parasitic infection caused by the tapeworm of the genus Taenia. The two most common species that infect humans are Taenia saginata (beef tapeworm) and Taenia solium (pork tapeworm).

Humans get infected with T. saginata by consuming raw or undercooked beef from cattle that carry the larval form of the tapeworm, called cysticercus. In contrast, humans acquire T. solium through the consumption of contaminated pork or, more commonly, by accidentally ingesting T. solium eggs due to poor hygiene practices, leading to a more severe infection known as cysticercosis.

After ingestion, the larvae develop into adult tapeworms in the human intestine, where they can grow up to 8-12 meters long for T. saginata and 2-3 meters for T. solium. Adult tapeworms consist of a head (scolex) with hooks and suckers that attach to the intestinal wall, a neck region where new segments called proglottids are continuously formed, and a chain of mature proglottids containing male and female reproductive organs.

Symptoms of taeniasis can be mild or even absent, but they may include abdominal discomfort, diarrhea, nausea, weight loss, and the presence of proglottids or tapeworm segments in stools or, rarely, outside the body (e.g., around the anus). In cases of T. solium infection, accidental ingestion of eggs can lead to cysticercosis, which is a more severe condition involving the formation of larval cysts in various tissues, including muscles, brain, and eyes, causing neurological symptoms and potentially life-threatening complications.

Diagnosis of taeniasis typically involves microscopic examination of stool samples to identify tapeworm eggs or proglottids. In some cases, molecular techniques like PCR may be used for species identification. Treatment usually consists of a single oral dose of anthelmintic medication such as praziquantel or niclosamide, which eliminates the adult tapeworm from the intestine. Proper sanitation and hygiene measures are crucial to prevent transmission and reinfection.

Hymenolepis nana, also known as the dwarf tapeworm, is a small intestine-infecting cestode parasite that primarily affects humans and rodents. The adult worms are typically 15-40 mm in length and have a scolex (head) with four suckers but no hooks. The proglottids (segments) of the worm contain both male and female reproductive organs, allowing for self-fertilization.

The life cycle of Hymenolepis nana can be direct or indirect. In the direct life cycle, eggs are passed in the feces of an infected individual and ingested by another person through contaminated food, water, or fomites (inanimate objects). Once inside the human host, the eggs hatch in the small intestine, releasing oncospheres that invade the intestinal wall and develop into cysticercoids. The cysticercoids then mature into adult tapeworms within 10-15 days.

In the indirect life cycle, eggs are ingested by an intermediate host, usually a beetle or flea, where they hatch and develop into cysticercoids. When the infected insect is consumed by a rodent or human, the cysticercoids excyst in the small intestine and mature into adult tapeworms.

Symptoms of Hymenolepis nana infection can range from mild to severe and may include abdominal discomfort, diarrhea, loss of appetite, weight loss, and anemia. In some cases, particularly in children or individuals with weakened immune systems, the infection can lead to more serious complications such as intestinal obstruction or inflammation of the small intestine (enteritis).

Praziquantel is an anthelmintic medication, which is used to treat and prevent trematode (fluke) infections, including schistosomiasis (also known as bilharzia or snail fever), clonorchiasis, opisthorchiasis, paragonimiasis, and fasciolopsiasis. It works by causing severe spasms in the muscle cells of the parasites, ultimately leading to their death. Praziquantel is available in tablet form and is typically taken orally in a single dose, although the dosage may vary depending on the type and severity of the infection being treated.

It's important to note that praziquantel is not effective against tapeworm infections, and other medications such as niclosamide or albendazole are used instead for those infections. Also, Praziquantel should be taken under medical supervision, as it may have some side effects, including abdominal pain, nausea, vomiting, dizziness, and headache.

It's important to consult a healthcare professional before taking any medication.

'Ascaris suum' is a species of roundworm that primarily infects pigs, although it can also rarely infect humans. It is a type of parasitic nematode that lives in the intestines of its host and obtains nutrients from ingested food. The adult female worm can grow up to 40 cm in length and produces thousands of eggs every day. These eggs are passed in the feces of infected animals and can survive in the environment for years, making them a significant source of infection for other pigs or humans who come into contact with them.

In pigs, 'Ascaris suum' infection can cause a range of symptoms, including diarrhea, vomiting, and stunted growth. In severe cases, it can lead to intestinal blockages or pneumonia. Humans who become infected with 'Ascaris suum' typically experience milder symptoms, such as abdominal pain, coughing, and wheezing. However, in rare cases, the infection can cause more serious complications, particularly if the worms migrate to other parts of the body.

Preventing 'Ascaris suum' infection involves good hygiene practices, such as washing hands thoroughly after handling animals or coming into contact with soil that may contain infected feces. It is also important to properly cook pork before eating it and to avoid consuming raw or undercooked meat. In areas where 'Ascaris suum' is common, deworming programs for pigs can help reduce the risk of infection for both animals and humans.

HIV antigens refer to the proteins present on the surface or within the human immunodeficiency virus (HIV), which can stimulate an immune response in the infected individual. These antigens are recognized by the host's immune system, specifically by CD4+ T cells and antibodies, leading to their activation and production. Two significant HIV antigens are the HIV-1 p24 antigen and the gp120/gp41 envelope proteins. The p24 antigen is a capsid protein found within the viral particle, while the gp120/gp41 complex forms the viral envelope and facilitates viral entry into host cells. Detection of HIV antigens in clinical settings, such as in the ELISA or Western blot tests, helps diagnose HIV infection and monitor disease progression.

A parasite is an organism that lives on or in a host organism and gets its sustenance at the expense of the host. Parasites are typically much smaller than their hosts, and they may be classified as either ectoparasites (which live on the outside of the host's body) or endoparasites (which live inside the host's body).

Parasites can cause a range of health problems in humans, depending on the type of parasite and the extent of the infection. Some parasites may cause only mild symptoms or none at all, while others can lead to serious illness or even death. Common symptoms of parasitic infections include diarrhea, abdominal pain, weight loss, and fatigue.

There are many different types of parasites that can infect humans, including protozoa (single-celled organisms), helminths (worms), and ectoparasites (such as lice and ticks). Parasitic infections are more common in developing countries with poor sanitation and hygiene, but they can also occur in industrialized nations.

Preventing parasitic infections typically involves practicing good hygiene, such as washing hands regularly, cooking food thoroughly, and avoiding contaminated water. Treatment for parasitic infections usually involves medication to kill the parasites and relieve symptoms.

CD80 (also known as B7-1) is a cell surface protein that functions as a costimulatory molecule in the immune system. It is primarily expressed on antigen presenting cells such as dendritic cells, macrophages, and B cells. CD80 binds to the CD28 receptor on T cells, providing a critical second signal necessary for T cell activation and proliferation. This interaction plays a crucial role in the initiation of an effective immune response against pathogens and tumors.

CD80 can also interact with another receptor called CTLA-4 (cytotoxic T lymphocyte antigen 4), which is expressed on activated T cells. The binding of CD80 to CTLA-4 delivers a negative signal that helps regulate the immune response and prevent overactivation, contributing to the maintenance of self-tolerance and preventing autoimmunity.

In summary, CD80 is an important antigen involved in the regulation of the adaptive immune response by modulating T cell activation and proliferation through its interactions with CD28 and CTLA-4 receptors.

Fascioliasis is a parasitic infection caused by two species of flatworms (trematodes) called Fasciola hepatica and Fasciola gigantica. These worms are commonly known as liver flukes. The infection occurs when people consume raw or undercooked watercress, watercress salad, or other contaminated vegetables.

The life cycle of these parasites involves a complex series of stages involving snails and aquatic vegetation. When humans ingest the larval stage of the parasite, it migrates through the intestinal wall, enters the abdominal cavity, and eventually reaches the liver. Here, it causes damage to the bile ducts and liver parenchyma, leading to symptoms such as fever, abdominal pain, diarrhea, and jaundice.

Fascioliasis is more common in areas where livestock farming is prevalent, particularly in parts of South America, Africa, and Asia. However, it can also occur in travelers who have consumed contaminated food or water while visiting endemic areas. Treatment typically involves the use of anti-parasitic medications such as triclabendazole or praziquantel.

Flow cytometry is a medical and research technique used to measure physical and chemical characteristics of cells or particles, one cell at a time, as they flow in a fluid stream through a beam of light. The properties measured include:

* Cell size (light scatter)
* Cell internal complexity (granularity, also light scatter)
* Presence or absence of specific proteins or other molecules on the cell surface or inside the cell (using fluorescent antibodies or other fluorescent probes)

The technique is widely used in cell counting, cell sorting, protein engineering, biomarker discovery and monitoring disease progression, particularly in hematology, immunology, and cancer research.

Ancylostoma is a genus of parasitic roundworms that are commonly known as hookworms. These intestinal parasites infect humans and other animals through contact with contaminated soil, often via the skin or mouth. Two species of Ancylostoma that commonly infect humans are Ancylostoma duodenale and Ancylostoma ceylanicum.

Ancylostoma duodenale is found primarily in tropical and subtropical regions, including parts of the Mediterranean, Africa, Asia, and southern Europe. It can cause a disease called ancylostomiasis or hookworm infection, which can lead to symptoms such as abdominal pain, diarrhea, anemia, and impaired growth in children.

Ancylostoma ceylanicum is found mainly in Southeast Asia, southern China, and some parts of Australia. It can also cause ancylostomiasis, with symptoms similar to those caused by Ancylostoma duodenale. However, Ancylostoma ceylanicum infections are often less severe than those caused by Ancylostoma duodenale.

Preventive measures for hookworm infection include wearing shoes in areas where the soil may be contaminated with feces, washing hands thoroughly after using the toilet or handling soil, and avoiding ingestion of contaminated soil or water. Treatment for hookworm infection typically involves administration of anthelmintic drugs to eliminate the parasites from the body.

Ovalbumin is the major protein found in egg white, making up about 54-60% of its total protein content. It is a glycoprotein with a molecular weight of around 45 kDa and has both hydrophilic and hydrophobic regions. Ovalbumin is a single polypeptide chain consisting of 385 amino acids, including four disulfide bridges that contribute to its structure.

Ovalbumin is often used in research as a model antigen for studying immune responses and allergies. In its native form, ovalbumin is not allergenic; however, when it is denatured or degraded into smaller peptides through cooking or digestion, it can become an allergen for some individuals.

In addition to being a food allergen, ovalbumin has been used in various medical and research applications, such as vaccine development, immunological studies, and protein structure-function analysis.

Cytokines are a broad and diverse category of small signaling proteins that are secreted by various cells, including immune cells, in response to different stimuli. They play crucial roles in regulating the immune response, inflammation, hematopoiesis, and cellular communication.

Cytokines mediate their effects by binding to specific receptors on the surface of target cells, which triggers intracellular signaling pathways that ultimately result in changes in gene expression, cell behavior, and function. Some key functions of cytokines include:

1. Regulating the activation, differentiation, and proliferation of immune cells such as T cells, B cells, natural killer (NK) cells, and macrophages.
2. Coordinating the inflammatory response by recruiting immune cells to sites of infection or tissue damage and modulating their effector functions.
3. Regulating hematopoiesis, the process of blood cell formation in the bone marrow, by controlling the proliferation, differentiation, and survival of hematopoietic stem and progenitor cells.
4. Modulating the development and function of the nervous system, including neuroinflammation, neuroprotection, and neuroregeneration.

Cytokines can be classified into several categories based on their structure, function, or cellular origin. Some common types of cytokines include interleukins (ILs), interferons (IFNs), tumor necrosis factors (TNFs), chemokines, colony-stimulating factors (CSFs), and transforming growth factors (TGFs). Dysregulation of cytokine production and signaling has been implicated in various pathological conditions, such as autoimmune diseases, chronic inflammation, cancer, and neurodegenerative disorders.

Coinfection is a term used in medicine to describe a situation where a person is infected with more than one pathogen (infectious agent) at the same time. This can occur when a person is infected with two or more viruses, bacteria, parasites, or fungi. Coinfections can complicate the diagnosis and treatment of infectious diseases, as the symptoms of each infection can overlap and interact with each other.

Coinfections are common in certain populations, such as people who are immunocompromised, have chronic illnesses, or live in areas with high levels of infectious agents. For example, a person with HIV/AIDS may be more susceptible to coinfections with tuberculosis, hepatitis, or pneumocystis pneumonia. Similarly, a person who has recently undergone an organ transplant may be at risk for coinfections with cytomegalovirus, Epstein-Barr virus, or other opportunistic pathogens.

Coinfections can also occur in people who are otherwise healthy but are exposed to multiple infectious agents at once, such as through travel to areas with high levels of infectious diseases or through close contact with animals that carry infectious agents. For example, a person who travels to a tropical area may be at risk for coinfections with malaria and dengue fever, while a person who works on a farm may be at risk for coinfections with influenza and Q fever.

Effective treatment of coinfections requires accurate diagnosis and appropriate antimicrobial therapy for each pathogen involved. In some cases, treating one infection may help to resolve the other, but in other cases, both infections may need to be treated simultaneously to achieve a cure. Preventing coinfections is an important part of infectious disease control, and can be achieved through measures such as vaccination, use of personal protective equipment, and avoidance of high-risk behaviors.

Epstein-Barr virus nuclear antigens (EBV NA) are proteins found inside the nucleus of cells that have been infected with the Epstein-Barr virus (EBV). EBV is a type of herpesvirus that is best known as the cause of infectious mononucleosis (also known as "mono" or "the kissing disease").

There are two main types of EBV NA: EBNA-1 and EBNA-2. These proteins play a role in the replication and survival of the virus within infected cells. They can be detected using laboratory tests, such as immunofluorescence assays or Western blotting, to help diagnose EBV infection or detect the presence of EBV-associated diseases, such as certain types of lymphoma and nasopharyngeal carcinoma.

EBNA-1 is essential for the maintenance and replication of the EBV genome within infected cells, while EBNA-2 activates viral gene expression and modulates the host cell's immune response to promote virus survival. Both proteins are considered potential targets for the development of antiviral therapies and vaccines against EBV infection.

"Schistosoma haematobium" is a species of parasitic flatworm, also known as a blood fluke, that causes the disease schistosomiasis (also known as bilharzia). This specific species is the most common cause of urogenital schistosomiasis.

The life cycle of Schistosoma haematobium involves freshwater snails as intermediate hosts. The parasite's eggs are released in the urine of an infected person and hatch in fresh water, releasing miracidia that infect the snail. After several developmental stages, the parasites emerge from the snail as free-swimming cercariae, which then infect the human host by penetrating the skin during contact with infested water.

Once inside the human body, the cercariae transform into schistosomula and migrate to the venous plexus around the bladder, where they mature into adult worms. The female worms lay eggs that can cause inflammation and damage to the urinary tract and, in some cases, other organs. Symptoms of infection can include blood in the urine, frequent urination, and pain during urination. Chronic infection can lead to more serious complications, such as bladder cancer and kidney damage.

Immunoenzyme techniques are a group of laboratory methods used in immunology and clinical chemistry that combine the specificity of antibody-antigen reactions with the sensitivity and amplification capabilities of enzyme reactions. These techniques are primarily used for the detection, quantitation, or identification of various analytes (such as proteins, hormones, drugs, viruses, or bacteria) in biological samples.

In immunoenzyme techniques, an enzyme is linked to an antibody or antigen, creating a conjugate. This conjugate then interacts with the target analyte in the sample, forming an immune complex. The presence and amount of this immune complex can be visualized or measured by detecting the enzymatic activity associated with it.

There are several types of immunoenzyme techniques, including:

1. Enzyme-linked Immunosorbent Assay (ELISA): A widely used method for detecting and quantifying various analytes in a sample. In ELISA, an enzyme is attached to either the capture antibody or the detection antibody. After the immune complex formation, a substrate is added that reacts with the enzyme, producing a colored product that can be measured spectrophotometrically.
2. Immunoblotting (Western blot): A method used for detecting specific proteins in a complex mixture, such as a protein extract from cells or tissues. In this technique, proteins are separated by gel electrophoresis and transferred to a membrane, where they are probed with an enzyme-conjugated antibody directed against the target protein.
3. Immunohistochemistry (IHC): A method used for detecting specific antigens in tissue sections or cells. In IHC, an enzyme-conjugated primary or secondary antibody is applied to the sample, and the presence of the antigen is visualized using a chromogenic substrate that produces a colored product at the site of the antigen-antibody interaction.
4. Immunofluorescence (IF): A method used for detecting specific antigens in cells or tissues by employing fluorophore-conjugated antibodies. The presence of the antigen is visualized using a fluorescence microscope.
5. Enzyme-linked immunosorbent assay (ELISA): A method used for detecting and quantifying specific antigens or antibodies in liquid samples, such as serum or culture supernatants. In ELISA, an enzyme-conjugated detection antibody is added after the immune complex formation, and a substrate is added that reacts with the enzyme to produce a colored product that can be measured spectrophotometrically.

These techniques are widely used in research and diagnostic laboratories for various applications, including protein characterization, disease diagnosis, and monitoring treatment responses.

CD4-positive T-lymphocytes, also known as CD4+ T cells or helper T cells, are a type of white blood cell that plays a crucial role in the immune response. They express the CD4 receptor on their surface and help coordinate the immune system's response to infectious agents such as viruses and bacteria.

CD4+ T cells recognize and bind to specific antigens presented by antigen-presenting cells, such as dendritic cells or macrophages. Once activated, they can differentiate into various subsets of effector cells, including Th1, Th2, Th17, and Treg cells, each with distinct functions in the immune response.

CD4+ T cells are particularly important in the immune response to HIV (human immunodeficiency virus), which targets and destroys these cells, leading to a weakened immune system and increased susceptibility to opportunistic infections. The number of CD4+ T cells is often used as a marker of disease progression in HIV infection, with lower counts indicating more advanced disease.

Cellular immunity, also known as cell-mediated immunity, is a type of immune response that involves the activation of immune cells, such as T lymphocytes (T cells), to protect the body against infected or damaged cells. This form of immunity is important for fighting off infections caused by viruses and intracellular bacteria, as well as for recognizing and destroying cancer cells.

Cellular immunity involves a complex series of interactions between various immune cells and molecules. When a pathogen infects a cell, the infected cell displays pieces of the pathogen on its surface in a process called antigen presentation. This attracts T cells, which recognize the antigens and become activated. Activated T cells then release cytokines, chemicals that help coordinate the immune response, and can directly attack and kill infected cells or help activate other immune cells to do so.

Cellular immunity is an important component of the adaptive immune system, which is able to learn and remember specific pathogens in order to mount a faster and more effective response upon subsequent exposure. This form of immunity is also critical for the rejection of transplanted organs, as the immune system recognizes the transplanted tissue as foreign and attacks it.

CD19 is a type of protein found on the surface of B cells, which are a type of white blood cell that plays a key role in the body's immune response. CD19 is a marker that helps identify and distinguish B cells from other types of cells in the body. It is also a target for immunotherapy in certain diseases, such as B-cell malignancies.

An antigen is any substance that can stimulate an immune response, particularly the production of antibodies. In the context of CD19, antigens refer to substances that can bind to CD19 and trigger a response from the immune system. This can include proteins, carbohydrates, or other molecules found on the surface of bacteria, viruses, or cancer cells.

Therefore, 'antigens, CD19' refers to any substances that can bind to the CD19 protein on B cells and trigger an immune response. These antigens may be used in the development of immunotherapies for the treatment of B-cell malignancies or other diseases.

Antigen-presenting cells (APCs) are a group of specialized cells in the immune system that play a critical role in initiating and regulating immune responses. They have the ability to engulf, process, and present antigens (molecules derived from pathogens or other foreign substances) on their surface in conjunction with major histocompatibility complex (MHC) molecules. This presentation of antigens allows APCs to activate T cells, which are crucial for adaptive immunity.

There are several types of APCs, including:

1. Dendritic cells (DCs): These are the most potent and professional APCs, found in various tissues throughout the body. DCs can capture antigens from their environment, process them, and migrate to lymphoid organs where they present antigens to T cells.
2. Macrophages: These large phagocytic cells are found in many tissues and play a role in both innate and adaptive immunity. They can engulf and digest pathogens, then present processed antigens on their MHC class II molecules to activate CD4+ T helper cells.
3. B cells: These are primarily responsible for humoral immune responses by producing antibodies against antigens. When activated, B cells can also function as APCs and present antigens on their MHC class II molecules to CD4+ T cells.

The interaction between APCs and T cells is critical for the development of an effective immune response against pathogens or other foreign substances. This process helps ensure that the immune system can recognize and eliminate threats while minimizing damage to healthy tissues.

Wuchereria bancrofti is a parasitic roundworm that causes lymphatic filariasis, also known as elephantiasis. It is transmitted to humans through the bite of infected mosquitoes. The worms infect the lymphatic system and can lead to chronic swelling of body parts such as the limbs, breasts, and genitals, as well as other symptoms including fever, chills, and skin rashes. Wuchereria bancrofti is a significant public health problem in many tropical and subtropical regions around the world.

Interleukin-4 (IL-4) is a type of cytokine, which is a cell signaling molecule that mediates communication between cells in the immune system. Specifically, IL-4 is produced by activated T cells and mast cells, among other cells, and plays an important role in the differentiation and activation of immune cells called Th2 cells.

Th2 cells are involved in the immune response to parasites, as well as in allergic reactions. IL-4 also promotes the growth and survival of B cells, which produce antibodies, and helps to regulate the production of certain types of antibodies. In addition, IL-4 has anti-inflammatory effects and can help to downregulate the immune response in some contexts.

Defects in IL-4 signaling have been implicated in a number of diseases, including asthma, allergies, and certain types of cancer.

Heterophile antigens are a type of antigen that can induce an immune response in multiple species, not just the one they originate from. They are called "heterophile" because they exhibit cross-reactivity with antibodies produced against different antigens from other species. A common example of heterophile antigens is the Forssman antigen, which can be found in various animals such as guinea pigs, rabbits, and humans.

Heterophile antibody tests are often used in diagnostic medicine to detect certain infections or autoimmune disorders. One well-known example is the Paul-Bunnell test, which was historically used to diagnose infectious mononucleosis (IM) caused by the Epstein-Barr virus (EBV). The test detects heterophile antibodies produced against EBV antigens that cross-react with sheep red blood cells. However, this test has been largely replaced by more specific and sensitive EBV antibody tests.

It is important to note that heterophile antibody tests can sometimes produce false positive results due to the presence of these cross-reactive antibodies in individuals who have not been infected with the targeted pathogen. Therefore, it is crucial to interpret test results cautiously and consider them alongside clinical symptoms, medical history, and other diagnostic findings.

Toxocariasis is a parasitic infection caused by the roundworms Toxocara canis or Toxocara cati, which are found in the intestines of dogs and cats, respectively. Humans become infected through the accidental ingestion of infective eggs from contaminated soil, water, or food. The larvae hatch in the small intestine and migrate to various tissues, including the liver, lungs, eyes, and central nervous system, where they can cause inflammation and damage.

The severity of the infection depends on the number of larvae that have infected the body and the organs involved. Most infections are asymptomatic or mild, causing symptoms such as fever, cough, rash, or abdominal discomfort. However, in severe cases, toxocariasis can lead to serious complications, including blindness (ocular larva migrans) or neurological damage (visceral larva migrans).

Preventive measures include good hygiene practices, such as washing hands after handling soil or pets, and avoiding contact with dog or cat feces. Regular deworming of pets can also help reduce the risk of transmission.

Hepatitis B core antigen (HBcAg) is a protein found in the core of the hepatitis B virus (HBV). It is present during active replication of the virus and plays a crucial role in the formation of the viral capsid or core. The antibodies produced against HBcAg (anti-HBc) can be detected in the blood, which serves as a marker for current or past HBV infection. It is important to note that HBcAg itself is not detectable in the blood because it is confined within the viral particle. However, during the serological testing of hepatitis B, the detection of anti-HBc IgM indicates a recent acute infection, while the presence of anti-HBc IgG suggests either a past resolved infection or an ongoing chronic infection.

Hymenolepis is a genus of tapeworms that are commonly found in rodents and other small mammals, but can also infect humans. The two species that are most relevant to human health are Hymenolepis nana and Hymenolepis diminuta.

Hymenolepis nana, also known as the dwarf tapeworm, is the smallest tapeworm that infects humans. It is unique among tapeworms because it can complete its entire life cycle within a single host, without needing an intermediate host. This means that it can be transmitted directly from person to person through contaminated food or water.

Hymenolepis diminuta, on the other hand, requires an intermediate host, such as a beetle or grain moth, to complete its life cycle. Humans can become infected by accidentally ingesting these insects, which may be found in contaminated grains or other food products.

Both species of Hymenolepis can cause similar symptoms in humans, including abdominal pain, diarrhea, and weight loss. In severe cases, they can also lead to more serious complications such as intestinal obstruction or nutritional deficiencies.

It's worth noting that while Hymenolepis infections are not uncommon in certain parts of the world, they are relatively rare in developed countries with good sanitation and hygiene practices. Treatment typically involves taking medication to kill the tapeworms, such as niclosamide or praziquantel.

CD40 is a type of protein known as a tumor necrosis factor receptor that is found on the surface of various cells in the body, including B cells, dendritic cells, and activated T cells. It plays an important role in the immune system by interacting with another protein called CD154 (also known as CD40 ligand) to activate immune responses.

CD40 antigens are molecules that can stimulate an immune response when introduced into the body because they are recognized as foreign substances by the immune system. They may be used in vaccines or other immunotherapies to induce an immune response against specific targets, such as cancer cells or infectious agents.

CD40 antigens can also be found on some types of tumor cells, and activating CD40 with CD154 has been shown to enhance the anti-tumor immune response in preclinical models. Therefore, CD40 agonists are being investigated as potential cancer therapies.

In summary, CD40 antigens are proteins that can stimulate an immune response and are involved in activating immune cells. They have potential applications in vaccines, immunotherapies, and cancer treatments.

Immunodiffusion is a laboratory technique used in immunology to detect and measure the presence of specific antibodies or antigens in a sample. It is based on the principle of diffusion, where molecules move from an area of high concentration to an area of low concentration until they reach equilibrium. In this technique, a sample containing an unknown quantity of antigen or antibody is placed in a gel or agar medium that contains a known quantity of antibody or antigen, respectively.

The two substances then diffuse towards each other and form a visible precipitate at the point where they meet and reach equivalence, which indicates the presence and quantity of the specific antigen or antibody in the sample. There are several types of immunodiffusion techniques, including radial immunodiffusion (RID) and double immunodiffusion (Ouchterlony technique). These techniques are widely used in diagnostic laboratories to identify and measure various antigens and antibodies, such as those found in infectious diseases, autoimmune disorders, and allergic reactions.

Autoantigens are substances that are typically found in an individual's own body, but can stimulate an immune response because they are recognized as foreign by the body's own immune system. In autoimmune diseases, the immune system mistakenly attacks and damages healthy tissues and organs because it recognizes some of their components as autoantigens. These autoantigens can be proteins, DNA, or other molecules that are normally present in the body but have become altered or exposed due to various factors such as infection, genetics, or environmental triggers. The immune system then produces antibodies and activates immune cells to attack these autoantigens, leading to tissue damage and inflammation.

Basophils are a type of white blood cell that are part of the immune system. They are granulocytes, which means they contain granules filled with chemicals that can be released in response to an infection or inflammation. Basophils are relatively rare, making up less than 1% of all white blood cells.

When basophils become activated, they release histamine and other chemical mediators that can contribute to allergic reactions, such as itching, swelling, and redness. They also play a role in inflammation, helping to recruit other immune cells to the site of an infection or injury.

Basophils can be identified under a microscope based on their characteristic staining properties. They are typically smaller than other granulocytes, such as neutrophils and eosinophils, and have a multi-lobed nucleus with dark purple-staining granules in the cytoplasm.

While basophils play an important role in the immune response, abnormal levels of basophils can be associated with various medical conditions, such as allergies, infections, and certain types of leukemia.

Antibodies are proteins produced by the immune system in response to the presence of a foreign substance, such as a bacterium or virus. They are capable of identifying and binding to specific antigens (foreign substances) on the surface of these invaders, marking them for destruction by other immune cells. Antibodies are also known as immunoglobulins and come in several different types, including IgA, IgD, IgE, IgG, and IgM, each with a unique function in the immune response. They are composed of four polypeptide chains, two heavy chains and two light chains, that are held together by disulfide bonds. The variable regions of the heavy and light chains form the antigen-binding site, which is specific to a particular antigen.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

To the best of my knowledge, "Côte d'Ivoire" is not a medical term or concept. It is the name of a country, which is officially known as the Republic of Côte d'Ivoire. The country is located in West Africa and is bordered by countries such as Ghana, Mali, Burkina Faso, and Liberia.

Côte d'Ivoire was once a French colony and gained its independence in 1960. The country has a diverse population and a developing economy, with agriculture being a major contributor to its GDP. The capital city of Côte d'Ivoire is Yamoussoukro, while the largest city is Abidjan.

It's important to note that medical terminology and concepts are typically related to anatomy, physiology, diseases, treatments, and other health-related topics. Therefore, it's unlikely that a country name like Côte d'Ivoire would have a direct medical definition or application.

Immunoglobulin M (IgM) is a type of antibody that is primarily found in the blood and lymph fluid. It is the first antibody to be produced in response to an initial exposure to an antigen, making it an important part of the body's primary immune response. IgM antibodies are large molecules that are composed of five basic units, giving them a pentameric structure. They are primarily found on the surface of B cells as membrane-bound immunoglobulins (mlgM), where they function as receptors for antigens. Once an mlgM receptor binds to an antigen, it triggers the activation and differentiation of the B cell into a plasma cell that produces and secretes large amounts of soluble IgM antibodies.

IgM antibodies are particularly effective at agglutination (clumping) and complement activation, which makes them important in the early stages of an immune response to help clear pathogens from the bloodstream. However, they are not as stable or long-lived as other types of antibodies, such as IgG, and their levels tend to decline after the initial immune response has occurred.

In summary, Immunoglobulin M (IgM) is a type of antibody that plays a crucial role in the primary immune response to antigens by agglutination and complement activation. It is primarily found in the blood and lymph fluid, and it is produced by B cells after they are activated by an antigen.

Mansonelliasis is a parasitic infection caused by the nematode (roundworm) species Mansonella perstans, M. ozzardi, or M. streptocerca. These parasites are transmitted to humans through the bite of infected blackflies or midges. The infection can cause a range of symptoms including fever, headache, pruritus (severe itching), and rash. In some cases, there may be no symptoms at all. Chronic infections can lead to more serious complications such as endocarditis, hepatomegaly (enlarged liver), and splenomegaly (enlarged spleen). However, mansonelliasis is often overlooked or misdiagnosed due to its nonspecific symptoms and the limited availability of diagnostic tests.

Thy-1, also known as Thy-1 antigen or CD90, is a glycosylphosphatidylinositol (GPI)-anchored protein found on the surface of various cells in the body. It was first discovered as a cell surface antigen on thymocytes, hence the name Thy-1.

Thy-1 is a member of the immunoglobulin superfamily and is widely expressed in different tissues, including the brain, where it is found on the surface of neurons and glial cells. In the immune system, Thy-1 is expressed on the surface of T lymphocytes, natural killer (NK) cells, and some subsets of dendritic cells.

The function of Thy-1 is not fully understood, but it has been implicated in various biological processes, including cell adhesion, signal transduction, and regulation of immune responses. Thy-1 has also been shown to play a role in the development and maintenance of the nervous system, as well as in the pathogenesis of certain neurological disorders.

As an antigen, Thy-1 can be recognized by specific antibodies, which can be used in various research and clinical applications, such as immunohistochemistry, flow cytometry, and cell sorting.

The Forssman antigen is a type of heterophile antigen, which is a substance that can stimulate an immune response in animals of different species. It was first discovered by the Swedish bacteriologist, John Forssman, in 1911. The Forssman antigen is found in a variety of tissues and organs, including the kidney, liver, and brain, in many different animal species, including humans.

The Forssman antigen is unique because it can induce the production of antibodies that cross-react with tissues from other species. This means that an immune response to the Forssman antigen in one species can also recognize and react with similar antigens in another species, leading to the possibility of cross-species immune reactions.

The Forssman antigen is a complex glycosphingolipid molecule that is found on the surface of cells. It is not clear what role, if any, the Forssman antigen plays in normal physiological processes. However, its presence has been implicated in various disease processes, including autoimmune disorders and transplant rejection.

In summary, the Forssman antigen is a heterophile antigen found in a variety of tissues and organs in many different animal species, including humans. It can induce cross-reacting antibodies and has been implicated in various disease processes.

An antigen-antibody complex is a type of immune complex that forms when an antibody binds to a specific antigen. An antigen is any substance that triggers an immune response, while an antibody is a protein produced by the immune system to neutralize or destroy foreign substances like antigens.

When an antibody binds to an antigen, it forms a complex that can be either soluble or insoluble. Soluble complexes are formed when the antigen is small and can move freely through the bloodstream. Insoluble complexes, on the other hand, are formed when the antigen is too large to move freely, such as when it is part of a bacterium or virus.

The formation of antigen-antibody complexes plays an important role in the immune response. Once formed, these complexes can be recognized and cleared by other components of the immune system, such as phagocytes, which help to prevent further damage to the body. However, in some cases, the formation of large numbers of antigen-antibody complexes can lead to inflammation and tissue damage, contributing to the development of certain autoimmune diseases.

Spiruroidea is a taxonomic category of parasitic nematodes (roundworms) that belong to the phylum Nematoda. These parasites are primarily found in the gastrointestinal tract of various vertebrate hosts, including mammals, birds, reptiles, and amphibians. They have a complex life cycle involving one or more intermediate hosts, often arthropods such as beetles or crustaceans.

Spiruroids are characterized by their long, slender bodies with distinct anterior and posterior ends. The mouth is surrounded by three lips, and they possess a muscular esophagus that is typically divided into two parts: a narrow anterior portion called the stoma, and a wider posterior portion called the bulb.

Some well-known examples of Spiruroidea include the genus Spirura, which parasitizes carnivores and birds; the genus Habronema, which infects horses and other herbivores; and the genus Thelazia, which causes eye infections in humans and animals.

It is important to note that taxonomy is a dynamic field, and the classification of Spiruroidea may change as new research and discoveries emerge.

The H-Y antigen is a complex of historically significant, male-specific proteins that are encoded by genes on the Y chromosome. These antigens were first discovered through studies of tissue rejection in animal models and were later found to be important in the field of transplantation immunology.

In a medical definition, the H-Y antigen refers to a group of antigens that are expressed on the cell surface of nucleated cells in males, including those found in tissues such as skin, muscle, and blood cells. They are recognized by the immune system as foreign when transplanted into females, leading to a rejection response.

The H-Y antigen has been the subject of extensive research due to its role in sex determination and differentiation, as well as its potential implications for autoimmune diseases and cancer biology. However, it's worth noting that the clinical relevance of the H-Y antigen is limited, and its study is primarily of academic interest.

A vaccine is a biological preparation that provides active acquired immunity to a particular infectious disease. It typically contains an agent that resembles the disease-causing microorganism and is often made from weakened or killed forms of the microbe, its toxins, or one of its surface proteins. The agent stimulates the body's immune system to recognize the agent as a threat, destroy it, and "remember" it, so that the immune system can more easily recognize and destroy any of these microorganisms that it encounters in the future.

Vaccines can be prophylactic (to prevent or ameliorate the effects of a future infection by a natural or "wild" pathogen), or therapeutic (to fight disease that is already present). The administration of vaccines is called vaccination. Vaccinations are generally administered through needle injections, but can also be administered by mouth or sprayed into the nose.

The term "vaccine" comes from Edward Jenner's 1796 use of cowpox to create immunity to smallpox. The first successful vaccine was developed in 1796 by Edward Jenner, who showed that milkmaids who had contracted cowpox did not get smallpox. He reasoned that exposure to cowpox protected against smallpox and tested his theory by injecting a boy with pus from a cowpox sore and then exposing him to smallpox, which the boy did not contract. The word "vaccine" is derived from Variolae vaccinae (smallpox of the cow), the term devised by Jenner to denote cowpox. He used it in 1798 during a conversation with a fellow physician and later in the title of his 1801 Inquiry.

I'm sorry for any confusion, but "Schistosomiasis haematobia" is not a recognized medical term. Schistosomiasis is a parasitic disease caused by several species of blood flukes (schistosomes). The two main forms that affect humans are Schistosoma mansoni and Schistosoma haematobium, but the term "haematobia" itself refers to the presence of blood in urine.

So, when we talk about Schistosoma haematobium, it's a specific species of schistosome that causes an infection known as urogenital schistosomiasis, which is characterized by the presence of blood in the urine (haematuria) and other symptoms.

If you have any questions about tropical diseases or parasitic infections, feel free to ask!

Molecular weight, also known as molecular mass, is the mass of a molecule. It is expressed in units of atomic mass units (amu) or daltons (Da). Molecular weight is calculated by adding up the atomic weights of each atom in a molecule. It is a useful property in chemistry and biology, as it can be used to determine the concentration of a substance in a solution, or to calculate the amount of a substance that will react with another in a chemical reaction.

Lymphocytes are a type of white blood cell that is an essential part of the immune system. They are responsible for recognizing and responding to potentially harmful substances such as viruses, bacteria, and other foreign invaders. There are two main types of lymphocytes: B-lymphocytes (B-cells) and T-lymphocytes (T-cells).

B-lymphocytes produce antibodies, which are proteins that help to neutralize or destroy foreign substances. When a B-cell encounters a foreign substance, it becomes activated and begins to divide and differentiate into plasma cells, which produce and secrete large amounts of antibodies. These antibodies bind to the foreign substance, marking it for destruction by other immune cells.

T-lymphocytes, on the other hand, are involved in cell-mediated immunity. They directly attack and destroy infected cells or cancerous cells. T-cells can also help to regulate the immune response by producing chemical signals that activate or inhibit other immune cells.

Lymphocytes are produced in the bone marrow and mature in either the bone marrow (B-cells) or the thymus gland (T-cells). They circulate throughout the body in the blood and lymphatic system, where they can be found in high concentrations in lymph nodes, the spleen, and other lymphoid organs.

Abnormalities in the number or function of lymphocytes can lead to a variety of immune-related disorders, including immunodeficiency diseases, autoimmune disorders, and cancer.

Complement fixation tests are a type of laboratory test used in immunology and serology to detect the presence of antibodies in a patient's serum. These tests are based on the principle of complement activation, which is a part of the immune response. The complement system consists of a group of proteins that work together to help eliminate pathogens from the body.

In a complement fixation test, the patient's serum is mixed with a known antigen and complement proteins. If the patient has antibodies against the antigen, they will bind to it and activate the complement system. This results in the consumption or "fixation" of the complement proteins, which are no longer available to participate in a secondary reaction.

A second step involves adding a fresh source of complement proteins and a dye-labeled antibody that recognizes a specific component of the complement system. If complement was fixed during the first step, it will not be available for this secondary reaction, and the dye-labeled antibody will remain unbound. Conversely, if no antibodies were present in the patient's serum, the complement proteins would still be available for the second reaction, leading to the binding of the dye-labeled antibody.

The mixture is then examined under a microscope or using a spectrophotometer to determine whether the dye-labeled antibody has bound. If it has not, this indicates that the patient's serum contains antibodies specific to the antigen used in the test, and a positive result is recorded.

Complement fixation tests have been widely used for the diagnosis of various infectious diseases, such as syphilis, measles, and influenza. However, they have largely been replaced by more modern serological techniques, like enzyme-linked immunosorbent assays (ELISAs) and nucleic acid amplification tests (NAATs), due to their increased sensitivity, specificity, and ease of use.

HLA-DQ antigens are a type of human leukocyte antigen (HLA) that are found on the surface of cells in our body. They are a part of the major histocompatibility complex (MHC) class II molecules, which play a crucial role in the immune system by presenting pieces of proteins from outside the cell to CD4+ T cells, also known as helper T cells. This presentation process is essential for initiating an appropriate immune response against potentially harmful pathogens such as bacteria and viruses.

HLA-DQ antigens are encoded by genes located on chromosome 6p21.3 in the HLA region. Each individual inherits a pair of HLA-DQ genes, one from each parent, which can result in various combinations of HLA-DQ alleles. These genetic variations contribute to the diversity of immune responses among different individuals.

HLA-DQ antigens consist of two noncovalently associated polypeptide chains: an alpha (DQA) chain and a beta (DQB) chain. There are several isotypes of HLA-DQ antigens, including DQ1, DQ2, DQ3, DQ4, DQ5, DQ6, DQ7, DQ8, and DQ9, which are determined by the specific combination of DQA and DQB alleles.

Certain HLA-DQ genotypes have been associated with an increased risk of developing certain autoimmune diseases, such as celiac disease (DQ2 and DQ8), type 1 diabetes (DQ2, DQ8), and rheumatoid arthritis (DQ4). Understanding the role of HLA-DQ antigens in these conditions can provide valuable insights into disease pathogenesis and potential therapeutic targets.

CD86 is a type of protein found on the surface of certain immune cells called antigen-presenting cells (APCs), such as dendritic cells, macrophages, and B cells. These proteins are known as co-stimulatory molecules and play an important role in activating T cells, a type of white blood cell that is crucial for adaptive immunity.

When APCs encounter a pathogen or foreign substance, they engulf it, break it down into smaller peptides, and display these peptides on their surface in conjunction with another protein called the major histocompatibility complex (MHC) class II molecule. This presentation of antigenic peptides to T cells is not sufficient to activate them fully. Instead, APCs must also provide a co-stimulatory signal through interactions between co-stimulatory molecules like CD86 and receptors on the surface of T cells, such as CD28.

CD86 binds to its receptor CD28 on T cells, providing a critical second signal that promotes T cell activation, proliferation, and differentiation into effector cells. This interaction is essential for the development of an effective immune response against pathogens or foreign substances. In addition to its role in activating T cells, CD86 also helps regulate immune tolerance by contributing to the suppression of self-reactive T cells that could otherwise attack the body's own tissues and cause autoimmune diseases.

Overall, CD86 is an important player in the regulation of the immune response, helping to ensure that T cells are activated appropriately in response to pathogens or foreign substances while also contributing to the maintenance of self-tolerance.

Simian Virus 40 (SV40) is a polyomavirus that is found in both monkeys and humans. It is a DNA virus that has been extensively studied in laboratory settings due to its ability to transform cells and cause tumors in animals. In fact, SV40 was discovered as a contaminant of poliovirus vaccines that were prepared using rhesus monkey kidney cells in the 1950s and 1960s.

SV40 is not typically associated with human disease, but there has been some concern that exposure to the virus through contaminated vaccines or other means could increase the risk of certain types of cancer, such as mesothelioma and brain tumors. However, most studies have failed to find a consistent link between SV40 infection and cancer in humans.

The medical community generally agrees that SV40 is not a significant public health threat, but researchers continue to study the virus to better understand its biology and potential impact on human health.

Recombinant proteins are artificially created proteins produced through the use of recombinant DNA technology. This process involves combining DNA molecules from different sources to create a new set of genes that encode for a specific protein. The resulting recombinant protein can then be expressed, purified, and used for various applications in research, medicine, and industry.

Recombinant proteins are widely used in biomedical research to study protein function, structure, and interactions. They are also used in the development of diagnostic tests, vaccines, and therapeutic drugs. For example, recombinant insulin is a common treatment for diabetes, while recombinant human growth hormone is used to treat growth disorders.

The production of recombinant proteins typically involves the use of host cells, such as bacteria, yeast, or mammalian cells, which are engineered to express the desired protein. The host cells are transformed with a plasmid vector containing the gene of interest, along with regulatory elements that control its expression. Once the host cells are cultured and the protein is expressed, it can be purified using various chromatography techniques.

Overall, recombinant proteins have revolutionized many areas of biology and medicine, enabling researchers to study and manipulate proteins in ways that were previously impossible.

Strongyloides is a type of parasitic roundworm that can infect humans and other animals. The most common species to infect humans is Strongyloides stercoralis. These tiny worms can cause a condition known as strongyloidiasis, which can lead to symptoms such as abdominal pain, diarrhea, and skin rashes.

The life cycle of Strongyloides is unique among parasitic roundworms because it can complete its entire life cycle within a single host, without needing to exit the body and infect a new host. This is known as "autoinfection" and it allows the worm to persist in the human body for many years, even in the absence of new infections.

Strongyloides infection typically occurs when larvae (immature worms) penetrate the skin, often through contaminated soil. The larvae then travel through the bloodstream to the lungs, where they mature and are coughed up and swallowed, allowing them to reach the intestines and mature into adults. Female adult worms can lay eggs that hatch into larvae, which can either be excreted in feces or undergo autoinfection by penetrating the intestinal wall and entering the bloodstream again.

While many people with Strongyloides infection do not experience any symptoms, severe infections can lead to complications such as chronic diarrhea, malnutrition, and bacterial bloodstream infections. In immunocompromised individuals, Strongyloides infection can be life-threatening due to the rapid multiplication of larvae in the body, a condition known as "hyperinfection."

Sensitivity and specificity are statistical measures used to describe the performance of a diagnostic test or screening tool in identifying true positive and true negative results.

* Sensitivity refers to the proportion of people who have a particular condition (true positives) who are correctly identified by the test. It is also known as the "true positive rate" or "recall." A highly sensitive test will identify most or all of the people with the condition, but may also produce more false positives.
* Specificity refers to the proportion of people who do not have a particular condition (true negatives) who are correctly identified by the test. It is also known as the "true negative rate." A highly specific test will identify most or all of the people without the condition, but may also produce more false negatives.

In medical testing, both sensitivity and specificity are important considerations when evaluating a diagnostic test. High sensitivity is desirable for screening tests that aim to identify as many cases of a condition as possible, while high specificity is desirable for confirmatory tests that aim to rule out the condition in people who do not have it.

It's worth noting that sensitivity and specificity are often influenced by factors such as the prevalence of the condition in the population being tested, the threshold used to define a positive result, and the reliability and validity of the test itself. Therefore, it's important to consider these factors when interpreting the results of a diagnostic test.

Immune tolerance, also known as immunological tolerance or specific immune tolerance, is a state of unresponsiveness or non-reactivity of the immune system towards a particular substance (antigen) that has the potential to elicit an immune response. This occurs when the immune system learns to distinguish "self" from "non-self" and does not attack the body's own cells, tissues, and organs.

In the context of transplantation, immune tolerance refers to the absence of a destructive immune response towards the transplanted organ or tissue, allowing for long-term graft survival without the need for immunosuppressive therapy. Immune tolerance can be achieved through various strategies, including hematopoietic stem cell transplantation, costimulation blockade, and regulatory T cell induction.

In summary, immune tolerance is a critical mechanism that prevents the immune system from attacking the body's own structures while maintaining the ability to respond appropriately to foreign pathogens and antigens.

Cytotoxic T-lymphocytes, also known as CD8+ T cells, are a type of white blood cell that plays a central role in the cell-mediated immune system. They are responsible for identifying and destroying virus-infected cells and cancer cells. When a cytotoxic T-lymphocyte recognizes a specific antigen presented on the surface of an infected or malignant cell, it becomes activated and releases toxic substances such as perforins and granzymes, which can create pores in the target cell's membrane and induce apoptosis (programmed cell death). This process helps to eliminate the infected or malignant cells and prevent the spread of infection or cancer.

Echinostomiasis is a type of foodborne parasitic infection caused by eating raw or undercooked freshwater fish, snails, or aquatic plants contaminated with certain species of trematode flatworms in the family Echinostomatidae. These parasites have a complex life cycle involving several intermediate hosts, such as snails and fish, before they can infect humans.

Infection with echinostomes can cause various symptoms, including abdominal pain, diarrhea, nausea, vomiting, weight loss, and malnutrition. In severe cases, it may lead to liver damage or other complications. The diagnosis of echinostomiasis is usually made by identifying eggs or adult worms in the stool or through imaging techniques such as endoscopy.

Treatment for echinostomiasis typically involves administering anthelmintic drugs, such as praziquantel or albendazole, to kill the parasites. Preventive measures include cooking food thoroughly and avoiding the consumption of raw or undercooked freshwater fish, snails, or aquatic plants in areas where echinostomiasis is common.

Inbred strains of mice are defined as lines of mice that have been brother-sister mated for at least 20 consecutive generations. This results in a high degree of homozygosity, where the mice of an inbred strain are genetically identical to one another, with the exception of spontaneous mutations.

Inbred strains of mice are widely used in biomedical research due to their genetic uniformity and stability, which makes them useful for studying the genetic basis of various traits, diseases, and biological processes. They also provide a consistent and reproducible experimental system, as compared to outbred or genetically heterogeneous populations.

Some commonly used inbred strains of mice include C57BL/6J, BALB/cByJ, DBA/2J, and 129SvEv. Each strain has its own unique genetic background and phenotypic characteristics, which can influence the results of experiments. Therefore, it is important to choose the appropriate inbred strain for a given research question.

Hypersensitivity is an exaggerated or inappropriate immune response to a substance that is generally harmless to most people. It's also known as an allergic reaction. This abnormal response can be caused by various types of immunological mechanisms, including antibody-mediated reactions (types I, II, and III) and cell-mediated reactions (type IV). The severity of the hypersensitivity reaction can range from mild discomfort to life-threatening conditions. Common examples of hypersensitivity reactions include allergic rhinitis, asthma, atopic dermatitis, food allergies, and anaphylaxis.

"Schistosoma japonicum" is a species of parasitic flatworms (trematodes) that causes schistosomiasis, also known as snail fever, in humans. This disease is prevalent in East Asian countries such as China, Indonesia, and the Philippines.

The life cycle of Schistosoma japonicum involves freshwater snails as intermediate hosts. The parasites lay eggs in the blood vessels of the human host, which then pass through the body and are excreted into water. When the eggs hatch, they release miracidia that infect specific species of freshwater snails. After several developmental stages within the snail, the parasite releases cercariae, which can infect humans by penetrating the skin during contact with infested water.

Once inside the human host, the cercariae transform into schistosomula and migrate to the lungs, then to the liver, where they mature into adult worms. The adult worms pair up, mate, and produce eggs that can cause inflammation, granulomas, and fibrosis in various organs, depending on their location.

Schistosoma japonicum is responsible for significant morbidity and mortality in endemic areas, with symptoms ranging from fever, rash, and diarrhea to more severe complications such as liver damage, bladder cancer, and kidney failure. Preventive measures include avoiding contact with infested water, treating infected individuals, and improving sanitation and hygiene practices.

1. Receptors: In the context of physiology and medicine, receptors are specialized proteins found on the surface of cells or inside cells that detect and respond to specific molecules, known as ligands. Receptors play a crucial role in signal transduction, enabling cells to communicate with each other and respond to changes in their environment.
2. Antigen: An antigen is any substance (usually a protein) that can be recognized by the immune system and stimulate an immune response. Antigens can be foreign substances such as bacteria, viruses, or pollen, or they can be components of our own cells, such as tumor antigens in cancer cells. Antigens are typically bound and presented to the immune system by specialized cells called antigen-presenting cells (APCs).
3. T-Cell: T-cells, also known as T lymphocytes, are a type of white blood cell that plays a central role in cell-mediated immunity. T-cells are produced in the bone marrow and mature in the thymus gland. There are two main types of T-cells: CD4+ helper T-cells and CD8+ cytotoxic T-cells. Helper T-cells assist other immune cells, such as B-cells and macrophages, in mounting an immune response, while cytotoxic T-cells directly kill infected or cancerous cells.
4. Alpha-Beta: Alpha-beta is a type of T-cell receptor (TCR) that is found on the surface of most mature T-cells. The alpha-beta TCR is composed of two polypeptide chains, an alpha chain and a beta chain, that are held together by disulfide bonds. The alpha-beta TCR recognizes and binds to specific antigens presented in the context of major histocompatibility complex (MHC) molecules on the surface of APCs. This interaction is critical for initiating an immune response against infected or cancerous cells.

"Toxocara canis" is a species of roundworm that primarily infects canids, such as dogs and foxes. The adult worms live in the intestines of the host animal, where they lay eggs that are passed in the feces. These eggs can then mature and become infective to other animals, including humans, if they ingest them.

In humans, infection with "Toxocara canis" can cause a range of symptoms known as toxocariasis, which can include fever, coughing, wheezing, rash, and abdominal pain. In severe cases, the larvae of the worm can migrate to various organs in the body, including the eyes, leading to potentially serious complications.

Preventive measures for "Toxocara canis" infection include good hygiene practices, such as washing hands after handling pets or coming into contact with soil that may contain infected feces, and regular deworming of pets.

I believe there may be some confusion in your question. "Rabbits" is a common name used to refer to the Lagomorpha species, particularly members of the family Leporidae. They are small mammals known for their long ears, strong legs, and quick reproduction.

However, if you're referring to "rabbits" in a medical context, there is a term called "rabbit syndrome," which is a rare movement disorder characterized by repetitive, involuntary movements of the fingers, resembling those of a rabbit chewing. It is also known as "finger-chewing chorea." This condition is usually associated with certain medications, particularly antipsychotics, and typically resolves when the medication is stopped or adjusted.

Elephantiasis, filarial is a medical condition characterized by the severe swelling of limbs or other parts of the body due to the blockage of lymphatic vessels by parasitic worms. It is caused by infection with threadlike nematode filarial worms, such as Wuchereria bancrofti and Brugia timori. These worms are transmitted to humans through mosquito bites.

The blockage of lymphatic vessels leads to the accumulation of lymph fluid in the affected area, causing progressive swelling, thickening, and hardening of the skin and underlying tissues. In advanced cases, the skin may become rough, nodular, and fissured, resembling the hide of an elephant, hence the name "elephantiasis."

The condition is usually chronic and can cause significant disability and social stigma. While there is no cure for filarial elephantiasis, various treatments are available to alleviate symptoms, prevent transmission, and halt the progression of the disease. These include antibiotics to kill the worms, surgery to remove the lymphatic obstruction, and various supportive measures to manage the swelling and prevent secondary infections.

Ivermectin is an anti-parasitic drug that is used to treat a variety of infections caused by parasites such as roundworms, threadworms, and lice. It works by paralyzing and killing the parasites, thereby eliminating the infection. Ivermectin is available in various forms, including tablets, creams, and solutions for topical use, as well as injections for veterinary use.

Ivermectin has been shown to be effective against a wide range of parasitic infections, including onchocerciasis (river blindness), strongyloidiasis, scabies, and lice infestations. It is also being studied as a potential treatment for other conditions, such as COVID-19, although its effectiveness for this use has not been proven.

Ivermectin is generally considered safe when used as directed, but it can cause side effects in some people, including skin rashes, nausea, and diarrhea. It should be used with caution in pregnant women and people with certain medical conditions, such as liver or kidney disease.

Antibodies, viral are proteins produced by the immune system in response to an infection with a virus. These antibodies are capable of recognizing and binding to specific antigens on the surface of the virus, which helps to neutralize or destroy the virus and prevent its replication. Once produced, these antibodies can provide immunity against future infections with the same virus.

Viral antibodies are typically composed of four polypeptide chains - two heavy chains and two light chains - that are held together by disulfide bonds. The binding site for the antigen is located at the tip of the Y-shaped structure, formed by the variable regions of the heavy and light chains.

There are five classes of antibodies in humans: IgA, IgD, IgE, IgG, and IgM. Each class has a different function and is distributed differently throughout the body. For example, IgG is the most common type of antibody found in the bloodstream and provides long-term immunity against viruses, while IgA is found primarily in mucous membranes and helps to protect against respiratory and gastrointestinal infections.

In addition to their role in the immune response, viral antibodies can also be used as diagnostic tools to detect the presence of a specific virus in a patient's blood or other bodily fluids.

Immunoelectrophoresis (IEP) is a laboratory technique used in the field of clinical pathology and immunology. It is a method for separating and identifying proteins, particularly immunoglobulins or antibodies, in a sample. This technique combines the principles of electrophoresis, which separates proteins based on their electric charge and size, with immunological reactions, which detect specific proteins using antigen-antibody interactions.

In IEP, a protein sample is first separated by electrophoresis in an agarose or agar gel matrix on a glass slide or in a test tube. After separation, an antibody specific to the protein of interest is layered on top of the gel and allowed to diffuse towards the separated proteins. This creates a reaction between the antigen (protein) and the antibody, forming a visible precipitate at the point where they meet. The precipitate line's position and intensity can then be analyzed to identify and quantify the protein of interest.

Immunoelectrophoresis is particularly useful in diagnosing various medical conditions, such as immunodeficiency disorders, monoclonal gammopathies (like multiple myeloma), and other plasma cell dyscrasias. It can help detect abnormal protein patterns, quantify specific immunoglobulins, and identify the presence of M-proteins or Bence Jones proteins, which are indicative of monoclonal gammopathies.

Parasitic diseases, animal, refer to conditions in animals that are caused by parasites, which are organisms that live on or inside a host and derive benefits from the host at its expense. Parasites can be classified into different groups such as protozoa, helminths (worms), and arthropods (e.g., ticks, fleas).

Parasitic diseases in animals can cause a wide range of clinical signs depending on the type of parasite, the animal species affected, and the location and extent of infection. Some common examples of parasitic diseases in animals include:

* Heartworm disease in dogs and cats caused by Dirofilaria immitis
* Coccidiosis in various animals caused by different species of Eimeria
* Toxoplasmosis in cats and other animals caused by Toxoplasma gondii
* Giardiasis in many animal species caused by Giardia spp.
* Lungworm disease in dogs and cats caused by Angiostrongylus vasorum or Aelurostrongylus abstrusus
* Tapeworm infection in dogs, cats, and other animals caused by different species of Taenia or Dipylidium caninum

Prevention and control of parasitic diseases in animals typically involve a combination of strategies such as regular veterinary care, appropriate use of medications, environmental management, and good hygiene practices.

CTLA-4 (Cytotoxic T-Lymphocyte Associated Protein 4) antigen is a type of protein found on the surface of activated T cells, which are a type of white blood cell in the immune system. CTLA-4 plays an important role in regulating the immune response by functioning as a negative regulator of T cell activation.

CTLA-4 binds to CD80 and CD86 molecules on the surface of antigen-presenting cells, which are cells that display foreign antigens to T cells and activate them. By binding to these molecules, CTLA-4 inhibits T cell activation and helps prevent an overactive immune response.

CTLA-4 is a target for cancer immunotherapy because blocking its function can enhance the anti-tumor immune response. Certain drugs called checkpoint inhibitors work by blocking CTLA-4, allowing T cells to remain active and attack tumor cells more effectively.

CD8-positive T-lymphocytes, also known as CD8+ T cells or cytotoxic T cells, are a type of white blood cell that plays a crucial role in the adaptive immune system. They are named after the CD8 molecule found on their surface, which is a protein involved in cell signaling and recognition.

CD8+ T cells are primarily responsible for identifying and destroying virus-infected cells or cancerous cells. When activated, they release cytotoxic granules that contain enzymes capable of inducing apoptosis (programmed cell death) in the target cells. They also produce cytokines such as interferon-gamma, which can help coordinate the immune response and activate other immune cells.

CD8+ T cells are generated in the thymus gland and are a type of T cell, which is a lymphocyte that matures in the thymus and plays a central role in cell-mediated immunity. They recognize and respond to specific antigens presented on the surface of infected or cancerous cells in conjunction with major histocompatibility complex (MHC) class I molecules.

Overall, CD8+ T cells are an essential component of the immune system's defense against viral infections and cancer.

Antinematodal agents are a type of medication used to treat infections caused by nematodes, which are also known as roundworms. These agents work by either killing the parasitic worms or preventing them from reproducing. Some examples of antinematodal agents include albendazole, ivermectin, and mebendazole. These medications are used to treat a variety of nematode infections, such as ascariasis, hookworm infection, and strongyloidiasis. It is important to note that the use of antinematodal agents should be under the guidance of a healthcare professional, as they can have side effects and may interact with other medications.

Hygiene is the science and practice of maintaining and promoting health and preventing disease through cleanliness in personal and public environments. It includes various measures such as handwashing, bathing, using clean clothes, cleaning and disinfecting surfaces, proper waste disposal, safe food handling, and managing water supplies to prevent the spread of infectious agents like bacteria, viruses, and parasites.

In a medical context, hygiene is crucial in healthcare settings to prevent healthcare-associated infections (HAIs) and ensure patient safety. Healthcare professionals are trained in infection control practices, including proper hand hygiene, use of personal protective equipment (PPE), environmental cleaning and disinfection, and safe injection practices.

Overall, maintaining good hygiene is essential for overall health and well-being, reducing the risk of illness and promoting a healthy lifestyle.

Amoebozoa is a supergroup of unicellular eukaryotic organisms that includes various kinds of amoebas and slime molds. These organisms are characterized by the presence of lobose pseudopodia, which are temporary protrusions of cytoplasm used for locomotion and feeding. Amoebozoa is a diverse group with over 9,000 described species, including both free-living and symbiotic forms. Some amoebozoans can form multicellular structures during their life cycle, such as slime molds, which are known for their complex behaviors and social interactions. The study of Amoebozoa is important for understanding the evolutionary history and diversity of eukaryotic organisms.

Onchocerciasis is a neglected tropical disease caused by the parasitic worm Onchocerca volvulus. The infection is primarily transmitted through the bites of infected blackflies (Simulium spp.) that breed in fast-flowing rivers and streams. The larvae of the worms mature into adults in nodules under the skin, where females release microfilariae that migrate throughout the body, including the eyes.

Symptoms include severe itching, dermatitis, depigmentation, thickening and scarring of the skin, visual impairment, and blindness. The disease is also known as river blindness due to its association with riverside communities where blackflies breed. Onchocerciasis can lead to significant social and economic consequences for affected individuals and communities. Preventive chemotherapy using mass drug administration of ivermectin is the primary strategy for controlling onchocerciasis in endemic areas.

Neglected Tropical Diseases (NTDs) are a group of infectious diseases that primarily affect people living in poverty, in tropical and subtropical areas. These diseases are called "neglected" because they have been largely ignored by medical research and drug development, as well as by global health agencies and pharmaceutical companies.

The World Health Organization (WHO) has identified 20 diseases as NTDs, including:

1. Buruli ulcer
2. Chagas disease
3. Dengue and chikungunya
4. Dracunculiasis (guinea-worm disease)
5. Echinococcosis
6. Endemic treponematoses
7. Foodborne trematodiases
8. Human African trypanosomiasis (sleeping sickness)
9. Leishmaniasis
10. Leprosy (Hansen's disease)
11. Lymphatic filariasis
12. Onchocerciasis (river blindness)
13. Rabies
14. Schistosomiasis
15. Soil-transmitted helminthiases
16. Snakebite envenoming
17. Taeniasis/Cysticercosis
18. Trachoma
19. Mycetoma, chromoblastomycosis and other deep mycoses
20. Yaws (Endemic treponematoses)

These diseases can lead to severe disfigurement, disability, and even death if left untreated. They affect more than 1 billion people worldwide, mainly in low-income countries in Africa, Asia, and the Americas. NTDs also have significant social and economic impacts, contributing to poverty, stigma, discrimination, and exclusion.

Efforts are underway to raise awareness and increase funding for research, prevention, and treatment of NTDs. The WHO has set targets for controlling or eliminating several NTDs by 2030, including dracunculiasis, lymphatic filariasis, onchocerciasis, trachoma, and human African trypanosomiasis.

CD79 is a type of protein that is found on the surface of B cells, which are a type of white blood cell that plays a key role in the immune system. CD79 combines with another protein called CD19 to form a complex that helps to activate B cells and initiate an immune response when the body encounters an antigen.

An antigen is any substance that can stimulate an immune response, particularly the production of antibodies. Antigens can be proteins, polysaccharides, or other molecules found on the surface of viruses, bacteria, or other foreign substances. When a B cell encounters an antigen, it engulfs and processes the antigen, then displays a portion of it on its surface along with CD79 and CD19. This helps to activate the B cell and stimulate it to divide and differentiate into plasma cells, which produce and secrete large amounts of antibodies that recognize and bind to the antigen.

CD79 is an important marker for identifying and studying B cells, and it has been implicated in various B-cell malignancies such as chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma (NHL).

Antibodies, protozoan, refer to the immune system's response to an infection caused by a protozoan organism. Protozoa are single-celled microorganisms that can cause various diseases in humans, such as malaria, giardiasis, and toxoplasmosis.

When the body is infected with a protozoan, the immune system responds by producing specific proteins called antibodies. Antibodies are produced by a type of white blood cell called a B-cell, and they recognize and bind to specific antigens on the surface of the protozoan organism.

There are five main types of antibodies: IgA, IgD, IgE, IgG, and IgM. Each type of antibody has a different role in the immune response. For example, IgG is the most common type of antibody and provides long-term immunity to previously encountered pathogens. IgM is the first antibody produced in response to an infection and is important for activating the complement system, which helps to destroy the protozoan organism.

Overall, the production of antibodies against protozoan organisms is a critical part of the immune response and helps to protect the body from further infection.

Lymph nodes are small, bean-shaped organs that are part of the immune system. They are found throughout the body, especially in the neck, armpits, groin, and abdomen. Lymph nodes filter lymph fluid, which carries waste and unwanted substances such as bacteria, viruses, and cancer cells. They contain white blood cells called lymphocytes that help fight infections and diseases by attacking and destroying the harmful substances found in the lymph fluid. When an infection or disease is present, lymph nodes may swell due to the increased number of immune cells and fluid accumulation as they work to fight off the invaders.

CA 19-9 antigen, also known as carbohydrate antigen 19-9, is a tumor marker that is commonly found in the blood. It is a type of sialylated Lewis blood group antigen, which is a complex carbohydrate molecule found on the surface of many cells in the body.

CA 19-9 antigen is often elevated in people with certain types of cancer, particularly pancreatic cancer, bile duct cancer, and colon cancer. However, it can also be elevated in noncancerous conditions such as pancreatitis, liver cirrhosis, and cholestasis. Therefore, CA 19-9 antigen is not a specific or sensitive marker for cancer, and its use as a screening test for cancer is not recommended.

Instead, CA 19-9 antigen is often used as a tumor marker to monitor the response to treatment in people with known cancers, particularly pancreatic cancer. A decrease in CA 19-9 antigen levels may indicate that the cancer is responding to treatment, while an increase may suggest that the cancer is growing or has recurred. However, it is important to note that CA 19-9 antigen levels can also be affected by other factors, such as the size and location of the tumor, the presence of obstructive jaundice, and the patient's overall health status. Therefore, CA 19-9 antigen should always be interpreted in conjunction with other clinical and diagnostic findings.

A "knockout" mouse is a genetically engineered mouse in which one or more genes have been deleted or "knocked out" using molecular biology techniques. This allows researchers to study the function of specific genes and their role in various biological processes, as well as potential associations with human diseases. The mice are generated by introducing targeted DNA modifications into embryonic stem cells, which are then used to create a live animal. Knockout mice have been widely used in biomedical research to investigate gene function, disease mechanisms, and potential therapeutic targets.

Ancylostomiasis is a parasitic infection caused by the hookworms, Ancylostoma duodenale and Necator americanus. These tiny worms infect the human intestines, specifically in the small intestine, where they attach themselves to the intestinal wall and feed on the host's blood.

The infection is typically acquired through skin contact with contaminated soil, particularly in areas where human feces are used as fertilizer or where there is poor sanitation. The larvae penetrate the skin, enter the bloodstream, and migrate to the lungs, where they mature further before being coughed up and swallowed, eventually reaching the small intestine.

Symptoms of ancylostomiasis can range from mild to severe and may include abdominal pain, diarrhea, anemia, weight loss, and fatigue. In severe cases, particularly in children or individuals with weakened immune systems, the infection can lead to protein-energy malnutrition, cognitive impairment, and even death.

Treatment for ancylostomiasis typically involves administration of anthelmintic medications such as albendazole or mebendazole, which kill the parasitic worms. Improved sanitation and hygiene practices can help prevent reinfection and reduce the spread of the disease.

Transgenic mice are genetically modified rodents that have incorporated foreign DNA (exogenous DNA) into their own genome. This is typically done through the use of recombinant DNA technology, where a specific gene or genetic sequence of interest is isolated and then introduced into the mouse embryo. The resulting transgenic mice can then express the protein encoded by the foreign gene, allowing researchers to study its function in a living organism.

The process of creating transgenic mice usually involves microinjecting the exogenous DNA into the pronucleus of a fertilized egg, which is then implanted into a surrogate mother. The offspring that result from this procedure are screened for the presence of the foreign DNA, and those that carry the desired genetic modification are used to establish a transgenic mouse line.

Transgenic mice have been widely used in biomedical research to model human diseases, study gene function, and test new therapies. They provide a valuable tool for understanding complex biological processes and developing new treatments for a variety of medical conditions.

Parasitic pregnancy complications refer to a rare condition where a parasitic twin takes over the development of the dominant twin's reproductive system and becomes pregnant. This condition is also known as fetus in fetu or vanishing twin syndrome with a parasitic twin. The parasitic twin may have some organs developed, but it is not fully formed and relies on the dominant twin for survival. The pregnancy can pose risks to the dominant twin, such as abnormal growth patterns, organ damage, and complications during childbirth. This condition is usually detected during prenatal ultrasound examinations.

Th1 cells, or Type 1 T helper cells, are a subset of CD4+ T cells that play a crucial role in the cell-mediated immune response. They are characterized by the production of specific cytokines, such as interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), and interleukin-2 (IL-2). Th1 cells are essential for protecting against intracellular pathogens, including viruses, bacteria, and parasites. They activate macrophages to destroy ingested microorganisms, stimulate the differentiation of B cells into plasma cells that produce antibodies, and recruit other immune cells to the site of infection. Dysregulation of Th1 cell responses has been implicated in various autoimmune diseases, such as multiple sclerosis, rheumatoid arthritis, and type 1 diabetes.

Hemagglutination tests are laboratory procedures used to detect the presence of antibodies or antigens in a sample, typically in blood serum. These tests rely on the ability of certain substances, such as viruses or bacteria, to agglutinate (clump together) red blood cells.

In a hemagglutination test, a small amount of the patient's serum is mixed with a known quantity of red blood cells that have been treated with a specific antigen. If the patient has antibodies against that antigen in their serum, they will bind to the antigens on the red blood cells and cause them to agglutinate. This clumping can be observed visually, indicating a positive test result.

Hemagglutination tests are commonly used to diagnose infectious diseases caused by viruses or bacteria that have hemagglutinating properties, such as influenza, parainfluenza, and HIV. They can also be used in blood typing and cross-matching before transfusions.

The gp100 melanoma antigen, also known as Pmel17 or gp100, is a protein found on the surface of melanocytes, which are the pigment-producing cells in the skin. It is overexpressed in melanoma cells and can be recognized by the immune system as a foreign target, making it an attractive candidate for cancer immunotherapy. The gp100 protein plays a role in the formation and transport of melanosomes, which are organelles involved in the production and distribution of melanin. In melanoma, mutations or abnormal regulation of gp100 can contribute to uncontrolled cell growth and survival, leading to the development of cancer. The gp100 protein is used as a target for various immunotherapeutic approaches, such as vaccines and monoclonal antibodies, to stimulate an immune response against melanoma cells.

Serologic tests are laboratory tests that detect the presence or absence of antibodies or antigens in a patient's serum (the clear liquid that separates from clotted blood). These tests are commonly used to diagnose infectious diseases, as well as autoimmune disorders and other medical conditions.

In serologic testing for infectious diseases, a sample of the patient's blood is collected and allowed to clot. The serum is then separated from the clot and tested for the presence of antibodies that the body has produced in response to an infection. The test may be used to identify the specific type of infection or to determine whether the infection is active or has resolved.

Serologic tests can also be used to diagnose autoimmune disorders, such as rheumatoid arthritis and lupus, by detecting the presence of antibodies that are directed against the body's own tissues. These tests can help doctors confirm a diagnosis and monitor the progression of the disease.

It is important to note that serologic tests are not always 100% accurate and may produce false positive or false negative results. Therefore, they should be interpreted in conjunction with other clinical findings and laboratory test results.

The Lewis blood-group system is one of the human blood group systems, which is based on the presence or absence of two antigens: Lea and Leb. These antigens are carbohydrate structures that can be found on the surface of red blood cells (RBCs) as well as other cells and in various body fluids.

The Lewis system is unique because its antigens are not normally present at birth, but instead develop during early childhood or later in life due to the action of certain enzymes in the digestive tract. The production of Lea and Leb antigens depends on the activity of two genes, FUT3 (also known as Lewis gene) and FUT2 (also known as Secretor gene).

There are four main phenotypes or blood types in the Lewis system:

1. Le(a+b-): This is the most common phenotype, where individuals have both Lea and Leb antigens on their RBCs.
2. Le(a-b+): In this phenotype, individuals lack the Lea antigen but have the Leb antigen on their RBCs.
3. Le(a-b-): This is a rare phenotype where neither Lea nor Leb antigens are present on the RBCs.
4. Le(a+b+): In this phenotype, individuals have both Lea and Leb antigens on their RBCs due to the simultaneous expression of FUT3 and FUT2 genes.

The Lewis blood-group system is not typically associated with transfusion reactions or hemolytic diseases, unlike other blood group systems such as ABO and Rh. However, the presence or absence of Lewis antigens can still have implications for certain medical conditions and tests, including:

* Infectious diseases: Some bacteria and viruses can use the Lewis antigens as receptors to attach to and infect host cells. For example, Helicobacter pylori, which causes gastritis and peptic ulcers, binds to Lea antigens in the stomach.
* Autoimmune disorders: In some cases, autoantibodies against Lewis antigens have been found in patients with autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus (SLE).
* Pregnancy: The Lewis antigens can be expressed on the surface of placental cells, and changes in their expression have been linked to pregnancy complications such as preeclampsia and fetal growth restriction.
* Blood typing: Although not a primary factor in blood transfusion compatibility, the Lewis blood-group system is still considered when determining the best match for patients who require frequent transfusions or organ transplants.

I'm sorry for any confusion, but "Laos" is not a medical term. It is the name of a country, the Lao People's Democratic Republic, located in Southeast Asia. If you have any questions about medical terms or health-related topics, I'd be happy to try and help answer them!

The Ki-67 antigen is a cellular protein that is expressed in all active phases of the cell cycle (G1, S, G2, and M), but not in the resting phase (G0). It is often used as a marker for cell proliferation and can be found in high concentrations in rapidly dividing cells. Immunohistochemical staining for Ki-67 can help to determine the growth fraction of a group of cells, which can be useful in the diagnosis and prognosis of various malignancies, including cancer. The level of Ki-67 expression is often associated with the aggressiveness of the tumor and its response to treatment.

Tropical medicine is a branch of medicine that deals with health problems that are prevalent in or unique to tropical and subtropical regions. These regions are typically characterized by hot and humid climates, and often have distinct ecological systems that can contribute to the spread of infectious diseases.

The field of tropical medicine encompasses a wide range of health issues, including:

1. Infectious diseases: Many tropical diseases are caused by infectious agents such as bacteria, viruses, parasites, and fungi. Some of the most common infectious diseases in the tropics include malaria, dengue fever, yellow fever, chikungunya, Zika virus, leishmaniasis, schistosomiasis, and Chagas disease.
2. Neglected tropical diseases (NTDs): A group of chronic infectious diseases that primarily affect poor and marginalized populations in the tropics. NTDs include diseases such as human African trypanosomiasis (sleeping sickness), leprosy, Buruli ulcer, and dracunculiasis (guinea worm disease).
3. Zoonotic diseases: Diseases that are transmitted between animals and humans, often through insect vectors or contaminated food and water. Examples of zoonotic diseases in the tropics include rabies, leptospirosis, and Rift Valley fever.
4. Environmental health issues: The tropical environment can pose unique health challenges, such as exposure to toxic chemicals, heat stress, and poor air quality. Tropical medicine also addresses these environmental health issues.
5. Travel medicine: As global travel increases, there is a growing need for medical professionals who are knowledgeable about the health risks associated with traveling to tropical destinations. Tropical medicine physicians often provide pre-travel consultations and post-travel evaluations for international travelers.

Overall, tropical medicine is an essential field that addresses the unique health challenges faced by populations living in or traveling to tropical and subtropical regions.

Interleukin-10 (IL-10) is an anti-inflammatory cytokine that plays a crucial role in the modulation of immune responses. It is produced by various cell types, including T cells, macrophages, and dendritic cells. IL-10 inhibits the production of pro-inflammatory cytokines, such as TNF-α, IL-1, IL-6, IL-8, and IL-12, and downregulates the expression of costimulatory molecules on antigen-presenting cells. This results in the suppression of T cell activation and effector functions, which ultimately helps to limit tissue damage during inflammation and promote tissue repair. Dysregulation of IL-10 has been implicated in various pathological conditions, including chronic infections, autoimmune diseases, and cancer.

Oxyurida is an order of nematode worms, also known as pinworms or threadworms. The most well-known species in this group is Enterobius vermicularis, which is a common parasite in humans. Oxyurids are small, white, and thread-like in appearance, and they typically infect the gastrointestinal tract of their hosts.

Infection with Oxyurida occurs when individuals accidentally ingest the eggs of these worms, often through contaminated food or drink. Once inside the body, the larvae hatch from the eggs and migrate to the large intestine, where they mature into adult worms. Female adults then lay their eggs around the anus, typically at night, which can cause intense itching and discomfort.

Oxyurida infections are most commonly seen in children, but they can also occur in adults who have close contact with infected individuals or engage in poor hygiene practices. Treatment for Oxyurida infections typically involves the use of anti-parasitic medications to kill the worms and prevent their eggs from hatching. Good hygiene practices, such as washing hands frequently and avoiding nail-biting, can also help prevent the spread of these parasites.

Species specificity is a term used in the field of biology, including medicine, to refer to the characteristic of a biological entity (such as a virus, bacterium, or other microorganism) that allows it to interact exclusively or preferentially with a particular species. This means that the biological entity has a strong affinity for, or is only able to infect, a specific host species.

For example, HIV is specifically adapted to infect human cells and does not typically infect other animal species. Similarly, some bacterial toxins are species-specific and can only affect certain types of animals or humans. This concept is important in understanding the transmission dynamics and host range of various pathogens, as well as in developing targeted therapies and vaccines.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

Macrophages are a type of white blood cell that are an essential part of the immune system. They are large, specialized cells that engulf and destroy foreign substances, such as bacteria, viruses, parasites, and fungi, as well as damaged or dead cells. Macrophages are found throughout the body, including in the bloodstream, lymph nodes, spleen, liver, lungs, and connective tissues. They play a critical role in inflammation, immune response, and tissue repair and remodeling.

Macrophages originate from monocytes, which are a type of white blood cell produced in the bone marrow. When monocytes enter the tissues, they differentiate into macrophages, which have a larger size and more specialized functions than monocytes. Macrophages can change their shape and move through tissues to reach sites of infection or injury. They also produce cytokines, chemokines, and other signaling molecules that help coordinate the immune response and recruit other immune cells to the site of infection or injury.

Macrophages have a variety of surface receptors that allow them to recognize and respond to different types of foreign substances and signals from other cells. They can engulf and digest foreign particles, bacteria, and viruses through a process called phagocytosis. Macrophages also play a role in presenting antigens to T cells, which are another type of immune cell that helps coordinate the immune response.

Overall, macrophages are crucial for maintaining tissue homeostasis, defending against infection, and promoting wound healing and tissue repair. Dysregulation of macrophage function has been implicated in a variety of diseases, including cancer, autoimmune disorders, and chronic inflammatory conditions.

Membrane glycoproteins are proteins that contain oligosaccharide chains (glycans) covalently attached to their polypeptide backbone. They are integral components of biological membranes, spanning the lipid bilayer and playing crucial roles in various cellular processes.

The glycosylation of these proteins occurs in the endoplasmic reticulum (ER) and Golgi apparatus during protein folding and trafficking. The attached glycans can vary in structure, length, and composition, which contributes to the diversity of membrane glycoproteins.

Membrane glycoproteins can be classified into two main types based on their orientation within the lipid bilayer:

1. Type I (N-linked): These glycoproteins have a single transmembrane domain and an extracellular N-terminus, where the oligosaccharides are predominantly attached via asparagine residues (Asn-X-Ser/Thr sequon).
2. Type II (C-linked): These glycoproteins possess two transmembrane domains and an intracellular C-terminus, with the oligosaccharides linked to tryptophan residues via a mannose moiety.

Membrane glycoproteins are involved in various cellular functions, such as:

* Cell adhesion and recognition
* Receptor-mediated signal transduction
* Enzymatic catalysis
* Transport of molecules across membranes
* Cell-cell communication
* Immunological responses

Some examples of membrane glycoproteins include cell surface receptors (e.g., growth factor receptors, cytokine receptors), adhesion molecules (e.g., integrins, cadherins), and transporters (e.g., ion channels, ABC transporters).

T-independent antigens are types of antigens that can stimulate an immune response without the help of T cells. They are typically small molecules with repetitive structures, such as polysaccharides found on bacterial cell walls, that can directly activate B cells through their surface receptors. This results in the production of antibodies specific to the antigen, but it does not lead to the development of immunological memory. Therefore, immunity to T-independent antigens is usually short-lived and provides limited protection against future infections.

CD2 is a type of cell surface protein known as a glycoprotein that is found on the surface of T cells, natural killer (NK) cells, and thymocytes in humans. It plays a role in the activation and regulation of the immune response. CD2 can also function as an adhesion molecule, helping to bind T cells to other cells during an immune response.

An antigen is any substance that can stimulate an immune response, leading to the production of antibodies or the activation of immune cells such as T cells. In the context of CD2, an "antigen" may refer to a specific molecule or structure that interacts with CD2 and triggers a response from T cells or other immune cells.

It's worth noting that while CD2 can interact with certain antigens, it is not itself an antigen in the traditional sense. However, the term "antigen" is sometimes used more broadly to refer to any molecule that interacts with the immune system and triggers a response, so it is possible for CD2 to be referred to as an "antigen" in this context.

Hepatitis B e antigen (HBeAg) is a protein produced by the hepatitis B virus (HBV) during its replication process. It can be found in the blood of individuals infected with HBV. The presence of HBeAg generally indicates that the virus is actively replicating in the liver and that the individual has high levels of viral load.

HBeAg is a serological marker used to assess the severity and activity of HBV infection, as well as the response to antiviral treatment. In particular, the disappearance of HBeAg from the blood (known as seroconversion) is often associated with a decrease in viral replication and an improvement in liver disease. However, the presence of HBeAg does not necessarily mean that the individual will develop symptoms or liver damage, as some people can remain asymptomatic carriers of the virus for many years.

It's important to note that not all HBV strains produce HBeAg, and some mutant strains may not produce detectable levels of this antigen even when the virus is actively replicating. Therefore, additional tests may be needed to confirm the presence or absence of HBV infection in these cases.

'Brugia' is a genus of parasitic nematode worms that are known to cause lymphatic filariasis, a tropical disease affecting the lymphatic system. There are three main species of Brugia that infect humans: Brugia malayi, Brugia timori, and Brugia garinii. These parasites are transmitted to humans through the bite of infected mosquitoes.

Brugia malayi is found primarily in Southeast Asia, while Brugia timori is restricted to the island of Timor in Indonesia. Brugia garinii, on the other hand, is more widely distributed and can be found in parts of Africa and Asia.

The infection caused by these parasites can lead to a range of symptoms, including fever, swelling of the lymph nodes, and elephantiasis, a condition characterized by severe swelling of the limbs or genitals. Preventive measures such as avoiding mosquito bites and mass drug administration programs are in place to control the spread of lymphatic filariasis caused by Brugia species.

Methyl Green is not typically considered a medical term, but it is a chemical compound that has been used in various medical and laboratory contexts. Here's the general definition:

Methyl Green is a basic dye, which is a type of organic compound with positively charged ions (cations). It is commonly used as a biological stain to selectively color certain structures in cells or tissues, such as nucleic acids (DNA and RNA), during microscopic examination.

In the medical field, Methyl Green has been used as a component of some topical ointments for treating superficial bacterial infections. However, its use is not widespread due to the availability of more effective antibiotics.

It's important to note that Methyl Green should not be confused with Methylene Blue, another basic dye that has broader medical applications, such as treating methemoglobinemia and used as a marker in some diagnostic tests.

Electrophoresis, polyacrylamide gel (EPG) is a laboratory technique used to separate and analyze complex mixtures of proteins or nucleic acids (DNA or RNA) based on their size and electrical charge. This technique utilizes a matrix made of cross-linked polyacrylamide, a type of gel, which provides a stable and uniform environment for the separation of molecules.

In this process:

1. The polyacrylamide gel is prepared by mixing acrylamide monomers with a cross-linking agent (bis-acrylamide) and a catalyst (ammonium persulfate) in the presence of a buffer solution.
2. The gel is then poured into a mold and allowed to polymerize, forming a solid matrix with uniform pore sizes that depend on the concentration of acrylamide used. Higher concentrations result in smaller pores, providing better resolution for separating smaller molecules.
3. Once the gel has set, it is placed in an electrophoresis apparatus containing a buffer solution. Samples containing the mixture of proteins or nucleic acids are loaded into wells on the top of the gel.
4. An electric field is applied across the gel, causing the negatively charged molecules to migrate towards the positive electrode (anode) while positively charged molecules move toward the negative electrode (cathode). The rate of migration depends on the size, charge, and shape of the molecules.
5. Smaller molecules move faster through the gel matrix and will migrate farther from the origin compared to larger molecules, resulting in separation based on size. Proteins and nucleic acids can be selectively stained after electrophoresis to visualize the separated bands.

EPG is widely used in various research fields, including molecular biology, genetics, proteomics, and forensic science, for applications such as protein characterization, DNA fragment analysis, cloning, mutation detection, and quality control of nucleic acid or protein samples.

Vaccination is a simple, safe, and effective way to protect people against harmful diseases, before they come into contact with them. It uses your body's natural defenses to build protection to specific infections and makes your immune system stronger.

A vaccination usually contains a small, harmless piece of a virus or bacteria (or toxins produced by these germs) that has been made inactive or weakened so it won't cause the disease itself. This piece of the germ is known as an antigen. When the vaccine is introduced into the body, the immune system recognizes the antigen as foreign and produces antibodies to fight it.

If a person then comes into contact with the actual disease-causing germ, their immune system will recognize it and immediately produce antibodies to destroy it. The person is therefore protected against that disease. This is known as active immunity.

Vaccinations are important for both individual and public health. They prevent the spread of contagious diseases and protect vulnerable members of the population, such as young children, the elderly, and people with weakened immune systems who cannot be vaccinated or for whom vaccination is not effective.

Immunologic adjuvants are substances that are added to a vaccine to enhance the body's immune response to the antigens contained in the vaccine. They work by stimulating the immune system and promoting the production of antibodies and activating immune cells, such as T-cells and macrophages, which help to provide a stronger and more sustained immune response to the vaccine.

Immunologic adjuvants can be derived from various sources, including bacteria, viruses, and chemicals. Some common examples include aluminum salts (alum), oil-in-water emulsions (such as MF59), and bacterial components (such as lipopolysaccharide or LPS).

The use of immunologic adjuvants in vaccines can help to improve the efficacy of the vaccine, particularly for vaccines that contain weak or poorly immunogenic antigens. They can also help to reduce the amount of antigen needed in a vaccine, which can be beneficial for vaccines that are difficult or expensive to produce.

It's important to note that while adjuvants can enhance the immune response to a vaccine, they can also increase the risk of adverse reactions, such as inflammation and pain at the injection site. Therefore, the use of immunologic adjuvants must be carefully balanced against their potential benefits and risks.

I'm sorry for any confusion, but "hydrology" is not a term typically used in medical definitions. Hydrology is the scientific study of the movement, distribution, and quality of water on Earth and other planets, including the hydrologic cycle, water resources and environmental impacts of water usage.

However, if you meant to ask about "hemodynamics" or "hydrostatic equilibrium," these are medical terms related to fluid dynamics within the body:

1. Hemodynamics: This term refers to the study of blood flow or the circulation of blood in the body, including the forces involved (such as pressure and resistance) and the properties of the blood vessels. It is a crucial aspect of understanding cardiovascular function and disease.
2. Hydrostatic equilibrium: In medical terms, this concept relates to the balance between the forces exerted by fluids within the body, particularly in reference to the distribution of body fluids and the maintenance of fluid compartments (intracellular and extracellular). It is essential for maintaining proper physiological functioning.

Please let me know if you had a different term or concept in mind, and I would be happy to help further!

Delayed hypersensitivity, also known as type IV hypersensitivity, is a type of immune response that takes place several hours to days after exposure to an antigen. It is characterized by the activation of T cells (a type of white blood cell) and the release of various chemical mediators, leading to inflammation and tissue damage. This reaction is typically associated with chronic inflammatory diseases, such as contact dermatitis, granulomatous disorders (e.g. tuberculosis), and certain autoimmune diseases.

The reaction process involves the following steps:

1. Sensitization: The first time an individual is exposed to an antigen, T cells are activated and become sensitized to it. This process can take several days.
2. Memory: Some of the activated T cells differentiate into memory T cells, which remain in the body and are ready to respond quickly if the same antigen is encountered again.
3. Effector phase: Upon subsequent exposure to the antigen, the memory T cells become activated and release cytokines, which recruit other immune cells (e.g. macrophages) to the site of inflammation. These cells cause tissue damage through various mechanisms, such as phagocytosis, degranulation, and the release of reactive oxygen species.
4. Chronic inflammation: The ongoing immune response can lead to chronic inflammation, which may result in tissue destruction and fibrosis (scarring).

Examples of conditions associated with delayed hypersensitivity include:

* Contact dermatitis (e.g. poison ivy, nickel allergy)
* Tuberculosis
* Leprosy
* Sarcoidosis
* Rheumatoid arthritis
* Type 1 diabetes mellitus
* Multiple sclerosis
* Inflammatory bowel disease (e.g. Crohn's disease, ulcerative colitis)

Immunologic cytotoxicity refers to the damage or destruction of cells that occurs as a result of an immune response. This process involves the activation of immune cells, such as cytotoxic T cells and natural killer (NK) cells, which release toxic substances, such as perforins and granzymes, that can kill target cells.

In addition, antibodies produced by B cells can also contribute to immunologic cytotoxicity by binding to antigens on the surface of target cells and triggering complement-mediated lysis or antibody-dependent cellular cytotoxicity (ADCC) by activating immune effector cells.

Immunologic cytotoxicity plays an important role in the body's defense against viral infections, cancer cells, and other foreign substances. However, it can also contribute to tissue damage and autoimmune diseases if the immune system mistakenly targets healthy cells or tissues.

CD28 is a co-stimulatory molecule that plays an important role in the activation and regulation of T cells, which are key players in the immune response. It is a type of protein found on the surface of T cells and interacts with other proteins called B7-1 (also known as CD80) and B7-2 (also known as CD86) that are expressed on the surface of antigen-presenting cells (APCs).

When a T cell encounters an APC that is presenting an antigen, the T cell receptor (TCR) on the surface of the T cell recognizes and binds to the antigen. However, this interaction alone is not enough to fully activate the T cell. The engagement of CD28 with B7-1 or B7-2 provides a critical co-stimulatory signal that promotes T cell activation, proliferation, and survival.

CD28 is also an important target for immune checkpoint inhibitors, which are drugs used to treat cancer by blocking the inhibitory signals that prevent T cells from attacking tumor cells. By blocking CD28, these drugs can enhance the anti-tumor response of T cells and improve cancer outcomes.

CD95 (also known as Fas or APO-1) is a type of cell surface receptor that can bind to specific proteins and trigger programmed cell death, also known as apoptosis. It is an important regulator of the immune system and helps to control the activation and deletion of immune cells. CD95 ligand (CD95L), the protein that binds to CD95, is expressed on activated T-cells and can induce apoptosis in other cells that express CD95, including other T-cells and tumor cells.

An antigen is any substance that can stimulate an immune response, leading to the production of antibodies or activation of immune cells. In the context of CD95, antigens may refer to substances that can induce the expression of CD95 on the surface of cells, making them susceptible to CD95L-mediated apoptosis. These antigens could include viral proteins, tumor antigens, or other substances that trigger an immune response.

Therefore, the medical definition of 'antigens, CD95' may refer to substances that can induce the expression of CD95 on the surface of cells and make them targets for CD95L-mediated apoptosis.

CA-125 antigen is a type of protein that is found on the surface of many ovarian cancer cells and is often used as a tumor marker to monitor the effectiveness of treatment and to detect recurrence of ovarian cancer. Elevated levels of CA-125 may also be present in other types of cancer, as well as nonmalignant conditions such as endometriosis, pelvic inflammatory disease, and cirrhosis. It is important to note that while CA-125 can be a useful tool in managing ovarian cancer, it is not specific to this type of cancer and should be used in conjunction with other diagnostic tests and clinical evaluations.

Autoantibodies are defined as antibodies that are produced by the immune system and target the body's own cells, tissues, or organs. These antibodies mistakenly identify certain proteins or molecules in the body as foreign invaders and attack them, leading to an autoimmune response. Autoantibodies can be found in various autoimmune diseases such as rheumatoid arthritis, lupus, and thyroiditis. The presence of autoantibodies can also be used as a diagnostic marker for certain conditions.

Nuclear antigens are proteins or other molecules found in the nucleus of a cell that can stimulate an immune response and produce antibodies when they are recognized as foreign by the body's immune system. These antigens are normally located inside the cell and are not typically exposed to the immune system, but under certain circumstances, such as during cell death or damage, they may be released and become targets of the immune system.

Nuclear antigens can play a role in the development of some autoimmune diseases, such as systemic lupus erythematosus (SLE), where the body's immune system mistakenly attacks its own cells and tissues. In SLE, nuclear antigens such as double-stranded DNA and nucleoproteins are common targets of the abnormal immune response.

Testing for nuclear antigens is often used in the diagnosis and monitoring of autoimmune diseases. For example, a positive test for anti-double-stranded DNA antibodies is a specific indicator of SLE and can help confirm the diagnosis. However, it's important to note that not all people with SLE will have positive nuclear antigen tests, and other factors must also be considered in making a diagnosis.

Skin tests are medical diagnostic procedures that involve the application of a small amount of a substance to the skin, usually through a scratch, prick, or injection, to determine if the body has an allergic reaction to it. The most common type of skin test is the patch test, which involves applying a patch containing a small amount of the suspected allergen to the skin and observing the area for signs of a reaction, such as redness, swelling, or itching, over a period of several days. Another type of skin test is the intradermal test, in which a small amount of the substance is injected just beneath the surface of the skin. Skin tests are used to help diagnose allergies, including those to pollen, mold, pets, and foods, as well as to identify sensitivities to medications, chemicals, and other substances.

Malaria is not a medical definition itself, but it is a disease caused by parasites that are transmitted to people through the bites of infected female Anopheles mosquitoes. Here's a simple definition:

Malaria: A mosquito-borne infectious disease caused by Plasmodium parasites, characterized by cycles of fever, chills, and anemia. It can be fatal if not promptly diagnosed and treated. The five Plasmodium species known to cause malaria in humans are P. falciparum, P. vivax, P. ovale, P. malariae, and P. knowlesi.

Minor histocompatibility antigens (miHA) are proteins that exist in cells which can stimulate an immune response, particularly in the context of transplantation. Unlike major histocompatibility complex (MHC) antigens, which are highly polymorphic and well-known to trigger strong immune responses, miHA are generally less variable and may not be as immediately apparent to the immune system.

Minor histocompatibility antigens can arise from differences in genetic sequences that code for proteins outside of the MHC region. These differences can result in the production of altered or unique peptides that can be presented on the surface of cells via MHC molecules, where they may be recognized as foreign by the immune system.

In the context of transplantation, the recipient's immune system may recognize and attack donor tissues expressing these miHA, leading to graft rejection or graft-versus-host disease (GVHD). This is particularly relevant in hematopoietic stem cell transplantation (HSCT), where the transferred stem cells can differentiate into various cell types, including immune cells that may recognize and attack the recipient's tissues.

Understanding miHA and their role in transplant rejection has led to the development of strategies to minimize graft rejection and GVHD, such as T-cell depletion or targeted therapies against specific miHA.

Mansonella is a genus of filarial nematodes (roundworms) that are transmitted to humans through the bites of infected blackflies or mosquitoes. There are several species within this genus, including M. perstans, M. ozzardi, and M. streptocerca, which can cause different clinical manifestations in humans.

Mansonella perstans is the most widespread species, found mainly in Africa and some parts of Central and South America. The adult worms reside in the abdominal cavity and the thoracic cavity, where they release microfilariae into the bloodstream. This species does not usually cause severe symptoms, but chronic infection can lead to general malaise, fatigue, and peripheral eosinophilia (high levels of eosinophils in the blood).

Mansonella ozzardi is found primarily in Central and South America, and its vectors are mosquitoes. The adult worms reside in the body cavities, subcutaneous tissues, and the peritoneal cavity. Infection with M. ozzardi can cause dermatological manifestations such as pruritus (itching), papular rash, and calcified nodules under the skin.

Mansonella streptocerca is transmitted through bites of infected midges in West and Central Africa. The adult worms live in the subcutaneous tissues, particularly around the head and neck regions, leading to pruritus, papular rash, and lymphadenopathy (swollen lymph nodes).

Diagnosis of Mansonella infections is typically made through the detection of microfilariae in blood samples, often obtained during nighttime due to the nocturnal periodicity of some species. Treatment usually involves the administration of antiparasitic drugs such as ivermectin or diethylcarbamazine.

Immunohistochemistry (IHC) is a technique used in pathology and laboratory medicine to identify specific proteins or antigens in tissue sections. It combines the principles of immunology and histology to detect the presence and location of these target molecules within cells and tissues. This technique utilizes antibodies that are specific to the protein or antigen of interest, which are then tagged with a detection system such as a chromogen or fluorophore. The stained tissue sections can be examined under a microscope, allowing for the visualization and analysis of the distribution and expression patterns of the target molecule in the context of the tissue architecture. Immunohistochemistry is widely used in diagnostic pathology to help identify various diseases, including cancer, infectious diseases, and immune-mediated disorders.

Interleukin-5 (IL-5) is a type of cytokine, which is a small signaling protein that mediates and regulates immunity, inflammation, and hematopoiesis. IL-5 is primarily produced by activated T cells, especially Th2 cells, as well as mast cells, eosinophils, and innate lymphoid cells (ILCs).

The primary function of IL-5 is to regulate the growth, differentiation, activation, and survival of eosinophils, a type of white blood cell that plays a crucial role in the immune response against parasitic infections. IL-5 also enhances the ability of eosinophils to migrate from the bone marrow into the bloodstream and then into tissues, where they can participate in immune responses.

In addition to its effects on eosinophils, IL-5 has been shown to have a role in the regulation of B cell function, including promoting the survival and differentiation of B cells into antibody-secreting plasma cells. Dysregulation of IL-5 production and activity has been implicated in several diseases, including asthma, allergies, and certain parasitic infections.

A hybridoma is a type of hybrid cell that is created in a laboratory by fusing a cancer cell (usually a B cell) with a normal immune cell. The resulting hybrid cell combines the ability of the cancer cell to grow and divide indefinitely with the ability of the immune cell to produce antibodies, which are proteins that help the body fight infection.

Hybridomas are commonly used to produce monoclonal antibodies, which are identical copies of a single antibody produced by a single clone of cells. These antibodies can be used for a variety of purposes, including diagnostic tests and treatments for diseases such as cancer and autoimmune disorders.

To create hybridomas, B cells are first isolated from the spleen or blood of an animal that has been immunized with a specific antigen (a substance that triggers an immune response). The B cells are then fused with cancer cells using a chemical agent such as polyethylene glycol. The resulting hybrid cells are called hybridomas and are grown in culture medium, where they can be selected for their ability to produce antibodies specific to the antigen of interest. These antibody-producing hybridomas can then be cloned to produce large quantities of monoclonal antibodies.

HLA-B27 antigen is a type of human leukocyte antigen (HLA) found on the surface of white blood cells. HLAs are proteins that help the body's immune system distinguish its own cells from foreign substances such as viruses and bacteria.

HLA-B27 is a specific type of HLA-B antigen, which is part of the major histocompatibility complex (MHC) class I molecules. The presence of HLA-B27 antigen can be inherited from parents to their offspring.

While most people with the HLA-B27 antigen do not develop any health problems, this antigen is associated with an increased risk of developing certain inflammatory diseases, particularly spondyloarthritis, a group of disorders that affect the joints and spine. Examples of these conditions include ankylosing spondylitis, reactive arthritis, psoriatic arthritis, and enteropathic arthritis associated with inflammatory bowel disease. However, not everyone with HLA-B27 will develop these diseases, and many people without the antigen can still develop spondyloarthritis.

The Major Histocompatibility Complex (MHC) is a group of cell surface proteins in vertebrates that play a central role in the adaptive immune system. They are responsible for presenting peptide antigens to T-cells, which helps the immune system distinguish between self and non-self. The MHC is divided into two classes:

1. MHC Class I: These proteins present endogenous (intracellular) peptides to CD8+ T-cells (cytotoxic T-cells). The MHC class I molecule consists of a heavy chain and a light chain, together with an antigenic peptide.

2. MHC Class II: These proteins present exogenous (extracellular) peptides to CD4+ T-cells (helper T-cells). The MHC class II molecule is composed of two heavy chains and two light chains, together with an antigenic peptide.

MHC genes are highly polymorphic, meaning there are many different alleles within a population. This diversity allows for better recognition and presentation of various pathogens, leading to a more robust immune response. The term "histocompatibility" refers to the compatibility between donor and recipient MHC molecules in tissue transplantation. Incompatible MHC molecules can lead to rejection of the transplanted tissue due to an activated immune response against the foreign MHC antigens.

An immunoassay is a biochemical test that measures the presence or concentration of a specific protein, antibody, or antigen in a sample using the principles of antibody-antigen reactions. It is commonly used in clinical laboratories to diagnose and monitor various medical conditions such as infections, hormonal disorders, allergies, and cancer.

Immunoassays typically involve the use of labeled reagents, such as enzymes, radioisotopes, or fluorescent dyes, that bind specifically to the target molecule. The amount of label detected is proportional to the concentration of the target molecule in the sample, allowing for quantitative analysis.

There are several types of immunoassays, including enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), fluorescence immunoassay (FIA), and chemiluminescent immunoassay (CLIA). Each type has its own advantages and limitations, depending on the sensitivity, specificity, and throughput required for a particular application.

Interleukin-13 (IL-13) is a cytokine that plays a crucial role in the immune response, particularly in the development of allergic inflammation and hypersensitivity reactions. It is primarily produced by activated Th2 cells, mast cells, basophils, and eosinophils. IL-13 mediates its effects through binding to the IL-13 receptor complex, which consists of the IL-13Rα1 and IL-4Rα chains.

IL-13 has several functions in the body, including:

* Regulation of IgE production by B cells
* Induction of eosinophil differentiation and activation
* Inhibition of proinflammatory cytokine production by macrophages
* Promotion of mucus production and airway hyperresponsiveness in the lungs, contributing to the pathogenesis of asthma.

Dysregulation of IL-13 has been implicated in various diseases, such as allergic asthma, atopic dermatitis, and chronic rhinosinusitis. Therefore, targeting IL-13 with biologic therapies has emerged as a promising approach for the treatment of these conditions.

A clone is a group of cells that are genetically identical to each other because they are derived from a common ancestor cell through processes such as mitosis or asexual reproduction. Therefore, the term "clone cells" refers to a population of cells that are genetic copies of a single parent cell.

In the context of laboratory research, cells can be cloned by isolating a single cell and allowing it to divide in culture, creating a population of genetically identical cells. This is useful for studying the behavior and characteristics of individual cell types, as well as for generating large quantities of cells for use in experiments.

It's important to note that while clone cells are genetically identical, they may still exhibit differences in their phenotype (physical traits) due to epigenetic factors or environmental influences.

Hepatitis Delta Antigens (HDAg) are proteins found on the surface of the Hepatitis Delta Virus (HDV), a defective virus that requires the assistance of the Hepatitis B Virus (HBV) to replicate. There are two types of HDAg: small (S-HDAg) and large (L-HDAg). S-HDAg is a 195-amino acid protein that is essential for viral replication, while L-HDAg is a 214-amino acid protein that regulates the packaging of the viral genome into new virus particles. The presence of HDAg can be used to diagnose HDV infection and distinguish it from other forms of hepatitis.

Eosinophils are a type of white blood cell that play an important role in the body's immune response. They are produced in the bone marrow and released into the bloodstream, where they can travel to different tissues and organs throughout the body. Eosinophils are characterized by their granules, which contain various proteins and enzymes that are toxic to parasites and can contribute to inflammation.

Eosinophils are typically associated with allergic reactions, asthma, and other inflammatory conditions. They can also be involved in the body's response to certain infections, particularly those caused by parasites such as worms. In some cases, elevated levels of eosinophils in the blood or tissues (a condition called eosinophilia) can indicate an underlying medical condition, such as a parasitic infection, autoimmune disorder, or cancer.

Eosinophils are named for their staining properties - they readily take up eosin dye, which is why they appear pink or red under the microscope. They make up only about 1-6% of circulating white blood cells in healthy individuals, but their numbers can increase significantly in response to certain triggers.

Intestinal diseases refer to a wide range of conditions that affect the function or structure of the small intestine, large intestine (colon), or both. These diseases can cause various symptoms such as abdominal pain, diarrhea, constipation, bloating, nausea, vomiting, and weight loss. They can be caused by infections, inflammation, genetic disorders, or other factors. Some examples of intestinal diseases include inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), celiac disease, Crohn's disease, ulcerative colitis, and intestinal infections. The specific medical definition may vary depending on the context and the specific condition being referred to.

HLA-C antigens are a type of human leukocyte antigen (HLA) found on the surface of cells in the human body. They are part of the major histocompatibility complex (MHC) class I molecules, which play a critical role in the immune system's ability to differentiate between "self" and "non-self" cells.

HLA-C antigens are responsible for presenting peptide fragments from inside the cell to CD8+ T cells, also known as cytotoxic T lymphocytes (CTLs). This presentation allows the CTLs to recognize and destroy infected or damaged cells, helping to prevent the spread of viruses and other pathogens.

Like other HLA antigens, HLA-C antigens are highly polymorphic, meaning that there are many different variations of these molecules in the human population. This diversity allows for a better match between an individual's immune system and the pathogens they encounter, increasing the chances of mounting an effective immune response. However, this same diversity can also make it more challenging to find compatible organ donors for transplantation.

Trichostrongyloidea is a superfamily of nematode (roundworm) parasites that includes several medically and veterinarily important genera. These parasites primarily infect the gastrointestinal tract of their hosts, which can include humans, ruminants, equids, and other animals.

The life cycle of Trichostrongyloidea species typically involves eggs being passed in the feces of an infected host, hatching into larvae in the environment, and then infecting a new host through ingestion or skin penetration. The parasites then mature into adults in the host's gastrointestinal tract, where they feed on blood or tissue and cause various symptoms depending on the species and the severity of the infection.

Some common genera of Trichostrongyloidea include:
- Trichostrongylus (barber pole worm)
- Necator (human hookworms)
- Ancylostoma (hookworms that infect both humans and animals)
- Haemonchus (barber pole worm)
- Ostertagia (brown stomach worm)

Symptoms of Trichostrongyloidea infections can include abdominal pain, diarrhea, anemia, weight loss, and protein deficiency. Treatment typically involves administration of anthelmintic drugs to kill the parasites. Prevention measures include good sanitation and hygiene practices, as well as regular deworming of animals in veterinary settings.

'Onchocerca volvulus' is a species of parasitic roundworm that is the causative agent of human river blindness, also known as onchocerciasis. This disease is named after the fact that the larval forms of the worm are often found in the rivers and streams where the blackfly vectors breed.

The adult female worms measure about 33-50 cm in length and live in nodules beneath the skin, while the much smaller males (about 4 cm long) move between the nodules. The females release microfilariae, which are taken up by blackflies when they bite an infected person. These larvae then develop into infective stages within the blackfly and can be transmitted to another human host during a subsequent blood meal.

The infection leads to various symptoms, including itchy skin, rashes, bumps under the skin (nodules), and in severe cases, visual impairment or blindness due to damage caused to the eyes by the migrating larvae. The disease is prevalent in certain regions of Africa, Latin America, and Yemen. Preventive measures include avoiding blackfly bites, mass drug administration with anti-parasitic drugs, and vector control strategies.

'Brugia malayi' is a species of parasitic nematode (roundworm) that can infect humans and cause the tropical disease known as lymphatic filariasis. The adult worms typically reside in the lymphatic vessels, where they can cause inflammation, obstruction, and damage to the lymphatic system.

The life cycle of 'Brugia malayi' involves several stages, including microfilariae (immature worms) that are transmitted to a human host through the bite of an infected mosquito vector. Once inside the human body, the microfilariae migrate to the lymphatic vessels and mature into adult worms over a period of several months.

The symptoms of lymphatic filariasis can range from mild to severe, depending on the extent of the infection and the individual's immune response. In some cases, the disease can lead to chronic swelling and deformity of the affected limbs or genitalia, a condition known as elephantiasis.

Preventive measures for lymphatic filariasis include avoiding mosquito bites through the use of insect repellent, long-sleeved clothing, and bed nets, as well as mass drug administration programs to eliminate the parasite from affected communities.

Platyhelminths, also known as flatworms, are a phylum of invertebrate animals that includes free-living and parasitic forms. They are characterized by their soft, flat bodies, which lack a body cavity or circulatory system. The phylum Platyhelminthes is divided into several classes, including Turbellaria (free-living flatworms), Monogenea (ectoparasites on fish gills and skin), Trematoda (flukes, parasites in mollusks and vertebrates), and Cestoda (tapeworms, intestinal parasites of vertebrates). Platyhelminths are bilaterally symmetrical, triploblastic, and unsegmented. They have a simple digestive system that consists of a mouth and a gut, but no anus. The nervous system is characterized by a brain and a ladder-like series of nerve cords running along the length of the body. Reproduction in platyhelminths can be either sexual or asexual, depending on the species.

Humoral immunity is a type of immune response in which the body produces proteins called antibodies that circulate in bodily fluids such as blood and help to protect against infection. This form of immunity involves the interaction between antigens (foreign substances that trigger an immune response) and soluble factors, including antibodies, complement proteins, and cytokines.

When a pathogen enters the body, it is recognized as foreign by the immune system, which triggers the production of specific antibodies to bind to and neutralize or destroy the pathogen. These antibodies are produced by B cells, a type of white blood cell that is part of the adaptive immune system.

Humoral immunity provides protection against extracellular pathogens, such as bacteria and viruses, that exist outside of host cells. It is an important component of the body's defense mechanisms and plays a critical role in preventing and fighting off infections.

CD58 (also known as LFA-3) is a cell surface glycoprotein that functions as a co-stimulatory molecule in the immune system. It is found on various cells, including antigen presenting cells such as dendritic cells and B cells. CD58 interacts with its receptor, CD2, which is found on T cells, natural killer (NK) cells, and some other leukocytes. This interaction provides a costimulatory signal that helps to activate T cells and NK cells, enhancing their immune responses against pathogens or infected cells.

In the context of antigens, CD58 may be involved in presenting antigenic peptides to T cells during an adaptive immune response. The interaction between CD58 on antigen-presenting cells and CD2 on T cells contributes to the activation and proliferation of T cells specific to that particular antigen. This process is crucial for the development of effective immunity against infections and cancer.

It's important to note that while CD58 plays a role in immune responses, it is not an antigen itself. An antigen is typically defined as a molecule (usually a protein or polysaccharide) that is recognized by the adaptive immune system and can stimulate an immune response.

Oxyuroidea is a superfamily of small parasitic worms, also known as nematodes, that includes pinworms and other related species. These parasites are primarily found in the intestinal tracts of various animals, including humans, and can cause a number of health problems, such as itching, irritation, and infection.

Pinworms, which are the most common type of Oxyuroidea, are tiny white worms that live in the human colon and rectum. They are particularly common in children and can be spread easily through close contact or contaminated surfaces. Symptoms of pinworm infection may include itching around the anus, restless sleep, and irritability.

Other species of Oxyuroidea can infect a wide range of animals, including dogs, cats, and livestock. These parasites can cause similar symptoms in their hosts, such as diarrhea, weight loss, and decreased appetite. In severe cases, they can lead to more serious health problems if left untreated.

Treatment for Oxyuroidea infections typically involves the use of anti-parasitic drugs, which can help to kill the worms and alleviate symptoms. Good hygiene practices, such as washing hands frequently and cleaning contaminated surfaces, can also help to prevent the spread of these parasites.

Western blotting is a laboratory technique used in molecular biology to detect and quantify specific proteins in a mixture of many different proteins. This technique is commonly used to confirm the expression of a protein of interest, determine its size, and investigate its post-translational modifications. The name "Western" blotting distinguishes this technique from Southern blotting (for DNA) and Northern blotting (for RNA).

The Western blotting procedure involves several steps:

1. Protein extraction: The sample containing the proteins of interest is first extracted, often by breaking open cells or tissues and using a buffer to extract the proteins.
2. Separation of proteins by electrophoresis: The extracted proteins are then separated based on their size by loading them onto a polyacrylamide gel and running an electric current through the gel (a process called sodium dodecyl sulfate-polyacrylamide gel electrophoresis or SDS-PAGE). This separates the proteins according to their molecular weight, with smaller proteins migrating faster than larger ones.
3. Transfer of proteins to a membrane: After separation, the proteins are transferred from the gel onto a nitrocellulose or polyvinylidene fluoride (PVDF) membrane using an electric current in a process called blotting. This creates a replica of the protein pattern on the gel but now immobilized on the membrane for further analysis.
4. Blocking: The membrane is then blocked with a blocking agent, such as non-fat dry milk or bovine serum albumin (BSA), to prevent non-specific binding of antibodies in subsequent steps.
5. Primary antibody incubation: A primary antibody that specifically recognizes the protein of interest is added and allowed to bind to its target protein on the membrane. This step may be performed at room temperature or 4°C overnight, depending on the antibody's properties.
6. Washing: The membrane is washed with a buffer to remove unbound primary antibodies.
7. Secondary antibody incubation: A secondary antibody that recognizes the primary antibody (often coupled to an enzyme or fluorophore) is added and allowed to bind to the primary antibody. This step may involve using a horseradish peroxidase (HRP)-conjugated or alkaline phosphatase (AP)-conjugated secondary antibody, depending on the detection method used later.
8. Washing: The membrane is washed again to remove unbound secondary antibodies.
9. Detection: A detection reagent is added to visualize the protein of interest by detecting the signal generated from the enzyme-conjugated or fluorophore-conjugated secondary antibody. This can be done using chemiluminescent, colorimetric, or fluorescent methods.
10. Analysis: The resulting image is analyzed to determine the presence and quantity of the protein of interest in the sample.

Western blotting is a powerful technique for identifying and quantifying specific proteins within complex mixtures. It can be used to study protein expression, post-translational modifications, protein-protein interactions, and more. However, it requires careful optimization and validation to ensure accurate and reproducible results.

'Hymenolepis diminuta' is a species of tapeworm that infects rodents and, less commonly, humans. The adult worm typically measures 20-60 cm in length and inhabits the small intestine of its host. Infection in humans usually occurs through ingestion of infected transport hosts such as beetles or fleas, which can occur through the consumption of contaminated food or drink.

The medical definition of 'Hymenolepis diminuta' is a parasitic infection caused by the tapeworm Hymenolepis diminuta, also known as dwarf tapeworm. Symptoms of infection may include abdominal discomfort, diarrhea, and weight loss, although many infections are asymptomatic. Diagnosis is typically made through the identification of eggs or proglottids (segments of the worm) in the stool. Treatment usually involves administration of a medication called niclosamide, which kills the tapeworm. Preventive measures include practicing good hygiene and food safety habits to reduce the risk of ingesting infected transport hosts.

Ascaridida is an order of large, parasitic roundworms that belong to the phylum Nematoda. These worms are known to infect a wide range of hosts, including humans, and can cause significant damage to their host's health. The most well-known species in this order is Ascaris lumbricoides, which is the causative agent of ascariasis in humans.

Ascariasis is a common parasitic infection that affects millions of people worldwide, particularly in areas with poor sanitation and hygiene. The life cycle of Ascaris lumbricoides involves the ingestion of eggs present in contaminated food or water. Once inside the human body, the larvae hatch from the eggs and migrate through the lungs, where they mature into adult worms that can grow up to 15 inches long. The adult worms then lay thousands of eggs that are passed through the feces, perpetuating the life cycle.

Symptoms of ascariasis can range from mild to severe and may include abdominal pain, nausea, vomiting, diarrhea, and coughing. In severe cases, the worms can cause intestinal obstruction or perforation, which can be life-threatening if left untreated.

Prevention of ascariasis involves practicing good hygiene and sanitation, including washing hands thoroughly with soap and water before eating or preparing food, avoiding contact with contaminated soil or water, and cooking food thoroughly. Treatment typically involves the use of anti-parasitic drugs that kill the worms and their eggs.

CD1d is a type of antigen presenting molecule that is expressed on the surface of certain immune cells, including dendritic cells and B cells. Unlike classical MHC molecules, which present peptide antigens to T cells, CD1d presents lipid antigens to a specific subset of T cells called natural killer T (NKT) cells.

CD1d is composed of an alpha-helical heavy chain and a beta-2 microglobulin light chain, and it has a hydrophobic binding groove that can accommodate lipid antigens. CD1d-restricted NKT cells recognize and respond to these lipid antigens through their invariant T cell receptor (TCR), leading to the rapid production of cytokines and the activation of various immune responses.

CD1d-restricted NKT cells have been implicated in a variety of immunological functions, including the regulation of autoimmunity, antitumor immunity, and infectious disease.

HLA-A1 antigen is a type of human leukocyte antigen (HLA) class I molecule that plays an important role in the immune system. The HLAs are proteins found on the surface of cells that help the immune system distinguish between the body's own cells and foreign substances, such as viruses and bacteria.

The HLA-A1 antigen is one of several different types of HLA-A molecules, and it is determined by a specific set of genes located on chromosome 6. The HLA-A1 antigen is expressed on the surface of some cells in the human body and can be detected through laboratory testing.

The HLA-A1 antigen is associated with certain diseases or conditions, such as an increased risk of developing certain types of cancer or autoimmune disorders. It is also used as a marker for tissue typing in organ transplantation to help match donors and recipients and reduce the risk of rejection.

It's important to note that the presence or absence of HLA-A1 antigen alone does not determine whether someone will develop a particular disease or experience a successful organ transplant. Other genetic and environmental factors also play a role in these outcomes.

Peptides are short chains of amino acid residues linked by covalent bonds, known as peptide bonds. They are formed when two or more amino acids are joined together through a condensation reaction, which results in the elimination of a water molecule and the formation of an amide bond between the carboxyl group of one amino acid and the amino group of another.

Peptides can vary in length from two to about fifty amino acids, and they are often classified based on their size. For example, dipeptides contain two amino acids, tripeptides contain three, and so on. Oligopeptides typically contain up to ten amino acids, while polypeptides can contain dozens or even hundreds of amino acids.

Peptides play many important roles in the body, including serving as hormones, neurotransmitters, enzymes, and antibiotics. They are also used in medical research and therapeutic applications, such as drug delivery and tissue engineering.

Echinostoma is a genus of parasitic flatworms, specifically trematodes, that are known to infect various species of birds and mammals, including humans. These parasites have a complex life cycle involving multiple hosts, typically snails as the intermediate host and aquatic animals (such as fish or amphibians) as the secondary host. Humans can become infected by consuming raw or undercooked infected secondary hosts.

Echinostoma species are characterized by having a distinctive oral sucker surrounded by a collar of spines, which gives them their name (echinos means "spiny" in Greek). The adult worms live in the intestines of their definitive host and can cause symptoms such as abdominal pain, diarrhea, nausea, and vomiting. In severe cases, infection with Echinostoma species can lead to weight loss, malnutrition, and other complications.

It's worth noting that while human infections with Echinostoma species are relatively rare in developed countries, they can be more common in areas where raw or undercooked aquatic animals are consumed as part of traditional diets. Proper cooking and hygiene practices can help prevent infection with these parasites.

HLA-B7 antigen is a type of human leukocyte antigen (HLA) found on the surface of cells in our body. The HLAs are proteins that help our immune system recognize and fight off foreign substances, such as viruses and bacteria. Specifically, HLA-B7 is a class I HLA antigen, which presents peptides from inside the cell to CD8+ T cells, a type of white blood cell that plays a crucial role in the immune response.

HLA-B7 has been identified as one of the many different HLA types that can be inherited from our parents. It is located on chromosome 6 and has several subtypes. The HLA-B7 antigen is associated with certain diseases, such as ankylosing spondylitis, a type of arthritis that affects the spine. However, having this HLA type does not necessarily mean that a person will develop the disease, as other genetic and environmental factors are also involved.

It's important to note that HLA typing is used in organ transplantation to match donors and recipients and reduce the risk of rejection. Knowing a patient's HLA type can help identify compatible donors and improve the chances of a successful transplant.

Bacterial polysaccharides are complex carbohydrates that consist of long chains of sugar molecules (monosaccharides) linked together by glycosidic bonds. They are produced and used by bacteria for various purposes such as:

1. Structural components: Bacterial polysaccharides, such as peptidoglycan and lipopolysaccharide (LPS), play a crucial role in maintaining the structural integrity of bacterial cells. Peptidoglycan is a major component of the bacterial cell wall, while LPS forms the outer layer of the outer membrane in gram-negative bacteria.
2. Nutrient storage: Some bacteria synthesize and store polysaccharides as an energy reserve, similar to how plants store starch. These polysaccharides can be broken down and utilized by the bacterium when needed.
3. Virulence factors: Bacterial polysaccharides can also function as virulence factors, contributing to the pathogenesis of bacterial infections. For example, certain bacteria produce capsular polysaccharides (CPS) that surround and protect the bacterial cells from host immune defenses, allowing them to evade phagocytosis and persist within the host.
4. Adhesins: Some polysaccharides act as adhesins, facilitating the attachment of bacteria to surfaces or host cells. This is important for biofilm formation, which helps bacteria resist environmental stresses and antibiotic treatments.
5. Antigenic properties: Bacterial polysaccharides can be highly antigenic, eliciting an immune response in the host. The antigenicity of these molecules can vary between different bacterial species or even strains within a species, making them useful as targets for vaccines and diagnostic tests.

In summary, bacterial polysaccharides are complex carbohydrates that serve various functions in bacteria, including structural support, nutrient storage, virulence factor production, adhesion, and antigenicity.

HLA-DR4 is a type of human leukocyte antigen (HLA) class II histocompatibility antigen, which is found on the surface of white blood cells. It is encoded by the HLA-DRA and HLA-DRB1 genes, located on chromosome 6. The HLA-DR4 antigen includes several subtypes, such as DRB1*04:01, DRB1*04:02, DRB1*04:03, DRB1*04:04, DRB1*04:05, DRB1*04:06, DRB1*04:07, DRB1*04:08, DRB1*04:09, DRB1*04:10, DRB1*04:11, and DRB1*04:12.

The HLA-DR4 antigen plays a crucial role in the immune system by presenting peptides to CD4+ T cells, which then stimulate an immune response. This antigen is associated with several autoimmune diseases, including rheumatoid arthritis, type 1 diabetes, and multiple sclerosis. However, it's important to note that having the HLA-DR4 antigen does not necessarily mean that a person will develop one of these conditions, as other genetic and environmental factors also contribute to their development.

HLA-DR3 antigen is a type of human leukocyte antigen (HLA) class II histocompatibility antigen. HLAs are proteins found on the surface of cells that help the immune system distinguish between the body's own cells and foreign substances. The HLA-DR3 antigen is encoded by the DRB1*03:01 gene and is commonly found in individuals with certain autoimmune diseases, such as rheumatoid arthritis, type 1 diabetes, and celiac disease.

The HLA-DR3 antigen plays a role in presenting pieces of proteins (peptides) to CD4+ T cells, which are a type of white blood cell that helps coordinate the immune response. The presentation of specific peptides by the HLA-DR3 antigen can lead to an abnormal immune response in some individuals, resulting in the development of autoimmune diseases.

It's important to note that having the HLA-DR3 antigen does not guarantee that a person will develop an autoimmune disease, as other genetic and environmental factors also play a role.

The ABO blood-group system is a classification system used in blood transfusion medicine to determine the compatibility of donated blood with a recipient's blood. It is based on the presence or absence of two antigens, A and B, on the surface of red blood cells (RBCs), as well as the corresponding antibodies present in the plasma.

There are four main blood types in the ABO system:

1. Type A: These individuals have A antigens on their RBCs and anti-B antibodies in their plasma.
2. Type B: They have B antigens on their RBCs and anti-A antibodies in their plasma.
3. Type AB: They have both A and B antigens on their RBCs but no natural antibodies against either A or B antigens.
4. Type O: They do not have any A or B antigens on their RBCs, but they have both anti-A and anti-B antibodies in their plasma.

Transfusing blood from a donor with incompatible ABO antigens can lead to an immune response, causing the destruction of donated RBCs and potentially life-threatening complications such as acute hemolytic transfusion reaction. Therefore, it is crucial to match the ABO blood type between donors and recipients before performing a blood transfusion.

Agglutination tests are laboratory diagnostic procedures used to detect the presence of antibodies or antigens in a sample, such as blood or serum. These tests work by observing the clumping (agglutination) of particles, like red blood cells or bacteriophages, coated with specific antigens or antibodies when mixed with a patient's sample.

In an agglutination test, the sample is typically combined with a reagent containing known antigens or antibodies on the surface of particles, such as latex beads, red blood cells, or bacteriophages. If the sample contains the corresponding antibodies or antigens, they will bind to the particles, forming visible clumps or agglutinates. The presence and strength of agglutination are then assessed visually or with automated equipment to determine the presence and quantity of the target antigen or antibody in the sample.

Agglutination tests are widely used in medical diagnostics for various applications, including:

1. Bacterial and viral infections: To identify specific bacterial or viral antigens in a patient's sample, such as group A Streptococcus, Legionella pneumophila, or HIV.
2. Blood typing: To determine the ABO blood group and Rh type of a donor or recipient before a blood transfusion or organ transplantation.
3. Autoimmune diseases: To detect autoantibodies in patients with suspected autoimmune disorders, such as rheumatoid arthritis, systemic lupus erythematosus, or Hashimoto's thyroiditis.
4. Allergies: To identify specific IgE antibodies in a patient's sample to determine allergic reactions to various substances, such as pollen, food, or venom.
5. Drug monitoring: To detect and quantify the presence of drug-induced antibodies, such as those developed in response to penicillin or hydralazine therapy.

Agglutination tests are simple, rapid, and cost-effective diagnostic tools that provide valuable information for clinical decision-making and patient management. However, they may have limitations, including potential cross-reactivity with other antigens, false-positive results due to rheumatoid factors or heterophile antibodies, and false-negative results due to the prozone effect or insufficient sensitivity. Therefore, it is essential to interpret agglutination test results in conjunction with clinical findings and other laboratory data.

Characterization of Schistosoma japonicum egg antigens / by Wilfred Uy Tiu. by Tiu, Wilfred Uy , UNDP/World Bank/WHO Special ... Identification and characterization of circulating parasite antigens in Dirofilaria immitis infected dogs / by John Patrick ...
Evaluation of Helminth Skin-Test Antigens in a Hospital in New York City ... Polysaccharide Content of Schistosome Skin Test Antigens and the Reactivity of Nitrogenous and Carbohydrate Components ...
May 2009). "T follicular helper cells differentiate from Th2 cells in response to helminth antigens". J Exp Med. 206 (5): 991-9 ... In germinal centers, antigen-experienced TFH cells rapidly upregulate the expression of CD40L, which binds and stimulates the B ... Therefore, in the absence of TFH cells, similar to B cell activation by T-cell independent antigens, a quick burst of low ... Follicular helper T cells (also known as follicular B helper T cells and abbreviated as TFH), are antigen-experienced CD4+ T ...
The molecular basis of antigen variation. The mode of…" Nematodes "…Intestinal helminths: Epidemiology, morbidity and mortality ...
Establishment, maintenance, and antigen specificity of T cell memory in helminth infection ...
2002) An Enteric Helminth Infection Protects against an Allergic Response to Dietary Antigen. The Journal of Immunology, 169, ... b) Circulating cathodic antigen cassette test (CCA). The CCA is a semi quantitative method of detecting an active S. mansoni ... Kato Katz thick smears and circulating cathodic antigen tests were performed for S. mansoni screening, whereas thick and thin ... Anthony, M.R., Rutitzky, L.I., Urban, J.F., Stadeckerand, M.J. and Gause, W.C. (2007) Protective Immune Mechanisms in Helminth ...
Antibody-antigen interactions[edit]. The antibodys paratope interacts with the antigens epitope. An antigen usually contains ... helminths, allergens). ... Rh factor, also known as Rh D antigen, is an antigen found on ... Functions mainly as an antigen receptor on B cells that have not been exposed to antigens.[28] It has been shown to activate ... Antibodies also form complexes by binding to antigen: this is called an antigen-antibody complex or immune complex. Small ...
ICER201201 Effect of Helminth Infection on Antigen-Specific Immune Responses in Latent Tuberculosis in South India. (India, USA ... Helminth Immunology Section. Subash Babu, M.B.B.S., Ph.D. Staff Scientist, Helminth Immunology Section. Scientific Director, ... Host response to helminth infection and pathogenesis of helminthic disease *Modulation of immune responses in co-infections and ... In 2003, he was appointed as a staff scientist in the NIAID ICER program in India to continue helminth infections research work ...
It downregulates the expression of Th1 cytokines such as IFN-γ and TNF-α, MHC Class II antigens, and costimulatory molecules on ... Helminth infections are associated with marked and/or persistent eosinophilia. An increase in eosinophil levels before ... E. A. Ottesen, R. A. Hiatt, A. W. Cheever, Z. R. Sotomayor, and F. A. Neva, "The acquisition and loss of antigen-specific ... The Th1 subset is linked with cellular responses, while Th2 subset, triggered by egg-derived antigens is primarily involved in ...
Albendazole (soil-transmitted helminths). Ivermectin* (Strongyloides). Africa, non-Loaloa areas. Recommended. Recommended. ... Ndao M, Bandyayera E, Kokosin E, et Comparison of blood smear, antigen detection, and nested-PCR methods for screening from ... Soil-transmitted helminths: Albendazole 1. Strongyloidiasis: Ivermectin 1. Schistosomiasis 2:. Praziquantel 3. ... Soil-transmitted helminths: Albendazole 1. Strongyloidiasis: Ivermectin 1. Schistosomiasis 2: Praziquantel 3. ...
One way in which biologists and medics use immunotherapy is by injecting antigen-incubated Dendritic Cells (DCs) into mice to ... The vaccine DCs that reach the lymph nodes now can present melanoma-specific antigen to immature T cells which evolve into ... an 18 amino-acid peptide derived from the Helminth Taenia crassiceps [7]). Such peptide serves as an immunoadjuvant to increase ... One way in which biologists and medics use immunotherapy is by injecting antigen-incubated Dendritic Cells (DCs) into mice to ...
... circulating anodic antigen (CAA) test for S. mansoni and S. haematobium). Work primarily contributed by the Unit Diagnostics ... WHO Collaborating Centre for Epidemiology and Control of Helminth Infections More than half of the worlds population is at ... Work primarily contributed by the Group Helminths and Health.. 3. Research and development of anthelminthic drugs. In vitro and ... 1. Mapping and modelling of human helminth infections. Translate scientific work into policy, e.g. maps for control programme ...
Helminth infections induce strong type 2 cell-mediated immune responses, characterized among other things by production of high ... We can take advantage of a variety of helminth models available, each of which have their own feature including life cycle, ... A. Aldridge and S. M. ONeill, "Fasciola hepatica tegumental antigens induce anergic-like T cells via dendritic cells in a ... Parasitic helminths infect the majority of vertebrates [1]. Although parasitic helminths are near to absent in northwestern ...
Chronic helminth infection and helminth-derived egg antigens promote adipose tissue M2 macrophages and improve insulin ... Helminth infection protects against high fat diet-induced obesity via induction of alternatively activated macrophages ... Examples include derivatives from type 2 immunity/Th2/Treg-supportive helminths, shown to ameliorate obesity in mouse models ( ...
Helminths were diagnosed through stool Kato Katz examination and serum reactivity to anti-soluble adult worm antigen ... Helminths were found in 7.1% of participants on Kato Katz test, all but one of which were Schistosoma mansoni, and 32.3% of ... Mycobacterium leprae-helminth co-infections and vitamin D deficiency as potential risk factors for leprosy: A case-control ... Our results revealed M. leprae RNA and antigens persisting in the midgut and present in the ovaries of adult female A. sculptum ...
"Unwinding the role of Helminth antigen driven reprogramming of host immunity". area:. location:. Pinn 1005. type:. Seminar ...
Table 3 Helminth infections in cases with positive ICT and negative LCA. Full size table. ... Since the use of recombinant antigens is thought to produce more specific results than the use of crude antigens [11], an ICT ... In addition to their higher specificity, recombinant antigens have other important advantages over crude antigens of ... The IFAT used in this work was an in-house method implemented at the DITM, based on antigens retrieved from S. stercoralis ...
"Unwinding the role of Helminth antigen driven reprogramming of host immunity". area:. location:. Pinn 1005. type:. Seminar ...
... mansoni soluble egg antigen (SEA) and soluble (adult) worm antigen preparation (SWAP). Sensitivity and specificity were ... As an alternative, the urine-based diagnosis of schistosomiasis mansoni via the circulating cathodic antigen immuno- ... Antigens, Helminth--isolation & purification; Glycoproteins--isolation & purification; Helminth Proteins--isolation & ... mansoni soluble egg antigen (SEA) and soluble (adult) worm antigen preparation (SWAP). Sensitivity and specificity were ...
Control and elimination of helminth zoonoses in Great Mekong Subregion. Guest edited by Somphou Sayasone, Robert Bergquist, ...
Intestinal Helminths Recovered from Humans in Xieng Khouang Province, Lao PDR with a Particular Note on Haplorchis pumilio ... Advances in the Diagnosis of Human Opisthorchiasis: Development of Opisthorchis viverrini Antigen Detection in Urine. PLoS Negl ... Immune modulation by helminth parasites of ruminants: implications for vaccine development and host immune competence. Parasite ... Its rapid epithelial cell turnover seems to facilitate the rejection of intestinal helminths. In rats, it has been shown that E ...
The aim of this study was to examine the interaction between F. hepatica tegumental coat antigen and mast cells in vivo and in ... The effects of Fasciola hepatica tegumental antigens on mast cell function. by mm-red , Jun 6, 2020 ...
Helminths causing disease *worms are extracellular parasites*can release toxic wastes and antigens that can cause allergy in ... they change the antigens and act like chameleons and your immune system has to start over every time*this is called antigenic ... toxins that have been altered so that they do not act as toxins, but still act as antigens*can be used as vaccines bc they will ... punches holes in helminth body to break it up so it can be taken up by phagocytes ...
2006). Up-regulation of HLA class-I antigen expression and antigen-specific CTL response in cervical cancer cells by the ... Helminths in the Inflammation-Induced Oncogenesis. Besides the role of viral and bacterial pathogens as well as the microbiome ... which includes a large T-antigen (LT), 57kT, small T-antigen (ST) and ALTO, and also two viral coat proteins (VP1 and VP2) ( ... 2008). T antigen mutations are a human tumor-specific signature for Merkel cell polyomavirus. Proc. Natl. Acad. Sci. U.S.A. 105 ...
Helminths Helminths are multicellular and have complex organ systems. Helminths can be further divided into ... Sensitive and specific assays are now available to detect antigens of Giardia, Cryptosporidium, and Entamoeba histolytica in ... Most helminths have complex life cycles that involve substantial time outside their human hosts. A few, including Strongyloides ... In contrast to protozoa, helminths do not multiply in humans but can elicit eosinophilic responses when they migrate through ...
keywords = "Adolescent, Adult, Aged, Aged, 80 and over, Animals, Antigens, Helminth/urine, Asymptomatic Diseases, Brain/ ... We performed a pilot study of noninvasive screening for SANCC in two endemic villages in northern Peru using a urine antigen ... We performed a pilot study of noninvasive screening for SANCC in two endemic villages in northern Peru using a urine antigen ... We performed a pilot study of noninvasive screening for SANCC in two endemic villages in northern Peru using a urine antigen ...
parasite antibody; parasite antigen; praziquantel; anthelmintic agent; helminth antibody; adolesc.... MRC, Wellcome Trust; ...
Methodological limitations as well as the low attention given to the study of helminths have impacted biological research and, ... Understanding the biology of helminths using genomic and proteomic approaches could contribute to advances in understanding ... This review summarises the historical advances in functional genomics in parasitic helminths and highlights pending limitations ... host-helminth interactions and lead to new vaccines, drugs and diagnostics. Despite the significant advances in genomics in the ...
These cells have a plasmacytoid dendritic cell phenotype, a distinct response to TLR ligation and present antigen to T cells ... Tolerogenic dendritic cells in chronic helminth infection. Add to your list(s) Download to your calendar using vCal ... I have found that chronic helminth infection is associated with the expansion of CD11c(lo) dendritic cells in the draining ... CD11c(lo) cells polarise naive T cells to distinct T cells lineages, encouraging the expansion of antigen-specific Foxp3 T ...
  • Type 2 immune responses are mounted in the context of barrier disruption and entry of infectious agents, including parasites, or tissue-damaging or innocuous protein antigens, collectively termed allergens or toxins. (nature.com)
  • In most cases, the activation of ADCC involves the binding of IgG antibodies to antigens, although infestation by invasive helminths and some other parasites, IgE antibodies may be bound to the antigen on the pathogen surface. (news-medical.net)
  • The geohelminth (also known as intestinal or soil-transmitted helminth infections) parasites, Ascaris lumbricoides, Trichuris trichiura , hookworm, and Stronglyoides stercoralis , are common infectious diseases of childhood in tropical regions and are estimated to infect over 2 billion humans worldwide [ 1 ]. (biomedcentral.com)
  • Studies on the inhibition of inflammation by infection with helminth parasites have, until recently, overlooked a key determinant of health: the gut microbiota. (biomedcentral.com)
  • PURPOSE The National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), invites applications for program project (P01) grants to conduct multidisciplinary research leading to the development and evaluation of new strategies to prevent and control diseases caused by protozoan and helminth parasites. (nih.gov)
  • Th1 cells producing Interferon gamma induce cytotoxic, inflammatory responses that are most effective against intracellular parasites, whereas Th2 cells producing IL4 and IL5 induce successful responses against helminth parasites. (rochester.edu)
  • Helminth parasites co-evolve with their human host and have developed immune regulatory mechanisms whereby they harbor regulatory molecules that induce a wide range of mechanisms, such as Treg and Breg development, to blunt the attack of the host's immune system. (tum.de)
  • Helminth parasites co-evolved with human hosts and developed immune regulatory mechanisms whereby parasites harbor regulatory molecules inducing a wide range of mechanisms, such as Treg development, to evade the attack of the host's immune system, which remains silent. (tum.de)
  • She has established the importance of dendritic cell dysfunction in mediating the profound T cell hyporesponsiveness seen in parasitic helminth infection and has helped define many of the underlying mechanisms involved in this alteration of APC dysfunction. (nih.gov)
  • Dr. Gazzinelli-Guimaraes' research program has been focused on the regulation of the immune response to helminth parasitic infections and to the pathogenesis of allergic diseases. (nih.gov)
  • The presence of a helminth or other parasitic organism is indexed with the term where the helminth or other parasite is found with the subheading /parasitol not /microbiol. (nih.gov)
  • Vaccine development against parasitic helminths. (jefferson.edu)
  • Some authors consider certain species of LEECHES that can become temporarily parasitic as helminths. (bvsalud.org)
  • The inverse correlation between the geographical distribution of inflammatory bowel disease (IBD), diabetes, and multiple sclerosis with endemic parasitic helminth-infections has led to the hypothesis that infection with helminths could confer protection against auto-inflammatory disease [ 3 ]. (biomedcentral.com)
  • Parasitic helminths typically establish chronic infection, yet are generally tolerated with limited immunopathology, presumably due to their potent immunomodulatory effects [ 10 ]. (biomedcentral.com)
  • These studies aim to identify potential targets for the development of selective immunotherapy that could prevent chronic helminth infection or that could diminish allergic inflammation. (nih.gov)
  • Helminths suppress cell-mediated immunity, so we studied the effect of helminth infection and deworming on the TST in a randomized, double-blind, placebo-controlled study in an indigenous Amazon community (N = 195). (nih.gov)
  • Stool microscopy diagnosed helminths in 98% and co-infection with multiple species in 24% of study subjects. (nih.gov)
  • Thus, TST reactions were unaffected by albendazole therapy that partially cured intestinal helminth infections, and TST interpretation was unaffected by high-burden helminth infections and co-infection with multiple helminth species. (nih.gov)
  • Before hepatitis B vaccination, refugees and V93s of all ages are tested for hepatitis B virus infection by using hepatitis B surface antigen (HBsAg), where available. (cdc.gov)
  • Infection with helminths evokes changes in the composition of their host's microbiota: one outcome of which is an altered metabolome (e.g., levels of short-chain fatty acids (SCFAs)) in the gut lumen. (biomedcentral.com)
  • Having defined a feed-forward signaling loop between il-10 and butyrate following infection with H. diminuta , this study identifies the gut microbiome as a critical component of the anti-colitic effect of this helminth therapy. (biomedcentral.com)
  • The juxtaposition of helminth and bacteria in the gut allows for the possibility that the anti-inflammatory effect that follows infection with the parasite could, at least in part, be via the microbiota. (biomedcentral.com)
  • Infection sera were immunoprecipitated with excretory/secretory (ES) antigens, somatic antigen (ABF) or a purified 14kDa molecule, one of the main conponents of both ES and ABF. (gla.ac.uk)
  • This system, therefore, provides a means of studying the genetic control of antibody production in response to infection, which may identify protective antigens or resistant host haplotypes. (gla.ac.uk)
  • A feature of filarial nematode infection is a defective, T helper 2 (Th2)-polarized antigen-specific T-cell response and in relation to this we have recently shown that ES-62 inhibits clonal expansion and modulates effector function towards a Th2 phenotype, of antigen-specific T cells in vivo. (gla.ac.uk)
  • IFN-γ, TNF-α, T H 1 cells), whereas infection by helminths typically elicits a type II host resistance and tolerizing immune response (e.g. (biomedcentral.com)
  • Indeed, recent studies indicate that infection by helminths differentially shapes the response and outcome of subsequent infection by viruses and bacteria. (biomedcentral.com)
  • Rather than an exhaustive summary of the literature, our goal in this review is to provide some key concepts and emphasize existing issues in relation to helminth as a friend or foe in bacterial or viral infection. (biomedcentral.com)
  • While T H 2 responses limit helminth infection and can result in the physical expulsion from the mucosal membranes in which they reside, helminths are rarely killed. (biomedcentral.com)
  • Chronic helminth infection induces a type-2 cellular immune response. (ox.ac.uk)
  • Moreover, this demonstration that helminth infection in humans can modulate the immune response to a concurrent infection or immunological challenge is of critical importance to future vaccination strategies. (ox.ac.uk)
  • The Geshiyaro project is a 5-year intervention to assess the impact of community- and school-based water, sanitation, and hygiene (WaSH) interventions on reducing infection with soil-transmitted helminths (STH. (biomedcentral.com)
  • How can a chronic helminth infection have an impact on a vaccine? (tum.de)
  • The evidence from our working group's animal models demonstrates that co-infection with helminths profoundly affects immune responses to bystander antigens including vaccines. (tum.de)
  • Study data highlight the important differences between the immune responses to natural helminth infection and to vaccination with a recombinant helminth antigen. (johnshopkins.edu)
  • Therefore, in the absence of TFH cells, similar to B cell activation by T-cell independent antigens, a quick burst of low affinity plasma cell production is formed but this does not lead to germinal center induction nor permit antibody affinity maturation or the differentiation of effective memory B cells which are essential in fortifying the body against subsequent infections. (wikipedia.org)
  • The regulation of host immunity by chronic geohelminth infections may not just affect responses to parasite antigens but also other exogenous antigens such as the antigenic constituents of vaccines and aeroallergens. (biomedcentral.com)
  • Helminth infections characteristically, induce high titres of IgE and special attention was, therefore, focused on the production and control of IgE, in this model, Parasite-specific IgE was examined using passive cutaneous anaphylaxis (PCA) and IgE-specific Western blotting. (gla.ac.uk)
  • These responses include the serum IgG1 and IgE responses, the secretory IgA response, and eosinophil-mediated inflammatory responses, such as occur during gut helminth infections and allergic responses, including asthma. (nih.gov)
  • In this review, we summarize the current knowledge on how helminth infections influence concurrent or subsequent microbial infections and also discuss the implications for helminth-mediated immunity on the outcome of SARS-CoV-2 disease. (biomedcentral.com)
  • The importance of the T H 2 response in helminth immunity is supported by population genetic associations between loci that control T H 2 responses or their effector cytokines and susceptibility to worm infections [ 13 ]. (biomedcentral.com)
  • Gastrointestinal (GI) infections can be caused by many types of microbes, including bacteria, viruses, protozoa, and helminths. (nih.gov)
  • The present study examines the immune responses of children exposed to both the helminth parasite Onchocerca volvulus and the mycobacterial infections, Mycobacterium tuberculosis and M. leprae. (ox.ac.uk)
  • Gastrointestinal (GI) helminth infections cause significant morbidity in both humans and animals worldwide. (biomedcentral.com)
  • Collectively, the stage for antigen avoidance is set when adaptive immunity equips mast cells with IgE as a telltale of past immune responses. (nature.com)
  • Prevention of immunopathology-causing, continuous and futile responses against per se innocuous antigens or of repeated ingestion of toxins through mast-cell-mediated antigen-avoidance behaviour may be an important arm of immunity. (nature.com)
  • Type 2 immune responses, notably involving interleukin (IL)-4, drive immunoglobulin class switch recombination to antigen-specific IgE, which is bound to the mast-cell-expressed high-affinity IgE receptor (FcεRI). (nature.com)
  • Immunoglobulin (Ig) G responses to several antigens/pathogens were assessed by a multiplex bead assay (MBA), and the recombinant Taenia solium T24H antigen was included. (nih.gov)
  • 3. IFNG-mediated immune responses enhance autophagy against Mycobacterium tuberculosis antigens in patients with active tuberculosis. (nih.gov)
  • 16. Characterization of human cellular immune responses to novel Mycobacterium tuberculosis antigens encoded by genomic regions absent in Mycobacterium bovis BCG. (nih.gov)
  • The basis of the vaccines will the combination of recombinant antigens with adjuvants capable of inducing specific types of immune responses. (jefferson.edu)
  • The epithelial cell barrier is often the first line of defense against helminths, but also provides signals that instruct dendritic cells (DCs), group 2 innate lymphoid cells (ILC2s), and T H 2 cells to produce type 2 immune responses [ 19 ]. (biomedcentral.com)
  • In response to helminths or ensuing mast cells responses, intestinal epithelial cells (IECs) release IL-33, which binds to its receptor, ST2 (suppression of tumorigenicity 2), to activate a wide range of immune cells and elicit the production of type 2 cytokines by ILC2s, T H 2 cells, basophils, and mast cells. (biomedcentral.com)
  • Some of these molecules have been identified as regulators for each phase of the host immune response: initiation, antigen recognition and processing, adaptive and effector cell responses and tissue remodeling and repair. (tum.de)
  • Dendritic cells (DCs) are antigen-presenting cells that regulate T cell responses for many infectious diseases. (biomedcentral.com)
  • Dendritic cells (DCs) are antigen presenting cells that play a pivotal role in the control and modulation of immune responses by initiating T cell responses and producing cytokines and other molecules that regulate adaptive immunity [ 21 ]. (biomedcentral.com)
  • Acquired immunity against helminths is characterised by a complex interplay between the effector Th1 and Th2 immune responses and it slowly manifests with age as a result of cumulative exposure to parasite antigens. (lshtm.ac.uk)
  • These data advance knowledge of vaccine development for helminths given their propensity to induce strong T H 2 responses. (johnshopkins.edu)
  • Ability of an organism to recognize and defend itself against specific pathogens or antigens. (powershow.com)
  • Genes encoding protective antigens from different pathogens can be cloned and expressed in salmonella vaccine strains, which are then used to piggy back these antigens to the mucosal and systemic immune systems via oral immunisation. (bmj.com)
  • Within germinal centers, TFH cells play a critical role in mediating the selection and survival of B cells that go on to differentiate either into long-lived plasma cells capable of producing high affinity antibodies against foreign antigen, or germinal center-dependent memory B cells capable of quick immune re-activation in the future if ever the same antigen is re-encountered. (wikipedia.org)
  • The switched antibodies acquire better effector functions, and hypermutated antibody shows greater affinity for antigen. (wikipedia.org)
  • Detection of Immunoglobulin G Antibodies to Taenia solium Cysticercosis Antigen Glutathione-S-Transferase-rT24H in Malian Children Using Multiplex Bead Assay. (nih.gov)
  • Allergic reactions in affected individuals following meat consumption are mediated predominantly by IgE antibodies specific for galactose-α-1,3-galactose (α-gal), a blood group antigen of non-primate mammals and therefore present in dietary meat. (frontiersin.org)
  • First, the B-cell produces antibodies directed against specific antigens present on a pathogen or a foreign body. (news-medical.net)
  • These antibodies bind to the target antigen and the constant region of the antibody (Fc) is recognized by the effector cells of the immune system via Fc receptors on their surfaces. (news-medical.net)
  • ADCC is invoked when antibodies bind with both the antigen present on the target cell and Fc receptors on the effectors cells of the host. (news-medical.net)
  • On the other hand, the ELISA technique was used to study the response of IgG antibodies against E/S antigens of D. dendriticum in the sera of 40 sheep. (tubitak.gov.tr)
  • Mucosal mast cells lining the stomach and small intestine rapidly sensed antigen ingestion. (nature.com)
  • On subsequent antigen ingestion, mast cells signal termination of antigen intake. (nature.com)
  • Mucosal mast cells lining the stomach and small intestine rapidly respond to ingested antigens. (nature.com)
  • Mice harbouring mast cells but not mast-cell-deficient mice subsequently avoid antigen uptake when given a free choice of water with or without antigen under unperturbed behavioural conditions. (nature.com)
  • Follicular helper T cells (also known as follicular B helper T cells and abbreviated as TFH), are antigen-experienced CD4+ T cells found in the periphery within B cell follicles of secondary lymphoid organs such as lymph nodes, spleen and Peyer's patches, and are identified by their constitutive expression of the B cell follicle homing receptor CXCR5. (wikipedia.org)
  • In germinal centers, antigen-experienced TFH cells rapidly upregulate the expression of CD40L, which binds and stimulates the B cell surface receptor CD40. (wikipedia.org)
  • We have a specific interest in understanding the plasticity and specificity of circulating peripheral and tissue-resident effector Th2 cells driven by helminth antigens and/or allergens, as well as to understand the role of the effector Th2 subsets in the establishment of tissue Type-2-mediated inflammation using both mouse models and human studies. (nih.gov)
  • 5. [Th2 differentiation features of Mycobacterium tuberculosis heat resistant antigen-activated human γδT cells and the regulation of transcription factor T-bet/GATA-3 on differentiation]. (nih.gov)
  • Some target cells express the Fas antigen, which is then engaged by a host cell molecule called Fas ligand. (news-medical.net)
  • A lower percentage of antigen-presenting cells (APCs) was detected with respect to the UC. (biomedcentral.com)
  • Marshall, F. A. , Watson, K. A. , Garside, P. , Harnett, M. M. and Harnett, W. (2008) Effect of activated antigen-specific B cells on ES-62-mediated modulation of effector function of heterologous antigen-specific T cells in vivo. (gla.ac.uk)
  • We have recently found that stimulation of the retinoid X receptor (RXR) pathway in antigen-naive Th0 cells promotes development of Th2 memory cells (as indicated by the production of IL-4), while stimulation of the retinoic acid receptor (RAR) pathway does not. (nih.gov)
  • These primed, precursor cells (Thpp) produce IL-2 and proliferate rapidly, allowing expansion of antigen-specific cells during an immune response before commitment to a particular effector phenotype. (rochester.edu)
  • Proliferation of peripheral blood mononuclear cells (PBMC) and production of IL-4 in response to both helminth and mycobacterial antigen (PPD) decreased dramatically with increasing microfilarial (MF) density. (ox.ac.uk)
  • B Cells Enhance Antigen-Specific CD4 T Cell Pr. (prolekarniky.cz)
  • Description: The DX5 monoclonal antibody reacts with CD49b, an antigen expressed on a majority of mouse natural killer cells and a subset of T cells. (thermofisher.com)
  • Activation of invariant NKT cells by the helminth parasite schistosoma mansoni. (ox.ac.uk)
  • Taken together, our data show for the first time that helminths can activate iNKT cells to produce immunoregulatory cytokines in vivo, enabling them to influence the adaptive immune response. (ox.ac.uk)
  • The diag nostic value o f W. bancrofti microflarial antigen in chronic cases has been discussed. (jpgmonline.com)
  • Helminth antigens were investigated in the search for accessible heterologous antigens capable to discriminate different helminthiases, by the enzyme linked immunosorbent assay (ELISA) and the immunoblot assay (IB). (nih.gov)
  • Furthermore, the use of precisely attenuated bacterial vectors as carriers for recombinant heterologous antigens can lead to the generation of multivalent vaccines. (bmj.com)
  • Wuchereria bancrofti microfilarial antigen was investigated in skin test on: (1) Microfilaria carriers, (2) Amicrofilaraemic cases from endemic villages with and without intestinal helminths, (3) Cases having apparent symptoms and signs of filariasis. (jpgmonline.com)
  • Live attenuated salmonella vaccines are useful vectors for the delivery of recombinant antigens to the immune system. (bmj.com)
  • 1 The most effective way to induce local immunity against infectious agents has so far proved to be direct application of vaccine antigens to mucosal surfaces (oral or intranasal delivery). (bmj.com)
  • However, clinical studies in humans have so far not yielded a clear picture due to many overlapping helminth, vaccine, and study design factors, and the diverse characteristics of the populations that are studied. (tum.de)
  • In contrast, helminths stimulate potent type 2 immune response, which results in clearance and/or tolerance to helminths, and includes anti-inflammatory and wound healing programs. (biomedcentral.com)
  • Onchocerciasis modulates the immune response to mycobacterial antigens. (ox.ac.uk)
  • The rapid diagnostic tests (RDTs), point of care circulating cathodic antigen (POC-CCA) and Hemastix, were used to estimate Schistosoma mansoni and Schistosoma haematobium prevalence, respectively. (infontd.org)
  • 2 The fact that we have so few effective oral vaccines shows that the induction of protective immunity through oral immunisation is not an easy goal to achieve as many antigens are poor oral immunogens. (bmj.com)
  • Oral vaccines can be based on either live or non-living antigens. (bmj.com)
  • hence, we identify the immunological sensor cell linking antigen recognition to avoidance behaviour. (nature.com)
  • This restricted recognition could however, be overcome if a purified antigen was presented with adjuvant. (gla.ac.uk)
  • The tuberculin skin test (TST) quantifies cell-mediated immunity to tuberculosis antigens. (nih.gov)
  • 8. In vitro levels of cytokines in response to purified protein derivative (PPD) antigen in a population with high prevalence of pulmonary tuberculosis. (nih.gov)
  • Avoidance prevented antigen-driven adaptive, innate and mucosal immune activation and inflammation in the stomach and small intestine. (nature.com)
  • 1. Lactic acid bacteria enhance autophagic ability of mononuclear phagocytes by increasing Th1 autophagy-promoting cytokine (IFN-gamma) and nitric oxide (NO) levels and reducing Th2 autophagy-restraining cytokines (IL-4 and IL-13) in response to Mycobacterium tuberculosis antigen. (nih.gov)
  • 12. Helminth Antigen Exposure Enhances Early Immune Control of Mycobacterium tuberculosis in Monocytes and Macrophages. (nih.gov)
  • 17. Cytokine profiles for peripheral blood lymphocytes from patients with active pulmonary tuberculosis and healthy household contacts in response to the 30-kilodalton antigen of Mycobacterium tuberculosis. (nih.gov)
  • Any part or derivative of a helminth that elicits an immune reaction. (nih.gov)
  • 1987). Assessment of a condition of amicrofilaremic or occult dirofilariasis was determined by necropsies, knott's and antibody-ELISA and antigen-ELISA. (vin.com)
  • Suspected cases were further tested by modified knott's concentration and/or antigen-ELISA kits (Snap R , Idexx, U.S.A. and Witness R , Agen, Australia). (vin.com)
  • It is proved that the antigen-ELISA detection is superior over conventional methods and gave 30.9% better result than those conventional ones. (vin.com)
  • The EG95 antigen of Echinococcus spp. (ac.ir)
  • A gene family expressing a host-protective antigen of Echinococcus granulosus. (ac.ir)
  • Helminths including nematodes, cestodes and trematodes, are handled differently by the host immune system compared to bacteria or viruses. (biomedcentral.com)
  • Invertebrates include insects and helminths. (nih.gov)
  • We suggest that any intention-to-treat with helminth therapy should be based on the characterization of the patient's immunological and microbiological response to the helminth. (biomedcentral.com)
  • Moreover, the cross-reactivity among helminthiases was found with the use of antigens belonging to phylogenetically related parasite species, Eg, Tso and Tcra-VF, by sharing same antigenic components. (nih.gov)
  • The functional implications of helminth-evoked changes in the enteric microbiome (composition and metabolites) are poorly understood and are explored with respect to controlling enteric inflammation. (biomedcentral.com)
  • Protein bands of excretory/secretory (E/S) antigens of Dicrocoelium dendriticum were determined using SDS-PAGE and Western blotting. (tubitak.gov.tr)
  • In the SDS-PAGE analysis of D. dendriticum E/S antigen, 9 protein bands with molecular weights varying between 6 and 66 kDa with Coomassie staining and 14 bands between 6 and 205 kDa with silver staining were detected. (tubitak.gov.tr)
  • Identification and characterization of membrane antigen may constitute an alternative source of antigen and then assist the development of serological techniques. (usp.br)
  • Thus, it is thought that exposure to tick bites promotes cutaneous sensitization to tick antigens such as α-gal, leading to the development of IgE-mediated meat allergy. (frontiersin.org)