Leukocytes
Neutrophils
Leukocytes, Mononuclear
Chemotaxis, Leukocyte
Phagocytosis
Leukocyte Count
N-Formylmethionine Leucyl-Phenylalanine
P-Selectin
Monocytes
Venules
Antigens, CD18
Inflammation
Blood Bactericidal Activity
Phagocyte Bactericidal Dysfunction
Cells, Cultured
Lymphocytes
Neutrophil Activation
Flow Cytometry
L-Selectin
Granulocytes
Zymosan
Leukotriene B4
Chemotactic Factors
Intercellular Adhesion Molecule-1
Macrophages
Endothelium, Vascular
Luminescent Measurements
Cell Adhesion Molecules
Opsonin Proteins
Selectins
Leukocyte Transfusion
Peroxidase
Rabbits
Oxyquinoline
Macrophage-1 Antigen
Arachidonate Lipoxygenases
Superoxides
N-Formylmethionine
Alismataceae
E-Selectin
Arachidonate 5-Lipoxygenase
Luminol
Blood Platelets
Respiratory Burst
Antigens, CD
Chemokines
Cytokines
Tumor Necrosis Factor-alpha
RNA, Messenger
Lipopolysaccharides
Molecular Sequence Data
Complement C5a
Interleukin-8
Indium
Disease Models, Animal
Mice, Knockout
T-Lymphocytes
Cell Migration Assays, Leukocyte
Platelet Activating Factor
Complement C5
Eosinophils
Nitroblue Tetrazolium
Neutrophil Infiltration
HL-60 Cells
Vascular Cell Adhesion Molecule-1
Leukotriene A4
Lymphocyte Function-Associated Antigen-1
Erythrocytes
Cell Communication
Lung
Peritonitis
Blood Proteins
Receptors, Chemokine
Peroxidases
Leukotrienes
Receptors, Formyl Peptide
Chemotaxis
Granulomatous Disease, Chronic
Arachidonic Acids
Microscopy, Video
Endothelial Cells
Pancreatic Elastase
Muramidase
Chediak-Higashi Syndrome
Tetradecanoylphorbol Acetate
Hydrogen Peroxide
Antigens, CD11
Polymerase Chain Reaction
Base Sequence
Exudates and Transudates
Chemokine CCL2
Microscopy, Electron
Hydroxyeicosatetraenoic Acids
Amino Acid Sequence
Endotoxins
Interleukin-1
Capillary Permeability
Integrin alpha4
Cell Migration Inhibition
Glucuronidase
Lactoferrin
Lipoxins
Leukopenia
Cell Membrane
Inflammation Mediators
Complement System Proteins
Antigens, CD31
Transendothelial and Transepithelial Migration
Cattle
Skin
Calcimycin
Chemokines, CXC
Guinea Pigs
Antigens, CD11b
Endothelium
Immunohistochemistry
Signal Transduction
Gene Expression Regulation
Leukocyte Adherence Inhibition Test
Reverse Transcriptase Polymerase Chain Reaction
Receptors, Leukocyte-Adhesion
Lymphocyte Activation
Cell Aggregation
Hexosephosphates
Antigens, CD45
Dose-Response Relationship, Drug
Acridine Orange
Peritoneal Cavity
Mannheimia haemolytica
Technetium Tc 99m Exametazime
Immune Sera
Chemokine CXCL1
Gene Expression
Bone Marrow Cells
Bone Marrow
Abscess
Focal Infection
Antigens, Differentiation, Myelomonocytic
Cell Count
Receptors, Complement
Antigens, CD15
Receptors, Cell Surface
Up-Regulation
Latex
Reperfusion Injury
Immunity, Innate
Escherichia coli
Colchicine
Antigens, CD53
Integrin alpha4beta1
Interferon-gamma
Basophils
Killer Cells, Natural
Leukostasis
Cytomegalovirus Infections
Staphylococcus aureus
Hydroxyquinolines
Arachidonic Acid
Antigens, CD43
Defensins
Lipoxygenase
Chemokine CCL5
Pleurisy
Integrins
Enzyme-Linked Immunosorbent Assay
Receptors, Leukotriene B4
Phagocytic acitivity of bovine leukocytes during pregnancy. (1/9769)
The phagocytic competence, measured as the total number of polymorphonuclear leukocytes per mm3 which phagocytosed Staphylococcus aureus, strain 321, in vitro, was determined in eight cows during complete pregnancies. Such leukocytes are referred to as "Active PMN'S". There was a gradual decline in the number of these cells from conception to a minimum between the 16th and 20th weeks of pregnancy, followed by a steady increase to the cessation of lactation when a marked drop occurred, after which there was an increase to a maximun during the second week prepartum. From this maximum there was a rapid decrease to an absolute minimum during the first week after parturition. From the second week postpartum there was a gradual increase to conception. The correlation coefficient (r) of number of active PMN'S with time before conception was -0.474 )p-0.01). There were significant differences (p=0.01) in numbers of active PMNS Among the eight cows. It was found that the cows fell into two groups, one whose members had, overall, significantly more active PMNs (p=0.001) than those in the second group. The between cow differences may have been due to 1) age, since the cows with the highest numbers of circulating active PMNs were younger than those in the other group of 2) the combined stress of pregnancy and lactation, as those cows which were both pregnant and milking had the lowest numbers of active PMNs. (+info)Blocking very late antigen-4 integrin decreases leukocyte entry and fatty streak formation in mice fed an atherogenic diet. (2/9769)
Atherosclerotic lesion development is characterized by the recruitment of leukocytes, principally monocytes, to the vessel wall. Considerable interest has been focused on the adhesion molecule(s) involved in leukocyte/endothelial interactions. The goal of the present study was to determine the role of the very late antigen-4 (VLA-4) integrin/ligand interaction in fatty streak development using murine models. Because alpha4 null mice are not viable, a peptidomimetic was used to block VLA-4-mediated leukocyte binding. The ability of a synthetic peptidomimetic of connecting segment-1 (CS-1 peptide) to block the recruitment of leukocytes and the accumulation of lipid in the aortic sinus of either wild-type mice (strain C57BL/6J) or mice with a low-density lipoprotein null mutation (LDLR-/-) maintained on an atherogenic diet was assessed. The active (Ac) CS-1 peptide or scrambled (Sc) CS-1 peptide was delivered subcutaneously into mice using a mini osmotic pump. Mice were exposed to the peptide for 24 to 36 hours before the onset of the atherogenic diet. In C57BL/6J mice, leukocyte entry into the aortic sinus, as assessed by en face preparations, was inhibited by the active peptide (Ac=28+/-4, Sc=54+/-6 monocytes/valve; P=0.004). Additionally, frozen sections stained with Oil Red O were analyzed to assess lipid accumulation in the aortic sinus. C57BL/6J mice that received the (Ac) compound demonstrated significantly reduced lesion areas as compared with mice that received the (Sc) peptide (Ac=4887+/-4438 microm2, Sc=15 009 +/-5619 microm2; P<0.0001). In a separate study, LDLR-/- mice were implanted with pumps containing either the (Ac) or (Sc) peptide before initiation of the atherogenic diet. Because LDLR-/- mice fed a chow diet displayed small lesions at 14 weeks, the effects of the peptide seen in these animals represented a change in early lipid accumulation rather than initiation. By using whole-mount preparations, the (Ac) but not the (Sc) peptide significantly reduced the area of lipid accumulation in the aortic sinus, resulting in an approximate 66% decrease. Plasma analysis from all studies revealed concentrations of peptide to be present at levels previously determined by in vitro analysis to block adhesion. (Ac) CS-1 peptide, which blocks VLA-4 on the leukocyte surface, is effective in reducing leukocyte recruitment and lipid accumulation in the aortic sinus. The present study provides in vivo evidence that the VLA-4 integrin plays an important role in the initiation of the atherosclerotic lesion and lipid accumulation, and it suggests a potential therapeutic strategy for this disease. (+info)Inhibition of L-selectin-mediated leukocyte rolling by synthetic glycoprotein mimics. (3/9769)
Synthetic carbohydrate and glycoprotein mimics displaying sulfated saccharide residues have been assayed for their L-selectin inhibitory properties under static and flow conditions. Polymers displaying the L-selectin recognition epitopes 3',6-disulfo Lewis x(Glc) (3-O-SO3-Galbeta1alpha4(Fucalpha1alpha3)-6-O-SO3-Glcbeta+ ++-OR) and 3',6'-disulfo Lewis x(Glc) (3, 6-di-O-SO3-Galbeta1alpha4(Fucalpha1alpha3)Glcbeta-OR) both inhibit L-selectin binding to heparin under static, cell-free binding conditions with similar efficacies. Under conditions of shear flow, however, only the polymer displaying 3',6-disulfo Lewis x(Glc) inhibits the rolling of L-selectin-transfected cells on the glycoprotein ligand GlyCAM-1. Although it has been shown to more effective than sialyl Lewis x at blocking the L-selectin-GlyCAM-1 interaction in static binding studies, the corresponding monomer had no effect in the dynamic assay. These data indicate that multivalent ligands are far more effective inhibitors of L-selectin-mediated rolling than their monovalent counterparts and that the inhibitory activities are dependent on the specific sulfation pattern of the recognition epitope. Importantly, our results indicate the L-selectin specificity for one ligand over another found in static, cell-free binding assays is not necessarily retained under the conditions of shear flow. The results suggest that monovalent or polyvalent carbohydrate or glycoprotein mimetics that inhibit selectin binding in static assays may not block the more physiologically relevant process of selectin-mediated rolling. (+info)Changes in haematological parameters and iron metabolism associated with a 1600 kilometre ultramarathon. (4/9769)
OBJECTIVE: To investigate haematological variations and iron related changes in the serum of participants in a 1600 kilometre ultramarathon run. PARTICIPANTS: Seven male and two female participants in a 1600 km foot race. METHODS: Blood samples were obtained from the participants before, after four and 11 days of running, and at the end of the event. Samples were analysed by standard methods for haemoglobin, packed cell volume, total red cell count, mean red cell volume, mean red cell haemoglobin, total white cell count and differential, platelets, reticulocytes, iron, ferritin, total iron binding capacity, percentage transferrin saturation, haptoglobin, and bilirubin and corrected for changes in plasma volume. RESULTS: The following variables decreased during the event (p < 0.05): haemoglobin, packed cell volume, mean red cell volume, percentage lymphocytes, percentage monocytes, serum iron, total iron binding capacity, and percentage transferrin saturation. Increases (p < 0.05) were found in plasma volume, total red cell count (day 4 only), total white cell count, percentage and absolute numbers of neutrophils and reticulocytes, absolute numbers of lymphocytes and monocytes (day 4 only), absolute numbers of eosinophils (day 11 and race end), absolute numbers of basophils (race end only), platelets, ferritin, haptoglobin, and bilirubin (day 4 only). CONCLUSION: Ultramarathon running is associated with a wide range of changes in haematological parameters, many of which are related to the normal acute phase response to injury. These should not be confused with indicators of disease. (+info)Phenotypic and functional studies of leukocytes in human endometrium and endometriosis. (5/9769)
The aetiology of endometriosis, a common and disabling disorder, is presently unknown, although immune dysfunction could allow ectopic endometrial fragments to survive outside the uterine cavity. These studies investigate the relationship between leukocyte populations, steroid hormone receptor expression, proliferative activity, bcl-2 expression and apoptosis in eutopic and ectopic endometrium from women with endometriosis or adenomyosis at different phases of the menstrual cycle. Significantly increased oestrogen receptor expression, bcl-2 expression and numbers of CD8+ leukocytes were found in ectopic compared with eutopic endometrium in endometriosis, and CD56+ endometrial granulated lymphocytes (eGLs) were significantly reduced in ectopic endometrium. Apoptotic cells were rarely found in control and subject endometria. In contrast with endometriosis, adenomyotic lesions showed identical steroid hormone receptor expression, proliferative activity, bcl-2 expression and leukocyte subpopulations to eutopic endometrium, indicating different aetiologies for these disorders. The unusual CD56+ CD16- eGLs present in large numbers in late secretory phase eutopic endometrium were highly purified (>98%) by immunomagnetic separation. Except for a negligible cytotoxic activity of eGLs from early proliferative samples, cytotoxic activity of eGLs from non-pregnant endometrium during the menstrual cycle was comparable with those in peripheral blood, predominantly CD56+ CD16+ natural killer cells. eGLs from non-pregnant endometrium and early pregnancy showed a variable proliferative response to 5 and 100 U/ml interleukin-2 over 48-h and 120-h time courses. eGLs are evidently functionally important in the eutopic endometrium. Their absence in endometriotic lesions together with increased CD+8 T-cell numbers and increased oestrogen receptor and bcl-2 expression may have significant effects on the development and progression of endometriosis. (+info)Differential expression and phosphorylation of CTCF, a c-myc transcriptional regulator, during differentiation of human myeloid cells. (6/9769)
CTCF is a transcriptional repressor of the c-myc gene. Although CTCF has been characterized in some detail, there is very little information about the regulation of CTCF activity. Therefore we investigated CTCF expression and phosphorylation during induced differentiation of human myeloid leukemia cells. We found that: (i) both CTCF mRNA and protein are down-regulated during terminal differentiation in most cell lines tested; (ii) CTCF down-regulation is retarded and less pronounced than that of c-myc; (iii) CTCF protein is differentially phosphorylated and the phosphorylation profiles depend on the differentiation pathway. We concluded that CTCF expression and activity is controlled at transcriptional and post-transcriptional levels. (+info)Identification of a novel activation-inducible protein of the tumor necrosis factor receptor superfamily and its ligand. (7/9769)
Among members of the tumor necrosis factor receptor (TNFR) superfamily, 4-1BB, CD27, and glucocorticoid-induced tumor necrosis factor receptor family-related gene (GITR) share a striking homology in the cytoplasmic domain. Here we report the identification of a new member, activation-inducible TNFR family member (AITR), which belongs to this subfamily, and its ligand. The receptor is expressed in lymph node and peripheral blood leukocytes, and its expression is up-regulated in human peripheral mononuclear cells mainly after stimulation with anti-CD3/CD28 monoclonal antibodies or phorbol 12-myristate 13-acetate/ionomycin. AITR associates with TRAF1 (TNF receptor-associated factor 1), TRAF2, and TRAF3, and induces nuclear factor (NF)-kappaB activation via TRAF2. The ligand for AITR (AITRL) was found to be an undescribed member of the TNF family, which is expressed in endothelial cells. Thus, AITR and AITRL seem to be important for interactions between activated T lymphocytes and endothelial cells. (+info)A sialoglycoprotein, gp20, of the human capacitated sperm surface is a homologue of the leukocyte CD52 antigen: analysis of the effect of anti-CD52 monoclonal antibody (CAMPATH-1) on capacitated spermatozoa. (8/9769)
In this study we performed N-terminal sequence analysis of gp20, a 20 kDa sialoglycoprotein on the human sperm surface previously identified by radiolabelling of the sialic acid residues of sperm surface. We found 100% identity with the N-terminus of CD52, an antigen expressed on almost all human leukocytes. We also show that, like CD52, gp20 behaves as a glycosylphosphatidylinositol (GPI)-anchored protein and that anti-gp20 antiserum reacts with an antigen on leukocytes of the same molecular weight as CD52. Using CAMPATH-1, the monoclonal antibody against CD52, in fluorescent staining of capacitated spermatozoa, Western blot analysis and the zona-free hamster egg penetration test, we found that the effect of this antibody was different from that of our anti-gp20. Western blot analysis revealed a well-defined 20 kDa band with anti-gp20, whereas a 14-20 kDa band was detected with CAMPATH-1. Anti-gp20 stained the equatorial region of the sperm head, whereas CAMPATH-1 stained the tail in immunofluorescence analysis of capacitated spermatozoa. A dose-dependent inhibitory effect was seen with CAMPATH-1, similar to that previously detected with anti-gp20, in a zona-free hamster egg penetration test. However, with CAMPATH-1 agglutination of motile spermatozoa was detected, and this was not present with anti-gp20. This suggests that the epitopes recognized by the two antibodies are different. (+info)N-Formylmethionine Leucyl-Phenylalanine (fMLP) is a synthetic peptide that mimics the activity of a naturally occurring bacterial peptide called N-formylmethionine. It is commonly used in the medical field as a chemoattractant for neutrophils, a type of white blood cell that plays a key role in the body's immune response. fMLP is typically administered intravenously or intraperitoneally, and its effects are rapid and short-lived. It is often used in research studies to investigate the mechanisms of neutrophil recruitment and activation, as well as to test the efficacy of new drugs and therapies for inflammatory and infectious diseases. In addition to its use as a chemoattractant, fMLP has also been studied for its potential therapeutic applications in a variety of conditions, including sepsis, acute respiratory distress syndrome, and cancer. However, more research is needed to fully understand its potential benefits and risks in these contexts.
P-selectin is a type of adhesion molecule that plays a crucial role in the process of inflammation and thrombosis. It is expressed on the surface of activated platelets and endothelial cells, and it binds to a specific receptor on the surface of leukocytes, allowing them to adhere to the blood vessel wall and migrate into the site of inflammation or injury. P-selectin is also involved in the recruitment of neutrophils and monocytes to the site of inflammation, and it has been implicated in the development of various inflammatory diseases, including atherosclerosis, rheumatoid arthritis, and inflammatory bowel disease. In addition to its role in inflammation, P-selectin is also involved in the formation of blood clots. It plays a key role in the initial stages of platelet aggregation and the formation of the platelet plug, which is the first step in the process of hemostasis. Overall, P-selectin is an important molecule in the regulation of inflammation and thrombosis, and its dysfunction has been linked to a number of diseases and conditions.
CD18 is a cluster of differentiation antigens that are expressed on the surface of many immune cells, including neutrophils, monocytes, and macrophages. CD18 is a component of the integrin family of cell adhesion molecules, which play a critical role in the recruitment and activation of immune cells at sites of inflammation or infection. Antigens, CD18 are proteins that are recognized by the immune system as foreign or non-self. They are often used as markers to identify and study immune cells, and they can also be targeted by therapeutic agents to modulate immune responses. In the context of infectious diseases, CD18 antigens may be recognized by the immune system as part of the pathogen, leading to the activation and recruitment of immune cells to eliminate the infection.
Inflammation is a complex biological response of the body to harmful stimuli, such as pathogens, damaged cells, or irritants. It is a protective mechanism that helps to eliminate the cause of injury, remove damaged tissue, and initiate the healing process. Inflammation involves the activation of immune cells, such as white blood cells, and the release of chemical mediators, such as cytokines and prostaglandins. This leads to the characteristic signs and symptoms of inflammation, including redness, heat, swelling, pain, and loss of function. Inflammation can be acute or chronic. Acute inflammation is a short-term response that lasts for a few days to a few weeks and is usually beneficial. Chronic inflammation, on the other hand, is a prolonged response that lasts for months or years and can be harmful if it persists. Chronic inflammation is associated with many diseases, including cancer, cardiovascular disease, and autoimmune disorders.
Phagocyte bactericidal dysfunction refers to a condition in which the immune system's phagocytes, which are white blood cells responsible for engulfing and destroying bacteria and other foreign substances, are unable to effectively kill bacteria. This can result in an increased susceptibility to bacterial infections and can be caused by a variety of factors, including genetic mutations, certain medications, and certain medical conditions. Phagocyte bactericidal dysfunction can be diagnosed through blood tests and other diagnostic procedures and can be treated with antibiotics and other medications.
L-Selectin, also known as CD62L, is a type of cell adhesion molecule that plays a crucial role in the immune system. It is expressed on the surface of leukocytes (white blood cells) and is involved in the recruitment of these cells to sites of inflammation or infection. L-Selectin binds to a specific carbohydrate structure called sialyl-Lewisx, which is present on the surface of endothelial cells (the cells that line blood vessels) and other cells. This interaction allows leukocytes to roll along the surface of blood vessels and eventually adhere to the endothelial cells, a process known as leukocyte rolling. Once leukocytes have adhered to the endothelial cells, they can then migrate through the blood vessel wall and into the surrounding tissue, where they can carry out their immune functions. L-Selectin is therefore an important mediator of inflammation and immune cell trafficking, and its dysfunction has been implicated in a number of diseases, including inflammatory bowel disease, multiple sclerosis, and certain types of cancer.
Zymosan is a polysaccharide derived from the cell walls of yeasts and other fungi. It is commonly used in medical research as an activator of the immune system, particularly in the study of inflammation and autoimmune diseases. When zymosan is injected into the body, it triggers an immune response that involves the release of various inflammatory mediators, such as cytokines and chemokines. This response can be used to study the function of immune cells and the signaling pathways involved in inflammation. Zymosan has also been used in clinical trials as a potential treatment for various conditions, including rheumatoid arthritis, psoriasis, and sepsis. However, more research is needed to fully understand its therapeutic potential and potential side effects.
Leukotriene B4 (LTB4) is a biologically active lipid mediator that plays a key role in the inflammatory response. It is produced by leukocytes, particularly neutrophils, in response to various stimuli such as bacterial or fungal infections, tissue damage, or allergic reactions. LTB4 acts as a chemoattractant, recruiting more leukocytes to the site of inflammation and promoting their activation and migration. It also stimulates the release of other pro-inflammatory mediators, such as prostaglandins and cytokines, from leukocytes and other cells. In the medical field, LTB4 is often measured in blood or other body fluids as a marker of inflammation. It is also a target for the development of anti-inflammatory drugs, such as leukotriene receptor antagonists, which block the effects of LTB4 and reduce inflammation.
Intercellular Adhesion Molecule-1 (ICAM-1) is a protein that plays a crucial role in the immune system and cell signaling. It is expressed on the surface of various cell types, including immune cells, endothelial cells, and epithelial cells. ICAM-1 functions as a receptor for immune cells, allowing them to adhere to and migrate across the endothelial cells that line blood vessels. This process is essential for the immune system to respond to infections and other inflammatory stimuli. ICAM-1 also plays a role in cell signaling, mediating the interaction between cells and their environment. It can be activated by various stimuli, including cytokines, hormones, and growth factors, and can regulate processes such as cell proliferation, differentiation, and apoptosis. In the medical field, ICAM-1 is often studied in the context of various diseases, including autoimmune disorders, cancer, and cardiovascular disease. For example, increased expression of ICAM-1 has been associated with the development and progression of several types of cancer, including breast cancer and lung cancer. Additionally, ICAM-1 has been implicated in the pathogenesis of inflammatory diseases such as rheumatoid arthritis and multiple sclerosis.
Cell adhesion molecules (CAMs) are proteins that mediate the attachment of cells to each other or to the extracellular matrix. They play a crucial role in various physiological processes, including tissue development, wound healing, immune response, and cancer progression. There are several types of CAMs, including cadherins, integrins, selectins, and immunoglobulin superfamily members. Each type of CAM has a unique structure and function, and they can interact with other molecules to form complex networks that regulate cell behavior. In the medical field, CAMs are often studied as potential targets for therapeutic interventions. For example, drugs that block specific CAMs have been developed to treat cancer, autoimmune diseases, and cardiovascular disorders. Additionally, CAMs are used as diagnostic markers to identify and monitor various diseases, including cancer, inflammation, and neurodegenerative disorders.
Opsonin proteins are a type of immune system protein that play a role in the process of phagocytosis, which is the process by which immune cells called phagocytes engulf and destroy foreign particles, such as bacteria or viruses. Opsonins bind to the surface of these foreign particles, marking them for destruction by phagocytes. This process is known as opsonization. There are several different types of opsonin proteins, including antibodies, complement proteins, and mannose-binding lectin (MBL). Antibodies are proteins produced by the immune system in response to the presence of a foreign substance, such as a virus or bacteria. They bind to specific molecules on the surface of these foreign particles, marking them for destruction by phagocytes. Complement proteins are a group of proteins that are part of the innate immune system. They are produced by the liver and other organs and circulate in the blood. Complement proteins can bind to foreign particles and mark them for destruction by phagocytes. MBL is a protein that is produced by the liver and circulates in the blood. It binds to specific molecules on the surface of foreign particles, marking them for destruction by phagocytes. Opsonin proteins play an important role in the immune system by helping to identify and destroy foreign particles. They are an important part of the body's defense against infection and disease.
Selectins are a family of cell adhesion molecules that play a crucial role in the recruitment of leukocytes (white blood cells) to sites of inflammation or injury. They are expressed on the surface of endothelial cells (the cells lining blood vessels) and leukocytes, and bind to specific carbohydrate structures on the surface of leukocytes, known as selectin ligands. There are three main selectins: E-selectin, P-selectin, and L-selectin. E-selectin is expressed on the surface of endothelial cells and is upregulated during inflammation, binding to selectin ligands on the surface of rolling leukocytes. P-selectin is expressed on the surface of endothelial cells and platelets, and is involved in the initial adhesion of leukocytes to the blood vessel wall. L-selectin is expressed on the surface of leukocytes and is involved in the rolling of leukocytes along the blood vessel wall. The binding of selectins to their ligands on leukocytes is a critical step in the recruitment of leukocytes to sites of inflammation or injury, and is an important target for the development of anti-inflammatory therapies.
Peroxidase is an enzyme that catalyzes the oxidation of various substrates, including hydrogen peroxide, by transferring an electron from the substrate to molecular oxygen. In the medical field, peroxidase is often used as a diagnostic tool to detect the presence of certain diseases or conditions. One common use of peroxidase is in the detection of cancer. Certain types of cancer cells produce higher levels of peroxidase than normal cells, and this can be detected using peroxidase-based assays. For example, the Papanicolaou (Pap) test, which is used to screen for cervical cancer, relies on the detection of peroxidase activity in cells from the cervix. Peroxidase is also used in the diagnosis of other conditions, such as autoimmune diseases, infections, and liver disease. In these cases, peroxidase activity is often measured in blood or other body fluids, and elevated levels can indicate the presence of a particular disease or condition. Overall, peroxidase is an important tool in the medical field for the diagnosis and monitoring of various diseases and conditions.
Oxyquinoline is a class of organic compounds that are used in the medical field as antiseptics and disinfectants. They are typically used to treat skin infections, such as acne, and to prevent the spread of infections in wounds and burns. Oxyquinoline compounds are also used as preservatives in some topical medications and cosmetics. They work by disrupting the growth of bacteria and other microorganisms on the skin.
Macrophage-1 Antigen (Mac-1) is a protein that is expressed on the surface of certain immune cells, including macrophages and neutrophils. It is also known as CD11b/CD18 or CR3 (complement receptor 3). Mac-1 plays a role in the immune system by mediating the adhesion and migration of immune cells to sites of inflammation or infection. It also plays a role in the recognition and phagocytosis of pathogens by immune cells. In the medical field, Mac-1 is often used as a diagnostic marker for certain diseases, such as sepsis, and as a target for the development of new therapies for inflammatory and infectious diseases.
Arachidonate lipoxygenases (ALOs) are a group of enzymes that catalyze the oxidation of arachidonic acid, a polyunsaturated fatty acid, to produce various eicosanoids. These eicosanoids are signaling molecules that play important roles in regulating inflammation, blood pressure, and other physiological processes. There are several different types of ALOs, including 5-LOX, 12-LOX, and 15-LOX. Each type of ALO produces a different set of eicosanoids, which can have different effects on the body. In the medical field, ALOs and their products are often studied in relation to various diseases and conditions, such as asthma, cardiovascular disease, and cancer. For example, some studies have suggested that elevated levels of certain eicosanoids produced by ALOs may contribute to the development of inflammation and other symptoms associated with these conditions. As a result, drugs that target ALOs or their products are being investigated as potential treatments for these diseases.
In the medical field, superoxides are highly reactive oxygen species that contain one unpaired electron in their outermost shell. They are formed when oxygen molecules (O2) gain an electron and become excited, resulting in the formation of a superoxide radical (O2•-). Superoxides are produced naturally by cells as a byproduct of cellular respiration and are involved in various physiological processes, including the immune response, detoxification, and the regulation of gene expression. However, excessive production of superoxides can also lead to oxidative stress and damage to cellular components, including DNA, proteins, and lipids. In medicine, superoxides are often studied in the context of various diseases, including cancer, cardiovascular disease, and neurodegenerative disorders. They are also used as therapeutic agents in the treatment of certain conditions, such as infections and inflammation.
N-formylmethionine, also known as fMet or formylated methionine, is a modified form of the amino acid methionine. It is a common starting point for the biosynthesis of proteins in bacteria and archaea, and is also found in some eukaryotic organisms. In the medical field, N-formylmethionine is often used as a substrate for the enzyme formyltransferase, which is involved in the biosynthesis of certain types of antibiotics. It is also used as a radiolabeling agent in diagnostic imaging studies, as it can be easily incorporated into proteins and tracked using imaging techniques such as positron emission tomography (PET). In addition, N-formylmethionine has been studied as a potential therapeutic agent for a variety of diseases, including cancer, viral infections, and neurodegenerative disorders. For example, it has been shown to have anti-tumor activity in some cancer cell lines, and may also have neuroprotective effects in models of Parkinson's disease.
E-Selectin is a type of cell adhesion molecule (CAM) that plays a crucial role in the process of inflammation and immune response in the human body. It is a member of the selectin family of proteins, which are involved in the recruitment of leukocytes (white blood cells) to sites of injury or infection. E-Selectin is expressed on the surface of activated endothelial cells (the cells that line the inner surface of blood vessels) and binds to a specific receptor on the surface of leukocytes, known as P-selectin glycoprotein ligand-1 (PSGL-1). This interaction allows the leukocytes to roll along the endothelial cells and eventually adhere to them, a process known as leukocyte rolling. E-Selectin is also involved in the recruitment of platelets to sites of injury, and has been implicated in the development of various inflammatory and cardiovascular diseases, including atherosclerosis, myocardial infarction, and stroke. Therefore, the regulation of E-Selectin expression and function is an important area of research in the medical field.
Arachidonate 5-lipoxygenase (5-LOX) is an enzyme that plays a key role in the metabolism of arachidonic acid, a polyunsaturated fatty acid found in cell membranes. 5-LOX catalyzes the conversion of arachidonic acid to 5-hydroxyeicosatetraenoic acid (5-HETE), which is a precursor to other biologically active molecules such as leukotrienes. Leukotrienes are a group of inflammatory mediators that are involved in the immune response and play a role in the pathogenesis of various diseases, including asthma, allergic reactions, and inflammatory bowel disease. 5-LOX is therefore an important target for the development of anti-inflammatory drugs. In addition to its role in inflammation, 5-LOX has also been implicated in other biological processes, such as platelet aggregation and angiogenesis.
Luminol is a chemical compound that is commonly used in forensic science and medicine to detect the presence of blood or other organic matter. When luminol is mixed with an alkaline solution and exposed to an acidic solution, it emits a blue glow that can be seen in the dark. This property makes luminol useful for detecting blood at crime scenes or in medical settings, where it can be used to identify areas of bleeding or to monitor the effectiveness of treatments for bleeding disorders.
Monoclonal antibodies (mAbs) are laboratory-made proteins that can mimic the immune system's ability to fight off harmful pathogens, such as viruses and bacteria. They are produced by genetically engineering cells to produce large quantities of a single type of antibody, which is specific to a particular antigen (a molecule that triggers an immune response). In the medical field, monoclonal antibodies are used to treat a variety of conditions, including cancer, autoimmune diseases, and infectious diseases. They can be administered intravenously, intramuscularly, or subcutaneously, depending on the condition being treated. Monoclonal antibodies work by binding to specific antigens on the surface of cells or pathogens, marking them for destruction by the immune system. They can also block the activity of specific molecules involved in disease processes, such as enzymes or receptors. Overall, monoclonal antibodies have revolutionized the treatment of many diseases, offering targeted and effective therapies with fewer side effects than traditional treatments.
Chemokines are a family of small signaling proteins that play a crucial role in the immune system. They are produced by various cells in response to infection, injury, or inflammation and act as chemical messengers to attract immune cells to the site of injury or infection. Chemokines bind to specific receptors on the surface of immune cells, such as neutrophils, monocytes, and lymphocytes, and guide them to the site of infection or injury. They also play a role in regulating the migration and activation of immune cells within tissues. In the medical field, chemokines are important for understanding and treating various diseases, including cancer, autoimmune disorders, and infectious diseases. They are also being studied as potential therapeutic targets for the development of new drugs to treat these conditions.
Cytokines are small proteins that are produced by various cells of the immune system, including white blood cells, macrophages, and dendritic cells. They play a crucial role in regulating immune responses and inflammation, and are involved in a wide range of physiological processes, including cell growth, differentiation, and apoptosis. Cytokines can be classified into different groups based on their function, including pro-inflammatory cytokines, anti-inflammatory cytokines, and regulatory cytokines. Pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 (IL-1), promote inflammation and recruit immune cells to the site of infection or injury. Anti-inflammatory cytokines, such as interleukin-10 (IL-10) and transforming growth factor-beta (TGF-beta), help to dampen the immune response and prevent excessive inflammation. Regulatory cytokines, such as interleukin-4 (IL-4) and interleukin-13 (IL-13), help to regulate the balance between pro-inflammatory and anti-inflammatory responses. Cytokines play a critical role in many diseases, including autoimmune disorders, cancer, and infectious diseases. They are also important in the development of vaccines and immunotherapies.
Tumor Necrosis Factor-alpha (TNF-alpha) is a cytokine, a type of signaling protein, that plays a crucial role in the immune response and inflammation. It is produced by various cells in the body, including macrophages, monocytes, and T cells, in response to infection, injury, or other stimuli. TNF-alpha has multiple functions in the body, including regulating the immune response, promoting cell growth and differentiation, and mediating inflammation. It can also induce programmed cell death, or apoptosis, in some cells, which can be beneficial in fighting cancer. However, excessive or prolonged TNF-alpha production can lead to chronic inflammation and tissue damage, which can contribute to the development of various diseases, including autoimmune disorders, inflammatory bowel disease, and certain types of cancer. In the medical field, TNF-alpha is often targeted in the treatment of these conditions. For example, drugs called TNF inhibitors, such as infliximab and adalimumab, are used to block the action of TNF-alpha and reduce inflammation in patients with rheumatoid arthritis, Crohn's disease, and other inflammatory conditions.
In the medical field, RNA, Messenger (mRNA) refers to a type of RNA molecule that carries genetic information from DNA in the nucleus of a cell to the ribosomes, where proteins are synthesized. During the process of transcription, the DNA sequence of a gene is copied into a complementary RNA sequence called messenger RNA (mRNA). This mRNA molecule then leaves the nucleus and travels to the cytoplasm of the cell, where it binds to ribosomes and serves as a template for the synthesis of a specific protein. The sequence of nucleotides in the mRNA molecule determines the sequence of amino acids in the protein that is synthesized. Therefore, changes in the sequence of nucleotides in the mRNA molecule can result in changes in the amino acid sequence of the protein, which can affect the function of the protein and potentially lead to disease. mRNA molecules are often used in medical research and therapy as a way to introduce new genetic information into cells. For example, mRNA vaccines work by introducing a small piece of mRNA that encodes for a specific protein, which triggers an immune response in the body.
Lipopolysaccharides (LPS) are a type of complex carbohydrate found on the surface of gram-negative bacteria. They are composed of a lipid A moiety, a core polysaccharide, and an O-specific polysaccharide. LPS are important components of the bacterial cell wall and play a role in the innate immune response of the host. In the medical field, LPS are often studied in the context of sepsis, a life-threatening condition that occurs when the body's response to an infection causes widespread inflammation. LPS can trigger a strong immune response in the host, leading to the release of pro-inflammatory cytokines and other mediators that can cause tissue damage and organ failure. As a result, LPS are often used as a model for studying the pathophysiology of sepsis and for developing new treatments for this condition. LPS are also used in research as a tool for studying the immune system and for developing vaccines against bacterial infections. They can be purified from bacterial cultures and used to stimulate immune cells in vitro or in animal models, allowing researchers to study the mechanisms of immune responses to bacterial pathogens. Additionally, LPS can be used as an adjuvant in vaccines to enhance the immune response to the vaccine antigen.
Complement C5a is a protein that is produced as a result of the activation of the complement system, which is a part of the immune system. The complement system is a series of proteins that work together to help the body fight off infections and other foreign substances. Complement C5a is a potent inflammatory mediator that is involved in the recruitment of immune cells to the site of infection or injury. It does this by binding to receptors on the surface of immune cells, such as neutrophils and macrophages, and triggering a signaling cascade that leads to the release of these cells from the blood vessels and their migration to the site of inflammation. Complement C5a also has other functions, such as promoting the activation of the complement system and enhancing the ability of immune cells to phagocytose (engulf and destroy) pathogens. In the medical field, complement C5a is often measured as a marker of inflammation and immune system activation. It is also being studied as a potential therapeutic target for a variety of conditions, including autoimmune diseases, infections, and cancer.
Interleukin-8 (IL-8) is a type of cytokine, which is a signaling molecule that plays a role in regulating the immune system. It is produced by various types of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. IL-8 is primarily involved in the recruitment and activation of neutrophils, which are a type of white blood cell that plays a key role in the body's defense against infection and inflammation. IL-8 binds to receptors on the surface of neutrophils, causing them to migrate to the site of infection or inflammation. It also promotes the production of other pro-inflammatory molecules by neutrophils, which helps to amplify the immune response. IL-8 has been implicated in a variety of inflammatory and autoimmune diseases, including chronic obstructive pulmonary disease (COPD), asthma, rheumatoid arthritis, and inflammatory bowel disease. It is also involved in the development of certain types of cancer, such as lung cancer and ovarian cancer. In the medical field, IL-8 is often measured in blood or other bodily fluids as a marker of inflammation or immune activation. It is also being studied as a potential therapeutic target for the treatment of various diseases, including cancer and inflammatory disorders.
Indium is a chemical element with the symbol In and atomic number 49. It is a soft, silvery-white metal that is not commonly used in the medical field. However, indium compounds have been studied for their potential medical applications. One potential use of indium compounds in medicine is as imaging agents for diagnostic imaging. Indium-111, a radioactive isotope of indium, has been used in nuclear medicine to image tumors, infections, and other abnormalities in the body. It is often used in conjunction with a radiolabeled antibody or other targeting molecule to specifically target and image certain cells or tissues. Indium compounds have also been studied for their potential use in treating cancer. For example, indium-111-labeled monoclonal antibodies have been used in clinical trials to treat certain types of cancer, such as non-Hodgkin's lymphoma and breast cancer. In addition, indium compounds have been studied for their potential use in treating other medical conditions, such as Alzheimer's disease and diabetes. However, more research is needed to fully understand the potential benefits and risks of using indium compounds in medicine.
In the medical field, "Disease Models, Animal" refers to the use of animals to study and understand human diseases. These models are created by introducing a disease or condition into an animal, either naturally or through experimental manipulation, in order to study its progression, symptoms, and potential treatments. Animal models are used in medical research because they allow scientists to study diseases in a controlled environment and to test potential treatments before they are tested in humans. They can also provide insights into the underlying mechanisms of a disease and help to identify new therapeutic targets. There are many different types of animal models used in medical research, including mice, rats, rabbits, dogs, and monkeys. Each type of animal has its own advantages and disadvantages, and the choice of model depends on the specific disease being studied and the research question being addressed.
Platelet Activating Factor (PAF) is a signaling molecule that plays a role in the immune response and inflammation. It is produced by various cells, including platelets, leukocytes, and endothelial cells, and acts on a specific receptor on the surface of these cells to trigger a variety of cellular responses. PAF is involved in the recruitment and activation of immune cells, such as neutrophils and monocytes, to sites of inflammation. It also promotes the release of other inflammatory mediators, such as prostaglandins and leukotrienes, and can cause vasodilation and increased permeability of blood vessels, leading to edema and tissue damage. In addition to its role in inflammation, PAF has been implicated in a variety of other conditions, including allergic reactions, asthma, and certain types of heart disease. It is also a potential therapeutic target for the treatment of these conditions.
Complement C5 is a protein that plays a crucial role in the immune system's response to infections and inflammation. It is one of the proteins in the complement system, a group of proteins that work together to help the immune system identify and destroy invading pathogens. Complement C5 is produced by immune cells and is activated when it comes into contact with the surface of a pathogen. Once activated, it cleaves into two fragments, C5a and C5b, which then trigger a series of reactions that lead to the destruction of the pathogen. C5a is a potent inflammatory mediator that attracts immune cells to the site of infection and stimulates the release of other inflammatory molecules. C5b, on the other hand, is a key component of the membrane attack complex (MAC), which forms a pore in the membrane of the pathogen, leading to its destruction. Complement C5 is also involved in other immune processes, such as the clearance of immune complexes from the bloodstream and the regulation of inflammation. Deficiencies in complement C5 can lead to increased susceptibility to infections and autoimmune diseases.
Nitroblue Tetrazolium (NBT) is a chemical compound that is commonly used in medical research and diagnostics. It is a diazo dye that is reduced to a formazan product when it comes into contact with certain enzymes, such as superoxide dismutase (SOD), which is an antioxidant enzyme found in many cells. In medical research, NBT is often used as a colorimetric assay to measure the activity of SOD in cells or tissues. The reduction of NBT to formazan is a color change that can be easily detected and quantified using a spectrophotometer or other colorimetric methods. In addition to its use as a research tool, NBT has also been used in clinical diagnostics to detect certain types of infections and inflammatory conditions. For example, the presence of certain bacteria or white blood cells can cause an increase in SOD activity, which can be detected using NBT assays. Overall, NBT is a useful tool in medical research and diagnostics due to its ability to detect and quantify the activity of SOD, which is an important enzyme involved in many cellular processes.
Vascular Cell Adhesion Molecule-1 (VCAM-1) is a protein that plays a crucial role in the immune system's response to inflammation and infection. It is expressed on the surface of endothelial cells, which line the inner lining of blood vessels, and is involved in the recruitment of immune cells, such as monocytes and T cells, to sites of inflammation. VCAM-1 binds to a protein called integrin on the surface of immune cells, which triggers a series of signaling events that lead to the adhesion of the immune cells to the endothelial cells. This process is essential for the immune system to mount an effective response to infection or injury, but it can also contribute to the development of chronic inflammation and autoimmune diseases. In addition to its role in immune cell recruitment, VCAM-1 has been implicated in the development of a variety of cardiovascular diseases, including atherosclerosis, hypertension, and heart failure. It is also involved in the progression of certain types of cancer, such as breast and colon cancer. Overall, VCAM-1 is a key player in the complex interplay between the immune system and the vasculature, and its dysregulation has been linked to a range of diseases and conditions.
Leukotriene A4 (LTA4) is a chemical compound that is produced by leukocytes (white blood cells) in response to inflammation. It is a precursor to other leukotrienes, which are signaling molecules that play a role in regulating immune responses and inflammation. LTA4 is synthesized from arachidonic acid, a fatty acid that is released from cell membranes in response to injury or infection. The enzyme 5-lipoxygenase (5-LOX) catalyzes the conversion of arachidonic acid to LTA4. LTA4 has several effects on the body, including: 1. Contraction of smooth muscle cells in the airways, leading to bronchoconstriction and difficulty breathing. 2. Increased production of mucus in the airways, which can lead to coughing and difficulty breathing. 3. Increased blood vessel permeability, which can lead to swelling and inflammation. 4. Increased production of other leukotrienes, which can amplify the inflammatory response. LTA4 is involved in several inflammatory diseases, including asthma, allergic reactions, and inflammatory bowel disease. Inhibitors of 5-LOX, which block the production of LTA4, are used as medications to treat these conditions.
Lymphocyte Function-Associated Antigen-1 (LFA-1) is a protein found on the surface of white blood cells, particularly lymphocytes. It plays a crucial role in the immune system by mediating the adhesion of immune cells to other cells and to the extracellular matrix. LFA-1 binds to a protein called intercellular adhesion molecule-1 (ICAM-1) on the surface of other cells, allowing immune cells to migrate to sites of infection or inflammation. LFA-1 is also involved in the activation of immune cells, and its function is regulated by various signaling pathways. Disruptions in LFA-1 function have been implicated in a number of autoimmune and inflammatory diseases.
Peritonitis is a medical condition characterized by the inflammation of the peritoneum, which is the thin, flexible membrane that lines the inside of the abdominal cavity. The peritoneum plays an important role in protecting the abdominal organs and helping to move them around the body. Peritonitis can be caused by a variety of factors, including bacterial infections, viral infections, parasitic infections, and physical injury to the peritoneum. It can also be caused by the spread of infection from another part of the body, such as the urinary tract or the reproductive system. Symptoms of peritonitis can include abdominal pain, fever, nausea and vomiting, abdominal tenderness, and a low-grade fever. In severe cases, peritonitis can lead to sepsis, a life-threatening condition characterized by widespread inflammation throughout the body. Treatment for peritonitis typically involves antibiotics to treat the underlying infection, as well as supportive care to manage symptoms and prevent complications. In some cases, surgery may be necessary to remove infected tissue or drain fluid from the abdomen.
Blood proteins are proteins that are found in the blood plasma of humans and other animals. They play a variety of important roles in the body, including transporting oxygen and nutrients, regulating blood pressure, and fighting infections. There are several different types of blood proteins, including albumin, globulins, and fibrinogen. Each type of blood protein has a specific function and is produced by different cells in the body. For example, albumin is produced by the liver and helps to maintain the osmotic pressure of the blood, while globulins are produced by the immune system and help to fight infections. Fibrinogen, on the other hand, is produced by the liver and is involved in the clotting of blood.
Receptors, Chemokine are proteins found on the surface of cells that bind to specific chemokines, which are small signaling molecules that play a role in immune cell trafficking and inflammation. These receptors are involved in the regulation of immune cell migration and are important for the recruitment of immune cells to sites of infection or injury. There are several different types of chemokine receptors, each of which is specific to a particular chemokine or group of chemokines. Dysregulation of chemokine receptors has been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases.
Leukocytosis is a medical condition characterized by an abnormally high number of white blood cells (leukocytes) in the blood. The normal range of white blood cells in the blood is typically between 4,000 and 11,000 cells per microliter (µL) of blood. When the number of white blood cells exceeds this range, it is considered leukocytosis. Leukocytosis can be caused by a variety of factors, including infections, inflammation, stress, and certain medications. In some cases, leukocytosis may be a normal response to an infection or injury, but in other cases, it may be a sign of a more serious underlying condition. Leukocytosis can be classified into two types: absolute leukocytosis and relative leukocytosis. Absolute leukocytosis refers to an increase in the actual number of white blood cells in the blood, while relative leukocytosis refers to an increase in the proportion of white blood cells in the blood compared to other types of blood cells. Leukocytosis can be detected through a complete blood count (CBC) test, which measures the number and types of cells in the blood. Treatment for leukocytosis depends on the underlying cause and may include antibiotics, anti-inflammatory medications, or other therapies.
Peroxidases are a group of enzymes that catalyze the oxidation of various substrates using hydrogen peroxide as the oxidizing agent. In the medical field, peroxidases are commonly used as diagnostic tools to detect the presence of specific substances in biological samples, such as blood, urine, or tissue. One of the most well-known peroxidases in medicine is the enzyme lactoperoxidase, which is found in high concentrations in human milk. Lactoperoxidase plays a crucial role in protecting the newborn from bacterial and viral infections by generating antimicrobial compounds. Another important peroxidase in medicine is the enzyme myeloperoxidase, which is produced by white blood cells (neutrophils) and is involved in the immune response against infections. Myeloperoxidase is often used as a marker of inflammation in various medical conditions, such as chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, and inflammatory bowel disease. Peroxidases are also used in forensic science to analyze biological samples for evidence in criminal investigations. For example, the enzyme cytochrome c peroxidase can be used to detect the presence of blood at a crime scene, while the enzyme glucose oxidase is used to detect the presence of glucose in urine samples.
Leukotrienes are a group of biologically active molecules that are produced by leukocytes (white blood cells) in response to inflammation. They are synthesized from arachidonic acid, which is an essential fatty acid found in cell membranes. There are several different types of leukotrienes, including leukotriene A4 (LTA4), leukotriene B4 (LTB4), leukotriene C4 (LTC4), leukotriene D4 (LTD4), and leukotriene E4 (LTE4). These molecules have a variety of effects on the body, including: 1. Constricting blood vessels: Leukotrienes can cause blood vessels to narrow, which can increase blood pressure and contribute to inflammation. 2. Recruiting immune cells: Leukotrienes can attract immune cells to the site of inflammation, which can help to fight off infections. 3. Increasing mucus production: Leukotrienes can stimulate the production of mucus in the respiratory tract, which can lead to symptoms such as coughing and wheezing. 4. Aggravating allergic reactions: Leukotrienes can worsen allergic reactions by increasing inflammation and mucus production. Leukotrienes are involved in a number of different medical conditions, including asthma, allergic rhinitis, and chronic obstructive pulmonary disease (COPD). They are also involved in the development of certain types of cancer, such as lung cancer and colon cancer. Medications that block the production or action of leukotrienes are used to treat these conditions.
Receptors, Formyl Peptide are a type of protein receptors found on the surface of immune cells, such as neutrophils and macrophages. These receptors are activated by the presence of formylated peptides, which are a type of amino acid sequence found on the N-terminus of certain bacterial proteins. Activation of these receptors triggers a signaling cascade that leads to the recruitment and activation of immune cells at the site of infection, helping to mount an immune response against the invading bacteria.
Granulomatous disease is a type of chronic inflammatory condition characterized by the formation of granulomas, which are collections of immune cells, including macrophages, lymphocytes, and giant cells, that form around foreign substances or damaged tissue. Chronic granulomatous disease refers specifically to a group of rare genetic disorders that affect the immune system's ability to fight off certain types of bacteria and fungi. These disorders are caused by mutations in genes that are involved in the production of enzymes that are necessary for the proper functioning of phagocytes, which are immune cells that engulf and destroy foreign substances. Chronic granulomatous disease can manifest in a variety of ways, depending on the specific gene mutation involved. Some common symptoms include recurrent infections, particularly with certain types of bacteria and fungi, as well as skin rashes, fever, and fatigue. Treatment typically involves antibiotics and other medications to manage symptoms and prevent infections. In some cases, bone marrow transplantation may be necessary to replace damaged immune cells.
Arachidonic acid (AA) is a polyunsaturated omega-6 fatty acid that is found in the cell membranes of all living organisms. It is an essential fatty acid, meaning that it cannot be synthesized by the body and must be obtained through the diet. In the medical field, arachidonic acid is known for its role in the production of eicosanoids, a group of signaling molecules that play important roles in various physiological processes, including inflammation, blood clotting, and immune function. Eicosanoids are synthesized from arachidonic acid by enzymes called cyclooxygenases (COXs) and lipoxygenases (LOXs). Arachidonic acid is also a precursor to the synthesis of prostaglandins, which are another group of eicosanoids that have a wide range of effects on the body, including regulating blood pressure, controlling inflammation, and modulating pain and fever. In addition to its role in eicosanoid production, arachidonic acid is also important for maintaining the fluidity and integrity of cell membranes, and for regulating the activity of various enzymes and signaling molecules. Abnormal levels of arachidonic acid or disruptions in its metabolism have been linked to a number of medical conditions, including cardiovascular disease, inflammatory disorders, and neurological disorders. As a result, arachidonic acid is an important area of research in the medical field, with efforts focused on developing new treatments and therapies for these conditions.
Pancreatic elastase is a digestive enzyme that is produced by the pancreas and is responsible for breaking down proteins in the small intestine. It is a serine protease that cleaves peptide bonds in proteins, particularly those that contain the amino acids arginine and lysine. Pancreatic elastase is secreted by the pancreas into the small intestine, where it helps to break down dietary proteins into smaller peptides and amino acids that can be absorbed by the body. It also plays a role in the breakdown of certain hormones and other proteins in the body. Abnormalities in the production or function of pancreatic elastase can lead to a variety of digestive disorders, including chronic pancreatitis, cystic fibrosis, and certain types of cancer. In these conditions, the pancreas may not produce enough elastase, or the enzyme may not function properly, leading to malabsorption of nutrients and other digestive problems.
Membrane glycoproteins are proteins that are attached to the cell membrane through a glycosyl group, which is a complex carbohydrate. These proteins play important roles in cell signaling, cell adhesion, and cell recognition. They are involved in a wide range of biological processes, including immune response, cell growth and differentiation, and nerve transmission. Membrane glycoproteins can be classified into two main types: transmembrane glycoproteins, which span the entire cell membrane, and peripheral glycoproteins, which are located on one side of the membrane.
Muramidase is an enzyme that is involved in the degradation of peptidoglycan, a major component of bacterial cell walls. It is also known as lysozyme or muramidase lysozyme. The enzyme cleaves the bond between the N-acetylglucosamine and N-acetylmuramic acid residues in the peptidoglycan chain, leading to the breakdown of the cell wall and ultimately the death of the bacterium. Muramidase is found in various organisms, including humans, and is used as an antimicrobial agent in some medications. It is also used in laboratory research to study bacterial cell wall structure and function.
Chediak-Higashi Syndrome (CHS) is a rare, inherited disorder that affects the immune system and causes a variety of symptoms. It is caused by mutations in the CHS1 gene, which is responsible for producing a protein called LYST that is involved in the functioning of lysosomes, organelles in cells that help break down and recycle waste materials. In CHS, the LYST protein is not functioning properly, leading to the accumulation of large, abnormal lysosomes in various cells throughout the body. This can cause a range of symptoms, including recurrent infections, bleeding disorders, and neurological problems. Some of the specific symptoms of CHS can include: - Recurrent infections, particularly of the respiratory tract, skin, and gastrointestinal tract - Easy bruising and bleeding - Abnormal pigmentation of the skin and mucous membranes - Enlarged lymph nodes - Swelling of the tongue and tonsils - Seizures and other neurological problems - Developmental delays and intellectual disability in some cases CHS is a very rare disorder, with only a few hundred cases reported worldwide. It is typically diagnosed in childhood, and treatment is focused on managing the symptoms and preventing infections. There is currently no cure for CHS.
Tetradecanoylphorbol acetate (TPA) is a synthetic compound that belongs to a class of chemicals called phorbol esters. It is a potent tumor promoter and has been used in research to study the mechanisms of cancer development and progression. TPA works by activating protein kinase C (PKC), a family of enzymes that play a key role in cell signaling and proliferation. When TPA binds to a specific receptor on the cell surface, it triggers a cascade of events that leads to the activation of PKC, which in turn promotes cell growth and division. TPA has been shown to promote the growth of tumors in animal models and has been linked to the development of certain types of cancer in humans, including skin cancer and breast cancer. It is also used in some experimental treatments for cancer, although its use is limited due to its potential toxicity and side effects.
Hydrogen peroxide (H2O2) is a colorless, odorless liquid that is commonly used in the medical field as a disinfectant, antiseptic, and oxidizing agent. It is a strong oxidizing agent that can break down organic matter, including bacteria, viruses, and fungi, making it useful for disinfecting wounds, surfaces, and medical equipment. In addition to its disinfectant properties, hydrogen peroxide is also used in wound care to remove dead tissue and promote healing. It is often used in combination with other wound care products, such as saline solution or antibiotic ointment, to help prevent infection and promote healing. Hydrogen peroxide is also used in some medical procedures, such as endoscopy and bronchoscopy, to help clean and disinfect the equipment before use. It is also used in some dental procedures to help remove stains and whiten teeth. However, it is important to note that hydrogen peroxide can be harmful if not used properly. It should not be ingested or applied directly to the skin or mucous membranes without first diluting it with water. It should also be stored in a cool, dry place away from children and pets.
Chemokine CCL2, also known as monocyte chemoattractant protein-1 (MCP-1), is a small protein that plays a crucial role in the immune system. It is a member of the chemokine family of proteins, which are responsible for regulating the movement of immune cells within the body. CCL2 is primarily produced by cells such as monocytes, macrophages, and endothelial cells in response to inflammatory stimuli. It functions as a chemoattractant, drawing immune cells towards the site of inflammation or infection. Specifically, CCL2 attracts monocytes and T cells to the site of injury or infection, where they can help to clear the infection and promote tissue repair. In addition to its role in immune cell recruitment, CCL2 has also been implicated in a variety of other physiological processes, including angiogenesis (the formation of new blood vessels), tissue repair, and cancer progression. Dysregulation of CCL2 expression or function has been linked to a number of diseases, including atherosclerosis, diabetes, and certain types of cancer.
Hydroxyeicosatetraenoic acids (HETEs) are a group of bioactive lipids that are derived from the metabolism of arachidonic acid (AA) by enzymes called lipoxygenases. HETEs are involved in various physiological processes, including inflammation, blood pressure regulation, and blood clotting. There are several different HETEs, including 5-hydroxyeicosatetraenoic acid (5-HETE), 12-hydroxyeicosatetraenoic acid (12-HETE), and 15-hydroxyeicosatetraenoic acid (15-HETE). These compounds are produced by the action of lipoxygenases on AA, which is a polyunsaturated fatty acid that is abundant in cell membranes. HETEs can act as signaling molecules, binding to specific receptors on the surface of cells and triggering a variety of cellular responses. For example, 5-HETE has been shown to promote the proliferation of smooth muscle cells, which can contribute to the development of atherosclerosis. 12-HETE has been implicated in the regulation of blood pressure, while 15-HETE has been linked to the formation of blood clots. Overall, HETEs play important roles in many physiological processes, and their dysregulation has been implicated in a variety of diseases, including cardiovascular disease, cancer, and inflammatory disorders.
Interleukin-1 (IL-1) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. IL-1 is produced by various types of immune cells, including macrophages, monocytes, and dendritic cells, in response to infection, injury, or inflammation. IL-1 has multiple functions in the immune system, including promoting the activation and proliferation of immune cells, enhancing the production of other cytokines, and regulating the inflammatory response. It can also stimulate the production of fever, which helps to fight off infections. In the medical field, IL-1 is often studied in the context of various diseases, including autoimmune disorders, inflammatory bowel disease, and rheumatoid arthritis. It is also being investigated as a potential target for the development of new treatments for these conditions.
Cytochalasin B is a fungal metabolite that is used in the medical field as a research tool to study cell biology and cell motility. It is a potent inhibitor of actin polymerization, which is a key process in cell movement and division. Cytochalasin B is often used to study the dynamics of actin filaments and their role in cell migration, endocytosis, and cytokinesis. It is also used to study the effects of actin polymerization on the structure and function of other cellular components, such as microtubules and membrane proteins. In addition, cytochalasin B has been used in the treatment of certain types of cancer, as it can inhibit the growth and spread of cancer cells by disrupting their actin cytoskeleton.
Integrin alpha4 is a protein that plays a crucial role in the immune system and is involved in the adhesion of immune cells to the blood vessels and tissues. It is a member of the integrin family of proteins, which are transmembrane receptors that mediate cell-cell and cell-extracellular matrix interactions. In the medical field, integrin alpha4 is often studied in the context of autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis, where it is thought to play a role in the migration of immune cells into the central nervous system and the joints, respectively. It is also involved in the development and function of various immune cells, including T cells, B cells, and dendritic cells. Integrin alpha4 is also a target for therapeutic intervention in certain diseases. For example, monoclonal antibodies that block the interaction between integrin alpha4 and its ligand, VCAM-1, have been developed for the treatment of multiple sclerosis and other autoimmune diseases.
Glucuronidase is an enzyme that breaks down glucuronides, which are conjugated forms of various substances, including drugs, hormones, and toxins. In the medical field, glucuronidase is often used as a diagnostic tool to detect the presence of specific substances in the body. For example, in the field of forensic toxicology, glucuronidase can be used to detect the presence of drugs such as cocaine, amphetamines, and opioids in biological samples, such as urine or blood. This is because these drugs are often metabolized in the body by conjugation with glucuronic acid, forming glucuronides. By measuring the levels of glucuronides in a sample, forensic toxicologists can determine whether a person has recently used these drugs. In addition to its use in forensic toxicology, glucuronidase is also used in the treatment of certain medical conditions. For example, in the treatment of certain types of cancer, glucuronidase can be used to break down conjugated toxins that have accumulated in the body, potentially reducing their toxicity and improving patient outcomes.
Lactoferrin is a glycoprotein that is found in high concentrations in the milk of mammals, including humans. It is also present in other bodily fluids, such as tears, saliva, and mucous secretions. Lactoferrin has a number of biological functions, including: 1. Immune system support: Lactoferrin has antimicrobial properties and can help to protect against bacterial, viral, and fungal infections. It also has anti-inflammatory effects and can help to modulate the immune response. 2. Iron metabolism: Lactoferrin binds to iron and helps to regulate its absorption and distribution in the body. This can help to prevent iron deficiency anemia. 3. Growth and development: Lactoferrin is important for the growth and development of infants, as it is a major source of iron and other nutrients in breast milk. 4. Anti-cancer effects: Some studies have suggested that lactoferrin may have anti-cancer properties, although more research is needed to confirm this. Lactoferrin is sometimes used as a dietary supplement, particularly in the form of lactoferrin-rich milk products or as a powder that can be mixed into food or drinks. It is also used in some medical treatments, such as the treatment of iron deficiency anemia and certain infections.
Lipoxins are a class of bioactive lipids that are produced by leukocytes (white blood cells) in response to inflammation. They are synthesized from arachidonic acid, which is an omega-6 fatty acid found in cell membranes. Lipoxins have anti-inflammatory properties and play a role in resolving inflammation. They can inhibit the production of pro-inflammatory cytokines and chemokines, reduce the recruitment of immune cells to the site of inflammation, and promote the clearance of apoptotic cells. Lipoxins have been implicated in a variety of inflammatory conditions, including asthma, chronic obstructive pulmonary disease (COPD), rheumatoid arthritis, and cardiovascular disease. They have also been shown to have potential therapeutic applications in these conditions. Overall, lipoxins are an important class of molecules that play a critical role in regulating inflammation and promoting tissue repair.
Leukopenia is a medical condition characterized by a low number of white blood cells (leukocytes) in the blood. The normal range of white blood cells in the blood is typically between 4,500 and 11,000 cells per microliter (µL) of blood. When the number of white blood cells falls below 4,000 cells/µL, it is considered leukopenia. Leukopenia can be caused by a variety of factors, including infections, autoimmune disorders, certain medications, radiation therapy, chemotherapy, and bone marrow disorders. It can also be a symptom of more serious underlying conditions, such as leukemia, lymphoma, or other blood disorders. Symptoms of leukopenia may include fatigue, weakness, fever, chills, and an increased susceptibility to infections. Treatment for leukopenia depends on the underlying cause and may include medications to stimulate the production of white blood cells, antibiotics to treat infections, or other therapies to address the underlying condition.
The complement system is a complex network of proteins that plays a crucial role in the immune system's defense against infections. Complement system proteins are a group of proteins that are produced by the liver and other cells in the body and circulate in the blood. These proteins work together to identify and destroy invading pathogens, such as bacteria and viruses, by forming a membrane attack complex (MAC) that punctures the pathogen's cell membrane, causing it to burst and die. There are several different types of complement system proteins, including: 1. Complement proteins: These are the primary components of the complement system and include C1, C2, C3, C4, C5, C6, C7, C8, and C9. 2. Complement regulatory proteins: These proteins help to control the activation of the complement system and prevent it from attacking healthy cells. Examples include C1 inhibitor, C4 binding protein, and decay-accelerating factor. 3. Complement receptors: These proteins are found on the surface of immune cells and help to bind to and activate complement proteins. Examples include CR1, CR2, and CR3. Complement system proteins play a critical role in the immune response and are involved in a wide range of diseases, including autoimmune disorders, infections, and cancer.
CD31 is a protein that is expressed on the surface of certain cells in the immune system, including platelets and certain types of white blood cells. It is also known as platelet endothelial cell adhesion molecule-1 (PECAM-1) or cluster of differentiation 31 (CD31). In the medical field, CD31 is often used as a marker to identify and study certain types of cells, particularly those involved in the immune response. It is also used as a diagnostic tool to help diagnose and monitor certain medical conditions, such as cancer and cardiovascular disease. CD31 is also used in research to study the function of immune cells and to develop new treatments for various diseases. For example, it has been shown to play a role in the formation of new blood vessels, which is important for wound healing and tissue repair. It is also involved in the regulation of the immune response and the development of certain types of cancer.
Calcimycin, also known as FK506, is a medication that belongs to a class of drugs called immunosuppressants. It is primarily used to prevent organ rejection in people who have received a transplant, such as a kidney or liver transplant. Calcimycin works by inhibiting the activity of a protein called calcineurin, which plays a key role in the activation of T-cells, a type of white blood cell that is involved in the immune response. By inhibiting calcineurin, calcimycin helps to suppress the immune system and reduce the risk of organ rejection. Calcimycin is usually given as an oral tablet or as an injection. It can cause side effects such as headache, nausea, and diarrhea, and it may interact with other medications.
Chemokines, CXC are a family of small proteins that play a crucial role in the immune system. They are secreted by various cells in response to infection, injury, or inflammation and act as chemoattractants to recruit immune cells to the site of injury or infection. CXC chemokines are characterized by the presence of a conserved cysteine (C) at the first position and a glutamine (Q) or glutamic acid (E) at the second position in their amino acid sequence. They are classified into four subfamilies based on the position of the second cysteine residue: CX3C, CXCL, CXCL1, and CXCL2. CXC chemokines play a critical role in the recruitment and activation of immune cells, including neutrophils, monocytes, and lymphocytes, to the site of infection or injury. They also play a role in the development of chronic inflammatory diseases, such as asthma, rheumatoid arthritis, and atherosclerosis. In the medical field, CXC chemokines are used as diagnostic markers for various diseases, including cancer, infectious diseases, and autoimmune disorders. They are also being investigated as potential therapeutic targets for the treatment of these diseases.
CD11b is a type of protein found on the surface of certain immune cells, such as neutrophils and monocytes. It is a member of the integrin family of proteins, which are involved in cell adhesion and signaling. CD11b is also known as the alpha chain of the integrin receptor Mac-1 (Macrophage-1 antigen). Antigens, CD11b are molecules that bind to CD11b on the surface of immune cells. These antigens can be foreign substances, such as bacteria or viruses, or they can be self-molecules that have been altered in some way. When CD11b binds to an antigen, it triggers a series of signaling events that activate the immune cell and cause it to respond to the presence of the antigen. This response can include the production of inflammatory molecules, the recruitment of other immune cells to the site of the antigen, and the destruction of the antigen. CD11b and its antigens play an important role in the immune response and are the subject of ongoing research in the field of immunology.
Receptors, Leukocyte-Adhesion are proteins found on the surface of white blood cells (leukocytes) that allow them to adhere to and migrate to sites of inflammation or infection. These receptors recognize specific molecules on the surface of other cells or the extracellular matrix, and bind to them, leading to the activation of intracellular signaling pathways that promote adhesion and migration. The most well-known leukocyte-adhesion receptors are the integrins, which are heterodimeric transmembrane proteins that mediate cell-cell and cell-extracellular matrix interactions. Other leukocyte-adhesion receptors include selectins, which are involved in the rolling of leukocytes along the endothelium, and chemokine receptors, which are activated by chemokines and promote leukocyte migration towards the site of inflammation or infection.
Hexosephosphates are a group of compounds that consist of a hexose sugar (such as glucose, fructose, or galactose) attached to a phosphate group. In the medical field, hexosephosphates are often used as markers for certain diseases or conditions, such as diabetes or liver disease. They can also be used as diagnostic tools to help identify and monitor certain types of cancer, such as osteosarcoma or Ewing's sarcoma. Hexosephosphates are produced by the body as a result of certain metabolic processes, and their levels in the blood can provide important information about a person's overall health and well-being.
Recombinant proteins are proteins that are produced by genetically engineering bacteria, yeast, or other organisms to express a specific gene. These proteins are typically used in medical research and drug development because they can be produced in large quantities and are often more pure and consistent than proteins that are extracted from natural sources. Recombinant proteins can be used for a variety of purposes in medicine, including as diagnostic tools, therapeutic agents, and research tools. For example, recombinant versions of human proteins such as insulin, growth hormones, and clotting factors are used to treat a variety of medical conditions. Recombinant proteins can also be used to study the function of specific genes and proteins, which can help researchers understand the underlying causes of diseases and develop new treatments.
CD45 is a type of protein found on the surface of many different types of immune cells, including white blood cells. It is also known as leukocyte common antigen or lymphocyte common antigen. CD45 plays an important role in the function of the immune system by helping to regulate the activity of immune cells. It is also used as a marker to identify different types of immune cells in the laboratory. Antigens, CD45 refers to molecules that bind to CD45 on the surface of immune cells and trigger an immune response. These antigens can be found on viruses, bacteria, and other foreign substances, as well as on abnormal cells in the body.
Acridine Orange is a fluorescent dye that is commonly used in medical research and diagnostics. It is a cationic dye that binds to nucleic acids, specifically to double-stranded DNA and RNA, with high affinity. When Acridine Orange is added to a sample containing nucleic acids, it stains the nucleic acids bright orange, making them easily visible under a fluorescent microscope. Acridine Orange is often used as a stain in cytology to visualize cellular structures, such as chromosomes and nucleoli, in fixed and stained cells. It is also used in molecular biology to detect and quantify specific nucleic acid sequences, such as in PCR (polymerase chain reaction) assays. In addition, Acridine Orange has been used as an antiviral agent against certain viruses, such as herpes simplex virus and influenza virus. However, it is important to note that Acridine Orange is a mutagen and carcinogen, and its use should be carefully controlled and monitored to minimize potential risks to human health.
Technetium Tc 99m Exametazime is a radiopharmaceutical used in medical imaging to evaluate brain function. It is also known as HMPAO (hexamethylpropylene amine oxime) or Tc-99m HMPAO. The radiopharmaceutical is injected into a patient's bloodstream, and it is taken up by the brain cells. The radiopharmaceutical emits gamma rays that can be detected by a gamma camera to create images of the brain. This exam is commonly used to diagnose and monitor brain disorders such as Alzheimer's disease, brain tumors, and stroke.
Immune sera refers to a type of blood serum that contains antibodies produced by the immune system in response to an infection or vaccination. These antibodies are produced by B cells, which are a type of white blood cell that plays a key role in the immune response. Immune sera can be used to diagnose and treat certain infections, as well as to prevent future infections. For example, immune sera containing antibodies against a specific virus or bacteria can be used to diagnose a current infection or to prevent future infections in people who have been exposed to the virus or bacteria. Immune sera can also be used as a research tool to study the immune response to infections and to develop new vaccines and treatments. In some cases, immune sera may be used to treat patients with severe infections or allergies, although this is less common than using immune sera for diagnostic or preventive purposes.
Chemokine CXCL1, also known as Interleukin-8 (IL-8), is a type of protein that plays a crucial role in the immune system. It is a chemokine, which means that it is a type of signaling molecule that attracts immune cells to specific areas of the body in response to infection or injury. CXCL1 is produced by a variety of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. It is primarily involved in the recruitment of neutrophils to sites of inflammation, where they help to fight off infection and clear damaged tissue. In addition to its role in inflammation, CXCL1 has been implicated in a number of other biological processes, including cancer progression, angiogenesis (the formation of new blood vessels), and tissue repair. It is also a potential therapeutic target for the treatment of a variety of diseases, including cancer, autoimmune disorders, and inflammatory conditions.
An abscess is a localized collection of pus that forms in the body as a result of an infection. It is typically caused by bacteria or other microorganisms that enter the body through a wound or other opening, such as a tooth cavity or a surgical incision. The body's immune system responds to the infection by sending white blood cells to the area, which can lead to the formation of an abscess. Abscesses can occur in many different parts of the body, including the skin, muscles, joints, and organs. They can be painful and may cause redness, swelling, and warmth in the affected area. If left untreated, abscesses can become infected and spread to other parts of the body, potentially causing serious complications. Treatment for abscesses typically involves draining the pus and removing any infected tissue. This may be done through a surgical incision or by using a needle to drain the abscess. Antibiotics may also be prescribed to help fight the infection. In some cases, the abscess may recur if the underlying cause of the infection is not treated.
In the medical field, a focal infection refers to an infection that is localized or confined to a specific area of the body. This means that the infection is not widespread throughout the body and is contained within a particular organ, tissue, or region. Focal infections can be caused by a variety of microorganisms, including bacteria, viruses, fungi, and parasites. Examples of focal infections include pneumonia, which is an infection of the lungs, and cellulitis, which is an infection of the skin and underlying tissue. Focal infections can be treated with antibiotics, antiviral medications, antifungal medications, or antiparasitic medications, depending on the type of microorganism causing the infection. In some cases, surgery may be necessary to remove infected tissue or drain abscesses. It is important to diagnose and treat focal infections promptly to prevent complications and to prevent the infection from spreading to other parts of the body.
Receptors, Complement refers to a group of proteins that are part of the complement system, a complex network of proteins in the blood that helps to defend the body against infections. These receptors are located on the surface of immune cells, such as macrophages and neutrophils, and bind to specific molecules on the surface of pathogens, such as bacteria and viruses. This binding triggers a series of reactions that ultimately lead to the destruction of the pathogen. The complement receptors play a crucial role in the immune response and are important for the clearance of pathogens from the body.
Receptors, cell surface are proteins that are located on the surface of cells and are responsible for receiving signals from the environment. These signals can be chemical, electrical, or mechanical in nature and can trigger a variety of cellular responses. There are many different types of cell surface receptors, including ion channels, G-protein coupled receptors, and enzyme-linked receptors. These receptors play a critical role in many physiological processes, including sensation, communication, and regulation of cellular activity. In the medical field, understanding the function and regulation of cell surface receptors is important for developing new treatments for a wide range of diseases and conditions.
Annexin A1 is a protein that is expressed by a variety of cell types, including immune cells, epithelial cells, and endothelial cells. It is a member of the annexin family of proteins, which are characterized by their ability to bind to phospholipids and other molecules in the cell membrane. In the medical field, Annexin A1 has been studied for its potential role in a number of different processes, including inflammation, cell death, and cancer. It has been shown to have anti-inflammatory properties, and may play a role in regulating the immune response. It has also been implicated in the process of programmed cell death, or apoptosis, and may play a role in the development and progression of certain types of cancer. Annexin A1 has been the subject of a number of clinical trials, and is being investigated as a potential therapeutic target for a variety of diseases, including cancer, inflammatory disorders, and cardiovascular disease.
In the medical field, "latex" refers to a type of rubber that is commonly used to make medical equipment and supplies, such as gloves, catheters, and surgical instruments. Latex is a natural polymer that is derived from the sap of the rubber tree, and it is known for its strength, elasticity, and resistance to chemicals and heat. However, some people may be allergic to latex, which can cause a range of symptoms from mild itching to severe allergic reactions such as anaphylaxis. As a result, many medical facilities have started to use alternative materials, such as nitrile or vinyl, for medical equipment and supplies to accommodate individuals with latex allergies.
Reperfusion injury is a type of damage that occurs when blood flow is restored to an organ or tissue that has been deprived of oxygen for a prolonged period of time. This can happen during a heart attack, stroke, or other conditions that cause blood flow to be blocked to a particular area of the body. When blood flow is restored, it can cause an inflammatory response in the affected tissue, leading to the release of free radicals and other harmful substances that can damage cells and tissues. This can result in a range of symptoms, including swelling, pain, and organ dysfunction. Reperfusion injury can be particularly damaging to the heart and brain, as these organs are highly sensitive to oxygen deprivation and have a limited ability to repair themselves. Treatment for reperfusion injury may involve medications to reduce inflammation and prevent further damage, as well as supportive care to manage symptoms and promote healing.
Colchicine is a medication that is used to treat gout, a type of arthritis that is caused by the buildup of uric acid crystals in the joints. It works by inhibiting the production of certain chemicals in the body that are involved in the formation of uric acid crystals, which can help to reduce inflammation and pain in the joints. Colchicine is also sometimes used to treat familial Mediterranean fever, a genetic disorder that can cause recurrent episodes of fever and inflammation. It is usually taken by mouth, although it can also be given by injection. Common side effects of colchicine include nausea, vomiting, diarrhea, and abdominal pain.
CD53 is a protein that is expressed on the surface of certain immune cells, including T cells, B cells, and natural killer cells. It is a member of the immunoglobulin superfamily of proteins and plays a role in regulating immune cell activation and function. Antigens, CD53 refers to molecules that bind to the CD53 protein on the surface of immune cells. These antigens can be foreign substances, such as bacteria or viruses, or they can be self-antigens, which are proteins that are normally present in the body but can become abnormal and trigger an immune response. When an antigen binds to CD53, it can activate the immune cell and trigger an immune response, such as the production of antibodies or the release of cytokines.
Integrin alpha4beta1, also known as very late antigen-4 (VLA-4), is a cell surface protein that plays a crucial role in the adhesion and migration of immune cells, particularly leukocytes, to the endothelium of blood vessels. It is composed of two subunits, alpha4 and beta1, which are encoded by different genes. In the context of the immune system, integrin alpha4beta1 is involved in the homing of immune cells to specific tissues, such as the lymph nodes, spleen, and bone marrow. It also plays a role in the activation and differentiation of immune cells, as well as in the regulation of inflammation and immune responses. In addition to its role in the immune system, integrin alpha4beta1 has been implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases. For example, it has been shown to be involved in the metastasis of certain types of cancer cells, as well as in the pathogenesis of multiple sclerosis and rheumatoid arthritis. Overall, integrin alpha4beta1 is a key regulator of immune cell function and has important implications for the development and treatment of various diseases.
Interferon-gamma (IFN-γ) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by various immune cells, including T cells, natural killer cells, and macrophages, in response to viral or bacterial infections, as well as in response to certain types of cancer. IFN-γ has a wide range of effects on the immune system, including the activation of macrophages and other immune cells, the inhibition of viral replication, and the promotion of T cell differentiation and proliferation. It also plays a role in the regulation of the immune response, helping to prevent excessive inflammation and tissue damage. In the medical field, IFN-γ is used as a therapeutic agent in the treatment of certain types of cancer, such as Hodgkin's lymphoma and multiple myeloma. It is also being studied as a potential treatment for other conditions, such as autoimmune diseases and viral infections.
Leukostasis refers to the accumulation of white blood cells (leukocytes) in the microvasculature of the lungs, leading to impaired gas exchange and respiratory failure. This condition can occur in patients with certain medical conditions, such as sepsis, leukemia, or hyperviscosity syndrome, where there is an excessive number of white blood cells in the bloodstream. Leukostasis can also be caused by the use of certain medications, such as corticosteroids or chemotherapy drugs. Symptoms of leukostasis may include shortness of breath, coughing, chest pain, and fever. Treatment typically involves addressing the underlying cause of the leukostasis and providing supportive care to manage respiratory failure.
Cytomegalovirus (CMV) infections are a group of viral infections caused by the cytomegalovirus, a member of the herpesvirus family. CMV is a common virus that can infect people of all ages, but it is most commonly transmitted from mother to child during pregnancy or childbirth, or through breast milk. In healthy individuals, CMV infections are usually asymptomatic or cause mild flu-like symptoms. However, in people with weakened immune systems, such as those with HIV/AIDS, organ transplant recipients, or pregnant women with HIV, CMV infections can cause serious complications, including pneumonia, encephalitis, and retinitis. CMV infections can also be transmitted through blood transfusions, organ transplantation, and from mother to child during pregnancy or childbirth. Treatment for CMV infections typically involves antiviral medications to help control the virus and prevent complications.
Hydroxyquinolines are a class of organic compounds that contain a hydroxy group (-OH) attached to a quinoline ring. They are commonly used as antioxidants, anti-inflammatory agents, and antimalarial drugs. In the medical field, hydroxyquinolines are used to treat a variety of conditions, including: 1. Malaria: Hydroxychloroquine is a hydroxyquinoline that is used to treat and prevent malaria. 2. Rheumatoid arthritis: Hydroxychloroquine is also used to treat rheumatoid arthritis, a chronic inflammatory disorder that affects the joints. 3. Lupus: Hydroxychloroquine is used to treat systemic lupus erythematosus, a chronic autoimmune disorder that can affect multiple organs. 4. Psoriasis: Hydroxychloroquine is sometimes used to treat psoriasis, a chronic skin condition characterized by red, scaly patches on the skin. 5. Antimalarial prophylaxis: Hydroxychloroquine is also used as a prophylactic agent to prevent malaria in individuals who are at high risk of contracting the disease. Hydroxyquinolines can have side effects, including nausea, vomiting, diarrhea, and skin rashes. They can also cause liver damage, so patients taking hydroxyquinolines are monitored closely for liver function abnormalities.
Arachidonic acid is a polyunsaturated omega-6 fatty acid that is found in the cell membranes of all living organisms. It is an essential fatty acid, meaning that it cannot be synthesized by the body and must be obtained through the diet. In the medical field, arachidonic acid plays a significant role in various physiological processes, including inflammation, immune function, and blood clotting. It is also a precursor to the production of eicosanoids, a group of biologically active compounds that have diverse effects on the body, including vasodilation, vasoconstriction, and pain perception. Arachidonic acid is commonly found in foods such as fish, nuts, and seeds, and is also available as a dietary supplement. However, excessive consumption of arachidonic acid has been linked to an increased risk of certain health conditions, such as heart disease and cancer. Therefore, it is important to consume arachidonic acid in moderation as part of a balanced diet.
CD43 is a type of antigen found on the surface of certain cells in the immune system. It is a transmembrane glycoprotein that is expressed on most mature T cells, B cells, and natural killer cells. CD43 plays a role in cell adhesion and migration, and it is also involved in the regulation of immune responses. In the medical field, CD43 is often used as a marker to identify and study different types of immune cells, and it may also be used as a target for immunotherapy in certain diseases.
Defensins are a group of small, cationic peptides that are produced by various cells of the immune system, including neutrophils, macrophages, and epithelial cells. They are part of the innate immune system and play a crucial role in defending the body against infections caused by bacteria, viruses, fungi, and parasites. Defensins are characterized by their cysteine-rich, alpha-helical structure, which allows them to form stable complexes with negatively charged microbial membranes, leading to their disruption and killing. They also have anti-inflammatory and immunomodulatory properties, which help to regulate the immune response and prevent excessive tissue damage. Defensins are found in various body fluids, including saliva, tears, and sweat, as well as in the skin and mucous membranes. They are also present in the gut microbiome and have been shown to play a role in maintaining the balance of the gut microbiota. Defensins have been the subject of extensive research in the medical field due to their potential therapeutic applications in the treatment of various infectious and inflammatory diseases, including cystic fibrosis, inflammatory bowel disease, and cancer.
Lipoxygenase is an enzyme that catalyzes the oxidation of polyunsaturated fatty acids, particularly arachidonic acid, to produce a variety of bioactive compounds called eicosanoids. These compounds play important roles in various physiological processes, including inflammation, blood clotting, and immune responses. Lipoxygenase is found in many tissues throughout the body, including the lung, liver, and immune cells. In the medical field, lipoxygenase inhibitors are sometimes used to treat conditions such as asthma and inflammation.
Chemokine CCL5, also known as RANTES (regulated on activation, normal T cell expressed and secreted), is a small protein that plays a role in the immune system. It is a type of chemokine, which are signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL5 is produced by a variety of cells, including immune cells such as T cells, macrophages, and dendritic cells, as well as non-immune cells such as endothelial cells and fibroblasts. It acts on specific receptors on the surface of immune cells to attract them to the site of infection or injury. CCL5 has been implicated in a number of different diseases and conditions, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. It is also involved in the recruitment of immune cells to sites of inflammation, and has been shown to play a role in the development of autoimmune diseases such as rheumatoid arthritis. Overall, CCL5 is an important molecule in the immune system that helps to regulate the movement of immune cells and plays a role in the body's response to infection and injury.
Pleurisy is a medical condition characterized by inflammation of the pleura, which is the thin layer of tissue that covers the lungs and lines the inside of the chest cavity. This inflammation can cause the pleura to become thickened, sticky, and inflamed, leading to pain and difficulty breathing. There are two types of pleurisy: viral and bacterial. Viral pleurisy is usually caused by a respiratory virus, such as the flu or COVID-19, and is usually self-limiting. Bacterial pleurisy, on the other hand, is caused by bacteria and requires antibiotics to treat. Symptoms of pleurisy may include chest pain that worsens with deep breathing or coughing, difficulty breathing, fever, and a dry cough. Treatment for pleurisy typically involves pain management, antibiotics if the cause is bacterial, and rest. In severe cases, hospitalization may be necessary.
Integrins are a family of transmembrane proteins that play a crucial role in cell adhesion and signaling. They are composed of two subunits, alpha and beta, which form a heterodimer that spans the cell membrane. Integrins bind to various extracellular matrix proteins, such as fibronectin, laminin, and collagen, and transmit signals across the cell membrane to the cytoplasm. This process is essential for cell migration, tissue development, and immune function. In the medical field, integrins are important targets for the development of drugs to treat various diseases, including cancer, autoimmune disorders, and cardiovascular diseases.
Receptors, Leukotriene B4 (LTB4) are a type of protein receptor found on the surface of certain cells in the immune system, such as neutrophils and macrophages. These receptors are activated by the binding of the signaling molecule leukotriene B4 (LTB4), which is produced by immune cells in response to inflammation or infection. When LTB4 binds to its receptor, it triggers a cascade of intracellular signaling events that can lead to a variety of cellular responses, including the activation and recruitment of immune cells to the site of inflammation, the production of pro-inflammatory cytokines and chemokines, and the promotion of tissue damage. In the medical field, the study of LTB4 receptors and their role in inflammation and immune responses is important for understanding the pathophysiology of a variety of diseases, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. In addition, drugs that target LTB4 receptors are being developed as potential treatments for these conditions.
Leukocyte esterase
Leukocyte extravasation
Leucocyte (disambiguation)
Passenger leukocyte
Leucocyte (album)
Leukocyte apheresis
Leukocyte adhesion deficiency
Dog leukocyte antigen
Leukocyte-promoting factor
Human leukocyte antigen
Leukocyte adhesion deficiency-1
Leukocyte adhesion molecule deficiency
Leukocyte immunoglobulin-like receptors
Leukocyte receptor tyrosine kinase
Journal of Leukocyte Biology
Leukocyte immunoglobulin-like receptor pseudogene 2
List of human leukocyte antigen alleles associated with cutaneous conditions
Plasmacytoid dendritic cell
TAAR1
List of Guilty Crown characters
Coelomocyte
Thomas P. Stossel
Toxic vacuolation
Alberto Mantovani
List of Guilty Crown episodes
Cortisol
Uremic pericarditis
List of immune cells
Gábor Palotai
Apheresis
Leukocyte adhesion deficiency type 1: MedlinePlus Genetics
Leukocyte Adhesion Deficiency: Background, Pathophysiology, Epidemiology
NHANES 2009-2009: Human Leukocyte Antigen B-27 Data Documentation, Codebook, and Frequencies
Immunity Cells in Blood (Innate Immunity Signal Transduction in Human Leukocytes)
Leukocyte-Autoantibodies | Acta Haematologica | Karger Publishers
Figure 3 - Human Diversity of Killer Cell Immunoglobulin-Like Receptors and Human Leukocyte Antigen Class I Alleles and Ebola...
Transcript origin analysis identifies antigen-presenting cells as primary targets of socially regulated gene expression in...
EMF-Portal | leukocytes
LOINC 10579-1 Leukocytes [#/volume] in Semen
Isolation of Infiltrating Leukocytes from Mouse Skin Using Enzymatic Digest and Gradient Separation | Protocol
Evaluation of Yumizen H2500/1500 and Sysmex XN1000 leukocyte diff count for leukemias detection
Frontiers | Optimization of Biomimetic, Leukocyte-Mimicking Nanovesicles for Drug Delivery Against Colorectal Cancer Using a...
Leukocyte Adhesion Deficiency - Immune Disorders - MSD Manual Consumer Version
Leukocyte Telomere Length Predicts Cancer Risk in Barrett's Esophagus | Cancer Epidemiology, Biomarkers & Prevention | American...
Exposure to arsenic at different life-stages and DNA methylation meta-analysis in buccal cells and leukocytes | Academic Commons
ZFIN Anatomy Ontology: leukocyte
Increased risk of human leukocyte antigen-G gene variants in Behçet`s disease
Within lymph nodes non-hematopoietic stromal cells interact and organize with leukocytes | immune-source.com
Leukocyte Adhesion Deficiency Differential Diagnoses
Leukocyte Adhesion Deficiency: Background, Pathophysiology, Epidemiology
Leukocytes | Pharmacognosy Journal
platelets with leukocytes | Interesting Medical Facts
Prediction of leukocyte counts during paediatric acute lymphoblastic leukaemia maintenance therapy - Trepo
Thrombocytopenia Associated with Elemental Mercury Poisoning in Two Siblings - Connecticut, July 2022 | MMWR
Department of Pathology - Nick Lukacs, PhD Named President-Elect of Society for Leukocyte Biology
Improved Leukocyte Detection Algorithm of YOLOv5
Characterization of 108 Genomic DNA Reference Materials for 11 Human Leukocyte Antigen Loci
Elsevier: Côté: Clinical Veterinary Advisor, 3rd Edition · Leukocytes (Leukocytosis/Leukopenia)
Low grade inflammation and coronary heart disease: prospective study and updated meta-analyses | The BMJ
Adhesion49
- Leukocyte adhesion deficiency type 1 is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. (medlineplus.gov)
- Starting from birth, people with leukocyte adhesion deficiency type 1 develop serious bacterial and fungal infections. (medlineplus.gov)
- One of the first signs of leukocyte adhesion deficiency type 1 is a delay in the detachment of the umbilical cord stump after birth. (medlineplus.gov)
- but, in infants with leukocyte adhesion deficiency type 1, this separation usually occurs at three weeks or later. (medlineplus.gov)
- In leukocyte adhesion deficiency type 1, bacterial and fungal infections most commonly occur on the skin and mucous membranes such as the moist lining of the nose and mouth. (medlineplus.gov)
- A hallmark of leukocyte adhesion deficiency type 1 is the lack of pus formation at the sites of infection. (medlineplus.gov)
- Life expectancy in individuals with leukocyte adhesion deficiency type 1 is often severely shortened. (medlineplus.gov)
- Leukocyte adhesion deficiency type 1 is estimated to occur in 1 per million people worldwide. (medlineplus.gov)
- Mutations in the ITGB2 gene cause leukocyte adhesion deficiency type 1. (medlineplus.gov)
- This binding leads to linkage (adhesion) of the leukocyte to the blood vessel wall. (medlineplus.gov)
- ITGB2 gene mutations that cause leukocyte adhesion deficiency type 1 lead to the production of a β2 subunit that cannot bind with other subunits to form β2 integrins. (medlineplus.gov)
- Cox DP, Weathers DR. Leukocyte adhesion deficiency type 1: an important consideration in the clinical differential diagnosis of prepubertal periodontitis. (medlineplus.gov)
- Leukocyte adhesion deficiency (LAD) is a rare primary immunodeficiency. (medscape.com)
- Thus the infections in patients with leukocyte adhesion deficiency act similarly as those observed in patients with neutropenia. (medscape.com)
- Labial ulceration from which Escherichia coli was cultured in an 8-month-old girl with leukocyte adhesion deficiency type 1 (LAD I). Note the thin bluish scar at the superior aspect of the labia from an earlier cellulitis. (medscape.com)
- This 3-year-old girl had leukocyte adhesion deficiency type I (LAD I) with complete absence of CD18 expression. (medscape.com)
- This 10-month-old patient with severe leukocyte adhesion deficiency type I (LAD I) developed a cervical adenitis caused by Klebsiella pneumoniae. (medscape.com)
- Leukocyte adhesion deficiency type I (LAD I) is a failure to express CD18, which composes the common ß 2 subunit of LFA1 family (ß2 integrins). (medscape.com)
- In milder forms of leukocyte adhesion deficiency I (1-30% expression of CD8), patients may survive to adulthood. (medscape.com)
- Patients with leukocyte adhesion deficiency II manifest the Bombay phenotype (ie, negative for O and H blood group antigens with potential production of anti-H antibody). (medscape.com)
- However, IgM and IgG serum levels are within the reference range in patients with leukocyte adhesion deficiency II. (medscape.com)
- Leukocyte adhesion deficiency II may be classified as one of the congenital disorders of glycosylation (CDG), a rapidly expanding group of metabolic syndromes with a wide symptomatology and severity. (medscape.com)
- Currently, 18 subtypes have been reported: 12 are type I (dysfunctional lipid-linked oligosaccharide precursor synthesis), and 6 are type II (dysfunctional trimming/processing of the protein-bound oligosaccharide), including leukocyte adhesion deficiency II (CDG-IIc). (medscape.com)
- Variants of leukocyte adhesion deficiency have also been reported, including fully expressed but nonfunctional CD18 and an E selectin that is expressed but rapidly cleaved from the cell surface (only present in soluble form). (medscape.com)
- Another reported type of leukocyte adhesion deficiency involves dysfunction in platelet aggregation in addition to a defect in leukocyte adhesion. (medscape.com)
- Thus, patients with this type of leukocyte adhesion deficiency manifest both severe bacterial infections and bleeding disorder. (medscape.com)
- This leukocyte adhesion deficiency variant is associated with defective expression of the Rap-1 activator CalDAG-GEFI. (medscape.com)
- Leukocyte adhesion deficiency type 1 (LAD-1) is a rare disease resulting from mutations in the gene encoding for the common β-chain of the β2-integrin family (CD18). (jci.org)
- Leukocyte adhesion deficiency is an immunodeficiency disorder in which white blood cells (leukocytes) do not function normally, causing frequent soft-tissue infections. (msdmanuals.com)
- Symptoms of leukocyte adhesion deficiency usually begin during infancy and include frequent infections in soft tissues, such as the gums, skin, and muscles. (msdmanuals.com)
- Symptoms of leukocyte adhesion deficiency usually begin during infancy. (msdmanuals.com)
- In children with one form of leukocyte adhesion deficiency, intellectual and physical development is often slow. (msdmanuals.com)
- Also, special blood tests, including analysis of proteins on the surface of white blood cells (called flow cytometry), are used to diagnose leukocyte adhesion deficiency. (msdmanuals.com)
- Treatment of leukocyte adhesion deficiency includes antibiotics, often given continuously, to prevent infections. (msdmanuals.com)
- These leukocyte adhesion deficiencies (LADs) are unlikely to be confused with hyperimmunoglobulin E syndrome or chronic granulomatous disease because the clinical features of infection resemble those manifested by patients with severe neutropenia despite marked neutrophilia. (medscape.com)
- A defect in a guanosine triphosphate (GTP)-binding protein, Rac2, which is integral to actin-associated neutrophil responses and to the generation of superoxide by nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, leads to a clinical syndrome resembling Leukocyte adhesion deficiency with prolonged cord attachment, perirectal cellulitis, and omphalitis associated with marked leukocytosis and poor wound healing. (medscape.com)
- The absence of leukocytosis distinguishes healthy infants from those with leukocyte adhesion deficiency. (medscape.com)
- Hanna S, Etzioni A. Leukocyte adhesion deficiencies. (medscape.com)
- Cagdas D, Yilmaz M, Kandemir N, Tezcan I, Etzioni A, Sanal O. A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc. (medscape.com)
- Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter. (medscape.com)
- LAD-III, a leukocyte adhesion deficiency syndrome associated with defective Rap1 activation and impaired stabilization of integrin bonds. (medscape.com)
- Two mutations in the KINDLIN3 gene of a new leukocyte adhesion deficiency III patient reveal distinct effects on leukocyte function in vitro. (medscape.com)
- Preimplantation genetic diagnosis of leukocyte adhesion deficiency type I. Fertil Steril . (medscape.com)
- Hematopoetic Stem Cell Transplantation in Neutrophil Disorders: Severe Congenital Neutropenia, Leukocyte Adhesion Deficiency and Chronic Granulomatous Disease. (medscape.com)
- Leukocyte Adhesion Deficiency Type III: Clinical Features and Treatment With Stem Cell Transplantation. (medscape.com)
- Defective neutrophil recruitment in leukocyte adhesion deficiency type I disease causes local IL-17-driven inflammatory bone loss. (medscape.com)
- A novel genetic leukocyte adhesion deficiency in subsecond triggering of integrin avidity by endothelial chemokines results in impaired leukocyte arrest on vascular endothelium under shear flow. (medscape.com)
- Gene therapy for leukocyte adhesion deficiency. (medscape.com)
- Nonmyeloablative hematopoietic stem cell transplantation corrects the disease phenotype in the canine model of leukocyte adhesion deficiency. (medscape.com)
Deficiency1
- The severe and moderate phenotypes of heritable Mac-1, LFA-1 deficiency: their quantitative definition and relation to leukocyte dysfunction and clinical features. (medscape.com)
Vitro2
- While there is mounting in vitro evidence to suggest that ANCAs are capable of enhancing leukocyte-endothelial interactions, no in vivo evidence for this has been provided. (tcd.ie)
- To assess the role of shark cartilage as an immune modulator, acid, salt-soluble, and phosphate-buffered saline extracts were prepared from three different commercial sources (SL, TL, FDC) of cartilage and used to stimulate human leukocytes in vitro. (fiu.edu)
Loci1
- In 2014, Genome-Wide Association Study (GWAS) was performed with 2,398 individuals with laryngeal squamous cell carcinoma cases and 2,804 cancer-free controls from Chinese populations, and identified a novel susceptibility loci in complex human leukocyte antigen (HLA), which plays crucial role in immune response. (who.int)
Mediate3
- These 2 members mediate leukocyte adhesions to endothelial cells but they also serve as receptors for iC3b (inactivated C3b). (medscape.com)
- DNA sequence variation within human leukocyte antigen (HLA) genes mediate susceptibility to a wide range of human diseases. (nih.gov)
- Leukocytes or white blood cells (WBCs) are immune cells that fight infection, neoplasms and other inflammatory conditions, and mediate allergic responses. (loinc.org)
Peripheral4
- The results of the leukocyte differential count showed the same cell types found in the morphology of the peripheral blood smear and bone marrow aspiration. (horiba.com)
- There was no difference in the leukocyte differential count parameters between both hematology analyzers and had a significant positive correlation with the morphology of the peripheral blood smear and bone marrow aspiration. (horiba.com)
- NOD/LtSz-Rag1nullPfpnull mice: a new model system with increased levels of human peripheral leukocyte and hematopoietic stem-cell engraftment. (umassmed.edu)
- Although psychological stress is known to modulate immune function, mechanistic pathways linking stress networks in the brain to peripheral leukocytes remain poorly understood2. (bvsalud.org)
Endothelium1
- Specifically, the use of leukocyte-derived membrane proteins to functionalize nanovesicles (leukosomes) can enable their long circulation and target the inflamed endothelium present in many inflammatory pathologies and tumors, making them a promising and versatile drug delivery system. (frontiersin.org)
Endothelial2
- This disease is a defect in fucose metabolism (lack of fucosylation of the carbohydrate selectin ligands) that results in failure to express the ligand for E and P selectin, sialyl Lewis-X (CD15s) expressed on leukocytes and endothelial cells. (medscape.com)
- This study provides the first direct in vivo evidence for the ability of ANCAs to enhance leukocyte-endothelial interactions and cause microvascular hemorrhage, thereby providing a mechanism by which ANCAs could exert pathogenic effects in systemic vasculitis. (tcd.ie)
Infections1
- [ 1 , 2 ] The clinical picture is characterized by marked leukocytosis and localized bacterial infections that are difficult to detect until they have progressed to an extensive level secondary to lack of leukocyte recruitment at the site of infection. (medscape.com)
Cells4
- The Innate Immunity Signal Transduction in Human Leukocytes is a research study to determine the response of immune cells from the bloodstream. (nih.gov)
- Duplicate leukocyte cultures were set up, each containing 50 $\mu$l of endotoxin-free extract, 200 $\mu$l of cell suspension (2.4-2.5 $\times$ 10$\sp5$ cells) and 100 $\mu$l of medium and incubated at 37$\sp\circ$C. Cultures stimulated with LPS (5 $\mu$g/ml) or medium served as the positive and negative controls, respectively. (fiu.edu)
- To investigate whether leukocyte-expressed PSGL-1 is mediating L-selectin-dependent rolling, we reconstituted lethally irradiated wild-type mice with PSGL-1 −/− bone marrow cells. (rupress.org)
- Similar survival rates were found for leukocytes (88%) and epithelial cells (10%) after rinsing with Listerine mouthwash. (cdc.gov)
Human5
- An association between Human Leukocyte Histocompatibility Antigen B-27 (HLA-B27) and major arthritis syndromes such as Ankylosing Spondylitis and Reactive Arthritis is well documented (Khan et al. (cdc.gov)
- HLA, human leukocyte antigen. (cdc.gov)
- Polysialic acid, a glycan with highly restricted expression, is found on human and murine leukocytes and modulates immune responses. (ca.gov)
- In this study a novel rat model of ANCA-associated experimental autoimmune vasculitis (EAV), induced by immunization with human myeloperoxidase (MPO), was used to analyze directly the potential effect of ANCAs on leukocyte-venular wall interactions in vivo as observed by intravital microscopy. (tcd.ie)
- Moreover, leukocytes appear to be a more reliable source of human tissue for assessing DNA damage and possibly other biochemical changes. (cdc.gov)
Counts1
- Both elevated and low leukocyte counts can be markers of infection and malignancy, and low leukocyte counts are associated with a variety of primary and secondary immunodeficiencies, depending on the WBC type(s) that are out of range. (loinc.org)
Diagnosis1
- In leukemia, hematological parameters especially in the case of leukocyte differential count helps early diagnosis of leukemia. (horiba.com)
Distinct1
- Here we show that distinct brain regions shape leukocyte distribution and function throughout the body during acute stress in mice . (bvsalud.org)
Interactions1
- Antineutrophil cytoplasm antibodies directed against myeloperoxidase augment leukocyte-microvascular interactions in vivo. (tcd.ie)
Diseases1
- Purpose: Leukocyte telomere length has gained attention as a marker of oxidative damage and age-related diseases, including cancer. (aacrjournals.org)
Antibodies1
- Leukocyte rolling in postcapillary venules of inflamed tissues is reduced in L-selectin-deficient mice and mice treated with L-selectin blocking antibodies, but the glycoprotein ligand for L-selectin in inflamed venules is unknown. (rupress.org)
Immune responses1
- We also detected changes in energy utilization and immune responses in leukocytes from older cows. (biomedcentral.com)
MeSH1
- Leukocyte Transfusion" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (umassmed.edu)
Evaluation1
- Evaluation of children with possible appendicitis using technetium 99m leukocyte scan. (umassmed.edu)
Blood2
- Signaling through the β2 integrins triggers the transport of the attached leukocyte across the blood vessel wall to the site of infection or injury. (medlineplus.gov)
- Leukocytes that lack these integrins cannot attach to the blood vessel wall or cross the vessel wall to contribute to the immune response. (medlineplus.gov)
Separation2
People2
- This graph shows the total number of publications written about "Leukocyte Transfusion" by people in this website by year, and whether "Leukocyte Transfusion" was a major or minor topic of these publications. (umassmed.edu)
- Below are the most recent publications written about "Leukocyte Transfusion" by people in Profiles. (umassmed.edu)
Patients1
- We hypothesize that leukocyte telomere length might be able to predict future risk of cancer and examined this in a cohort of patients with Barrett's esophagus, who are at increased risk of esophageal adenocarcinoma and thus were enrolled in a long-term cancer surveillance program. (aacrjournals.org)
Method1
- Though this method can provide insight into skin-infiltrating leukocyte biology, it can also be applied to the investigation of other resident cell populations. (jove.com)
Early1
- This study analysed the transcriptome derived from RNA-seq data of leukocytes obtained from Holstein cows in early lactation with respect to lactation number. (biomedcentral.com)