HTLV-I (Human T-lymphotropic virus type 1) infection is a retroviral infection that primarily targets CD4+ T-cells, potentially leading to the development of adult T-cell leukemia/lymphoma and tropical spastic paraparesis/myelopathy (TSP/HAM), as well as other inflammatory diseases.
A strain of PRIMATE T-LYMPHOTROPIC VIRUS 1 isolated from mature T4 cells in patients with T-lymphoproliferation malignancies. It causes adult T-cell leukemia (LEUKEMIA-LYMPHOMA, T-CELL, ACUTE, HTLV-I-ASSOCIATED), T-cell lymphoma (LYMPHOMA, T-CELL), and is involved in mycosis fungoides, SEZARY SYNDROME and tropical spastic paraparesis (PARAPARESIS, TROPICAL SPASTIC).
A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239)
HTLV-II (Human T-lymphotropic virus type II) infections are chronic viral infections primarily involving the CD4+ T lymphocytes, which can lead to adult T-cell leukemia/lymphoma, myelopathy/tropical spastic paraparesis, and other inflammatory diseases, but with a lower prevalence and geographical distribution compared to HTLV-I.
Antibodies reactive with the HTLV-I ANTIGENS.
An island in the Greater Antilles in the West Indies. Its capital is Kingston. It was discovered in 1494 by Columbus and was a Spanish colony 1509-1655 until captured by the English. Its flourishing slave trade was abolished in the 19th century. It was a British colony 1655-1958 and a territory of the West Indies Federation 1958-62. It achieved full independence in 1962. The name is from the Arawak Xaymaca, rich in springs or land of springs. (From Webster's New Geographical Dictionary, 1988, p564 & Room, Brewer's Dictionary of Names, 1992, p267)
A strain of PRIMATE T-LYMPHOTROPIC VIRUS 2 that can transform normal T-lymphocytes and can replicate in both T- and B-cell lines. The virus is related to but distinct from HTLV-1.
Transcriptional trans-acting proteins of the promoter elements found in the long terminal repeats (LTR) of HUMAN T-LYMPHOTROPIC VIRUS 1 and HUMAN T-LYMPHOTROPIC VIRUS 2. The tax (trans-activator x; x is undefined) proteins act by binding to enhancer elements in the LTR.
A genus in the family RETROVIRIDAE consisting of exogenous horizontally-transmitted viruses found in a few groups of mammals. Infections caused by these viruses include human B- or adult T-cell leukemia/lymphoma (LEUKEMIA-LYMPHOMA, T-CELL, ACUTE, HTLV-I-ASSOCIATED), and bovine leukemia (ENZOOTIC BOVINE LEUKOSIS). The type species is LEUKEMIA VIRUS, BOVINE.
Duplex DNA sequences in eukaryotic chromosomes, corresponding to the genome of a virus, that are transmitted from one cell generation to the next without causing lysis of the host. Proviruses are often associated with neoplastic cell transformation and are key features of retrovirus biology.
Infections caused by the HTLV or BLV deltaretroviruses. They include human T-cell leukemia-lymphoma (LEUKEMIA-LYMPHOMA, T-CELL, ACUTE, HTLV-I-ASSOCIATED).
The condition of harboring an infective organism without manifesting symptoms of infection. The organism must be readily transmissible to another susceptible host.
DNA sequences that form the coding region for at least three proteins which regulate the expression of HUMAN T-LYMPHOTROPIC VIRUS 1 and HUMAN T-LYMPHOTROPIC VIRUS 2. The proteins are p21(x), p27(rex), and p40(tax). The tax (trans-activator x) and rex (regulator x) genes are part of pX but are in overlapping reading frames. X was the original designation for the sequences or region (at that time of unknown function) in the long open reading frame (lor) which is now called pX.
Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa.
The quantity of measurable virus in a body fluid. Change in viral load, measured in plasma, is sometimes used as a SURROGATE MARKER in disease progression.
Mature LYMPHOCYTES and MONOCYTES transported by the blood to the body's extravascular space. They are morphologically distinguishable from mature granulocytic leukocytes by their large, non-lobed nuclei and lack of coarse, heavily stained cytoplasmic granules.
Immunoglobulins produced in response to VIRAL ANTIGENS.
Lymphocytes responsible for cell-mediated immunity. Two types have been identified - cytotoxic (T-LYMPHOCYTES, CYTOTOXIC) and helper T-lymphocytes (T-LYMPHOCYTES, HELPER-INDUCER). They are formed when lymphocytes circulate through the THYMUS GLAND and differentiate to thymocytes. When exposed to an antigen, they divide rapidly and produce large numbers of new T cells sensitized to that antigen.
Deoxyribonucleic acid that makes up the genetic material of viruses.
## I'm sorry for any confusion, but "Japan" is not a medical term or concept. It is a country located in Asia, known as Nihon-koku or Nippon-koku in Japanese, and is renowned for its unique culture, advanced technology, and rich history. If you have any questions related to medical topics, I would be happy to help answer them!
Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea.
An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993.
Antibodies reactive with various types of human T-cell leukemia/lymphoma antigens or bovine leukemia virus antigens.
Established cell cultures that have the potential to propagate indefinitely.
A strain of PRIMATE T-LYMPHOTROPIC VIRUS 2, closely related to the human HTLV-1 virus. The clinical, hematological, and histopathological characteristics of the disease in STLV-infected monkeys are very similar to those of human adult T-cell leukemia. Subgroups include the African green monkey subtype (STLV-I-AGM), for which the nucleotide sequence is 95% homologous with that of HUMAN T-LYMPHOTROPIC VIRUS 1, and the Asian rhesus macaque subtype (STLV-I-MM), for which the nucleotide sequence is 90% homologous with that of HUMAN T-LYMPHOTROPIC VIRUS 1.
Antibodies reactive with the HTLV-II ANTIGENS.
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Antigens associated with the DELTARETROVIRUS; HTLV-I ANTIGENS and HTLV-II ANTIGENS belong to this group.
A species of DELTARETROVIRUS that includes the strains SIMIAN T-LYMPHOTROPIC VIRUS 3 and HUMAN T-LYMPHOTROPIC VIRUS 3.
Retroviral proteins that have the ability to transform cells. They can induce sarcomas, leukemias, lymphomas, and mammary carcinomas. Not all retroviral proteins are oncogenic.
Antigens associated with HUMAN T-LYMPHOTROPIC VIRUS 1.
Morphologic alteration of small B LYMPHOCYTES or T LYMPHOCYTES in culture into large blast-like cells able to synthesize DNA and RNA and to divide mitotically. It is induced by INTERLEUKINS; MITOGENS such as PHYTOHEMAGGLUTININS, and by specific ANTIGENS. It may also occur in vivo as in GRAFT REJECTION.
Antigens associated with HUMAN T-LYMPHOTROPIC VIRUS 2.
A French overseas department on the northeast coast of South America. Its capital is Cayenne. It was first settled by the French in 1604. Early development was hindered because of the presence of a penal colony. The name of the country and the capital are variants of Guyana, possibly from the native Indian Guarani guai (born) + ana (kin), implying a united and interrelated race of people. (From Webster's New Geographical Dictionary, 1988, p418 & Room, Brewer's Dictionary of Names, 1992, p195)
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A classification of T-lymphocytes, especially into helper/inducer, suppressor/effector, and cytotoxic subsets, based on structurally or functionally different populations of cells.
Retroviral proteins, often glycosylated, coded by the envelope (env) gene. They are usually synthesized as protein precursors (POLYPROTEINS) and later cleaved into the final viral envelope glycoproteins by a viral protease.
Viruses whose genetic material is RNA.
A genus of the subfamily CERCOPITHECINAE inhabiting the African forests. They are also known as mangabeys.
The process of intracellular viral multiplication, consisting of the synthesis of PROTEINS; NUCLEIC ACIDS; and sometimes LIPIDS, and their assembly into a new infectious particle.
Post-transcriptional regulatory proteins required for the accumulation of mRNAs that encode the gag and env gene products in HUMAN T-LYMPHOTROPIC VIRUS 1 and HUMAN T-LYMPHOTROPIC VIRUS 2. The rex (regulator x; x is undefined) products act by binding to elements in the LONG TERMINAL REPEAT.
The type species of ORTHOPOXVIRUS, related to COWPOX VIRUS, but whose true origin is unknown. It has been used as a live vaccine against SMALLPOX. It is also used as a vector for inserting foreign DNA into animals. Rabbitpox virus is a subspecies of VACCINIA VIRUS.
A CELL LINE derived from human T-CELL LEUKEMIA and used to determine the mechanism of differential susceptibility to anti-cancer drugs and radiation.
A critical subpopulation of T-lymphocytes involved in the induction of most immunological functions. The HIV virus has selective tropism for the T4 cell which expresses the CD4 phenotypic marker, a receptor for HIV. In fact, the key element in the profound immunosuppression seen in HIV infection is the depletion of this subset of T-lymphocytes.
A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood.
Specific molecular components of the cell capable of recognizing and interacting with a virus, and which, after binding it, are capable of generating some signal that initiates the chain of events leading to the biological response.
The collective name for the islands of the Pacific Ocean northeast of Australia, including NEW CALEDONIA; VANUATU; New Hebrides, Solomon Islands, Admiralty Islands, Bismarck Archipelago, FIJI, etc. Melanesia (from the Greek melas, black + nesos, island) is so called from the black color of the natives who are generally considered to be descended originally from the Negroid Papuans and the Polynesians or Malays. (From Webster's New Geographical Dictionary, 1988, p748 & Room, Brewer's Dictionary of Names, 1992, p344)
The functional hereditary units of VIRUSES.
'Blood donors' are individuals who voluntarily and safely donate a specific amount of their own blood, which can be further separated into components, to be used for transfusion purposes or for manufacturing medical products, without receiving remuneration that is intended to reward them financially.
Individual members of Central American ethnic groups with ancient historic ancestral origins in Asia. Mexican Indians are not included.
Proteins from the family Retroviridae. The most frequently encountered member of this family is the Rous sarcoma virus protein.
A strain of PRIMATE T-LYMPHOTROPIC VIRUS 3 that is genetically similar to STLV-3.
An inheritable change in cells manifested by changes in cell division and growth and alterations in cell surface properties. It is induced by infection with a transforming virus.
Process of growing viruses in live animals, plants, or cultured cells.
The relationships of groups of organisms as reflected by their genetic makeup.
Virus diseases caused by the RETROVIRIDAE.
Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2.
Substances elaborated by viruses that have antigenic activity.
A species of parasitic nematode widely distributed in tropical and subtropical countries. The females and their larvae inhabit the mucosa of the intestinal tract, where they cause ulceration and diarrhea.
Any of the processes by which cytoplasmic factors influence the differential control of gene action in viruses.
The expelling of virus particles from the body. Important routes include the respiratory tract, genital tract, and intestinal tract. Virus shedding is an important means of vertical transmission (INFECTIOUS DISEASE TRANSMISSION, VERTICAL).
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Ribonucleic acid that makes up the genetic material of viruses.
Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES).
Proteins found in any species of virus.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
A general term for diseases produced by viruses.
Nucleotide sequences repeated on both the 5' and 3' ends of a sequence under consideration. For example, the hallmarks of a transposon are that it is flanked by inverted repeats on each end and the inverted repeats are flanked by direct repeats. The Delta element of Ty retrotransposons and LTRs (long terminal repeats) are examples of this concept.
A species of POLYOMAVIRUS originally isolated from Rhesus monkey kidney tissue. It produces malignancy in human and newborn hamster kidney cell cultures.
Individual members of South American ethnic groups with historic ancestral origins in Asia.
Sensitive assay using radiolabeled ANTIGENS to detect specific ANTIBODIES in SERUM. The antigens are allowed to react with the serum and then precipitated using a special reagent such as PROTEIN A sepharose beads. The bound radiolabeled immunoprecipitate is then commonly analyzed by gel electrophoresis.
The assembly of VIRAL STRUCTURAL PROTEINS and nucleic acid (VIRAL DNA or VIRAL RNA) to form a VIRUS PARTICLE.
Viruses parasitic on plants higher than bacteria.
Viruses whose nucleic acid is DNA.
Visible morphologic changes in cells infected with viruses. It includes shutdown of cellular RNA and protein synthesis, cell fusion, release of lysosomal enzymes, changes in cell membrane permeability, diffuse changes in intracellular structures, presence of viral inclusion bodies, and chromosomal aberrations. It excludes malignant transformation, which is CELL TRANSFORMATION, VIRAL. Viral cytopathogenic effects provide a valuable method for identifying and classifying the infecting viruses.
Viruses which lack a complete genome so that they cannot completely replicate or cannot form a protein coat. Some are host-dependent defectives, meaning they can replicate only in cell systems which provide the particular genetic function which they lack. Others, called SATELLITE VIRUSES, are able to replicate only when their genetic defect is complemented by a helper virus.
A broad category of viral proteins that play indirect roles in the biological processes and activities of viruses. Included here are proteins that either regulate the expression of viral genes or are involved in modifying host cell functions. Many of the proteins in this category serve multiple functions.
DNA sequences that form the coding region for the viral envelope (env) proteins in retroviruses. The env genes contain a cis-acting RNA target sequence for the rev protein (= GENE PRODUCTS, REV), termed the rev-responsive element (RRE).
I'm sorry for any confusion, but "Peru" is not a medical term or concept, it is a country located in South America, known officially as the Republic of Peru. If you have any questions about medical topics that I can help clarify, please let me know!
Sequences of DNA or RNA that occur in multiple copies. There are several types: INTERSPERSED REPETITIVE SEQUENCES are copies of transposable elements (DNA TRANSPOSABLE ELEMENTS or RETROELEMENTS) dispersed throughout the genome. TERMINAL REPEAT SEQUENCES flank both ends of another sequence, for example, the long terminal repeats (LTRs) on RETROVIRUSES. Variations may be direct repeats, those occurring in the same direction, or inverted repeats, those opposite to each other in direction. TANDEM REPEAT SEQUENCES are copies which lie adjacent to each other, direct or inverted (INVERTED REPEAT SEQUENCES).
The type species of ALPHAVIRUS normally transmitted to birds by CULEX mosquitoes in Egypt, South Africa, India, Malaya, the Philippines, and Australia. It may be associated with fever in humans. Serotypes (differing by less than 17% in nucleotide sequence) include Babanki, Kyzylagach, and Ockelbo viruses.
The type species of MORBILLIVIRUS and the cause of the highly infectious human disease MEASLES, which affects mostly children.
Proteins coded by the retroviral gag gene. The products are usually synthesized as protein precursors or POLYPROTEINS, which are then cleaved by viral proteases to yield the final products. Many of the final products are associated with the nucleoprotein core of the virion. gag is short for group-specific antigen.
A subtype of INFLUENZA A VIRUS with the surface proteins hemagglutinin 1 and neuraminidase 1. The H1N1 subtype was responsible for the Spanish flu pandemic of 1918.
EPIDEMIOLOGIC STUDIES based on the detection through serological testing of characteristic change in the serum level of specific ANTIBODIES. Latent subclinical infections and carrier states can thus be detected in addition to clinically overt cases.
Eukaryotic cell line obtained in a quiescent or stationary phase which undergoes conversion to a state of unregulated growth in culture, resembling an in vitro tumor. It occurs spontaneously or through interaction with viruses, oncogenes, radiation, or drugs/chemicals.
Skin diseases caused by viruses.
Proteins encoded by the ENV GENE of the HUMAN IMMUNODEFICIENCY VIRUS.
The type species of LYSSAVIRUS causing rabies in humans and other animals. Transmission is mostly by animal bites through saliva. The virus is neurotropic multiplying in neurons and myotubes of vertebrates.
DNA sequences that form the coding region for retroviral enzymes including reverse transcriptase, protease, and endonuclease/integrase. "pol" is short for polymerase, the enzyme class of reverse transcriptase.
A subtype of INFLUENZA A VIRUS comprised of the surface proteins hemagglutinin 5 and neuraminidase 1. The H5N1 subtype, frequently referred to as the bird flu virus, is endemic in wild birds and very contagious among both domestic (POULTRY) and wild birds. It does not usually infect humans, but some cases have been reported.
An island republic of the West Indies. Its capital is Roseau. It was discovered in 1493 by Columbus and held at different times by the French and the British in the 18th century. A member of the West Indies Federation, it achieved internal self-government in 1967 but became independent in 1978. It was named by Columbus who discovered it on Sunday, Domingo in Spanish, from the Latin Dominica dies, the Lord's Day. (From Webster's New Geographical Dictionary, 1988, p338 & Room, Brewer's Dictionary of Names, 1992, p151)
Classes of retroviruses for which monkeys or apes are hosts. Those isolated from the West African green monkey and the Asian rhesus macaque monkey are of particular interest because of their similarities to viruses causing cancer and acquired immunodeficiency syndrome (AIDS) in humans.
A genus of Old World monkeys of the subfamily CERCOPITHECINAE, family CERCOPITHECIDAE, that inhabits the mountainous regions of Ethiopia. The genus consists of only one species, Theropithecus gelada.

Gene expression profiles in HTLV-I-immortalized T cells: deregulated expression of genes involved in apoptosis regulation. (1/1876)

Human T-cell leukemia virus type I (HTLV-I) is the etiologic agent of adult T-cell leukemia, an acute and often fatal T-cell malignancy. A key step in HTLV-I-induced leukemigenesis is induction of abnormal T-cell growth and survival. Unlike antigen-stimulated T cells, which cease proliferation after a finite number of cell division, HTLV-I-infected T cells proliferate indefinitely (immortalized), thus facilitating occurrence of secondary genetic changes leading to malignant transformation. To explore the molecular basis of HTLV-I-induced abnormal T-cell survival, we compared the gene expression profiles of normal and HTLV-I-immortalized T cells using 'gene array'. These studies revealed a strikingly altered expression pattern of a large number of genes along with HTLV-I-mediated T-cell immortalization. Interestingly, many of these deregulated genes are involved in the control of programmed cell death or apoptosis. These findings indicate that disruption of the cellular apoptosis-regulatory network may play a role in the HTLV-I-mediated oncogenesis.  (+info)

Stabilization from autoproteolysis and kinetic characterization of the human T-cell leukemia virus type 1 proteinase. (2/1876)

We have developed a system for expression and purification of wild-type human T-cell leukemia virus type 1 (HTLV-1) proteinase to attain sufficient quantities for structural, kinetic, and biophysical investigations. However, similar to the human immunodeficiency virus type 1 (HIV-1) proteinase, HTLV-1 proteinase also undergoes autoproteolysis rapidly upon renaturation to produce two products. The site of this autoproteolytic cleavage was mapped, and a resistant HTLV-1 proteinase construct (L40I) as well as another construct, wherein the two cysteine residues were exchanged to alanines, were expressed and purified. Oligopeptide substrates representing the naturally occurring cleavage sites in HTLV-1 were good substrates of the HTLV-1 proteinase. The kinetic parameters kcat and Km were nearly identical for all the three enzymes. Although three of four peptides representing HTLV-1 proteinase cleavage sites were fairly good substrates of HIV-1 proteinase, only two of nine peptides representing HIV-1 proteinase cleavage sites were hydrolyzed by the HTLV-1 proteinase, suggesting substantial differences in the specificity of the two enzymes. The large difference in the specificity of the two enzymes was also demonstrated by inhibition studies. Of the several inhibitors of HIV-1 or other retroviral proteinases that were tested on HTLV-1 proteinase, only two inhibit the enzyme with a Ki lower than 100 nM.  (+info)

Binding of c-Rel to STAT5 target sequences in HTLV-I-transformed T cells. (3/1876)

The type I human T-cell leukemia virus (HTLV-I) induces abnormal growth and subsequent transformation of T cells, which is associated with the development of an acute T-cell malignancy termed adult T-cell leukemia. A characteristic of HTLV-I-transformed T cells is the constitutive nuclear expression of NF-kappaB/Rel family of transcription factors, which appears to be essential for the growth of these transformed cells. Although NF-kappaB/Rel factors are known to induce the expression of T-cell growth factor interleukin (IL)-2, it is unclear how they participate in the IL-2-independent growth of HTLV-I-transformed cells. In this study, we show that certain NF-kappaB/Rel members, predominantly c-Rel, interact with enhancer sequences for STAT5, a key transcription factor mediating IL-2-induced T-cell proliferation. Reporter gene assays reveal that the binding of c-Rel to the STAT5 site present in the Fc gammaR1 gene leads to potent transactivation of this enhancer. Binding of c-Rel to the Fc gammaR1 STAT site also occurs in human peripheral blood T cells immortalized with HTLV-I in vitro and is correlated with enhanced levels of proliferation of these cells. These results raise the possibility that NF-kappaB/Rel may participate in the growth control of HTLV-I-transformed T cells by regulating genes driven by both kappaB and certain STAT enhancers.  (+info)

Two types of HTLV-1 particles are released from MT-2 cells. (4/1876)

The MT-2 cell line transformed by human T-cell leukemia virus type 1 (HTLV-1) contains one complete provirus and seven defective proviruses. Four defective genomes have an identical structure (LTR-MA-deltaCA-pX-LTR) with an open reading frame that spans from MA to pX, giving rise to a 3.4-kb (24S) RNA transcript encoding a chimeric Gag-pX protein, p28. MT-2 cells release two distinct types of virions. The major "classic" type of particle has a buoyant density of 1.155-1.16 g/cm3 and contains the standard HTLV-I structural proteins and reverse transcriptase (RT). In addition, about 5% of particles are "light," approximately 1.12 g/cm3, and contain p28, RT activity, and the 3.4-kb RNA transcript. RT-PCR and in vitro translation indicate that some of the classic HTLV-1 particles package 3.4-kb RNA as well as full-length 8.5-kb RNA. In addition to matrix features, the p28 protein has a motif resembling a zinc finger at the C-terminal, pX0 region, which may play a role in the assembly of the defective light virions.  (+info)

The human T cell leukemia virus type I-tax gene is responsible for the development of both inflammatory polyarthropathy resembling rheumatoid arthritis and noninflammatory ankylotic arthropathy in transgenic mice. (5/1876)

We previously reported that inflammatory arthropathy resembling rheumatoid arthritis (RA) develops among transgenic mice carrying the long terminal repeat (LTR)-env-pX-LTR region of human T cell leukemia virus type I (LTR-pX-Tg mice). Because four genes are encoded in this region, we produced transgenic mice that only express the tax gene to examine its role in the development of arthritis. Transgenic mice were produced by constructing DNAs that express the tax gene alone under the control of either its own LTR or CD4 enhancer/promoter and by microinjecting them into C3H/HeN-fertilized ova. We produced seven transgenic mice carrying the LTR-tax gene and nine mice carrying the CD4-tax and found that one of the LTR-tax-Tg mice and five of CD4-tax-Tg mice developed RA-like inflammatory arthropathy similar to LTR-pX-Tg mice, indicating that the tax gene is arthritogenic. On the other hand, the other two LTR-tax-Tg mice had ankylotic changes caused by new bone formation without inflammation. In these ankylotic mice, tax mRNA, inflammatory cytokine mRNA, and autoantibody levels except for TGF-beta1 level were lower than those in LTR-pX- or CD4-tax-Tg mice. These results show that Tax is responsible for the development of inflammatory arthropathy resembling RA and that this protein also causes ankylotic arthropathy.  (+info)

Interaction of Gli2 with CREB protein on DNA elements in the long terminal repeat of human T-cell leukemia virus type 1 is responsible for transcriptional activation by tax protein. (6/1876)

The long terminal repeat (LTR) of human T-cell leukemia virus type 1 (HTLV-1) has two distinct DNA elements, one copy of TRE2S and three copies of a 21-bp sequence that respond to the viral trans-activator protein, Tax. Either multiple copies of the 21-bp sequence or a combination of one copy each of TRE2S and 21-bp sequence is required for efficient trans activation by Tax. In the trans activation of multiple copies of 21-bp sequence, CREB/ATF protein plays an essential role in forming a complex with Tax. To understand the role of TRE2S in trans activation of one copy of 21-bp sequence, we examined protein binding to the DNA elements by DNA affinity precipitation assay including Gli2 protein binding to TRE2S and CREB protein binding to 21-bp sequence. Binding of CREB to a DNA probe containing both elements, TRE2S-21bp probe, was dependent on Gli2 protein under restricted conditions and was enhanced in a dose-dependent fashion by the binding of Gli2 protein to the same probe. Mutation in either element abolished the efficient binding of CREB. A glutathione S-transferase fusion protein of a fragment of Gli2 was able to bind to CREB. Therefore, Gli2-CREB interaction on the DNA probe is proposed to stabilize CREB binding to DNA. Tax can bind to CREB protein on the DNA; therefore, stabilization of DNA binding of CREB results in more recruitment of Tax onto DNA. Conversely, Tax increased the DNA binding of CREB, although it had almost no effect on the binding of Gli2. These results suggest that Gli2 binds to the DNA element and interacts with CREB, resulting in more recruitment of Tax, which in turn stabilizes DNA binding of CREB. Similar cooperation of the protein binding to TRE2S-21bp probe was also observed in nuclear extract of an HTLV-1-infected T-cell line. Consistent with the Gli2-CREB interaction on the DNA elements, Tax-mediated trans activation was dependent on the size of the spacer between TRE2S and 21-bp sequence. The effective sizes of the spacer suggest that TRE2S in the LTR would cooperate with the second and third copies of the 21-bp sequence and contribute to trans activation of the viral gene transcription.  (+info)

Human T-cell leukemia retrovirus-Tax protein is a repressor of nuclear receptor signaling. (7/1876)

The Tax oncoprotein promotes cellular transformation and is associated with the pathogenesis of adult T-cell leukemia. Tax expression activates transcription via the cAMP enhancer binding protein/activating transcription factor (CREB/ATF) and NF-kappaB pathways. In contrast to its positive action, here we demonstrate that Tax is a potent repressor of steroid and retinoid receptor transcription. The Tax protein becomes localized in the promyelocytic (PML) oncogenic domain, and unexpectedly, expression of the PML protein reverses Tax-induced repression. These results suggest that PML and Tax may act in opposing manners to influence nuclear receptor transcription and human T-cell leukemia retrovirus pathogenesis.  (+info)

Constitutive activation of NF-kappaB in primary adult T-cell leukemia cells. (8/1876)

Human T-cell leukemia virus type I (HTLV-I) is an etiologic agent of adult T-cell leukemia (ATL). The viral protein Tax induces the activation and nuclear translocalization of transcription factor NF-kappaB, which is proposed to play a crucial role in the transformation of T cells by HTLV-I. However, the HTLV-I genes including Tax are not expressed significantly in primary leukemic cells from ATL patients. In this study, we examined the basis for NF-kappaB activation in freshly isolated leukemic cells from ATL patients. We found that leukemic cells from ATL patients, like HTLV-I-infected T-cell lines, display constitutive NF-kappaB DNA binding activity and increased degradation of IkappaBalpha (an inhibitor of NF-kappaB). Whereas the NF-kappaB binding activity in Tax-expressing T-cell lines consisted mostly of p50/c-Rel, fresh ATL samples contained p50/p50 and p50/p65 heterodimers. One T-cell line derived from ATL leukemic cells, TL-Om1, displayed constitutive NF-kappaB activity, as well as enhanced degradation of IkappaBalpha, despite the lack of detectable Tax expression. Interestingly, the NF-kappaB in TL-Om1 consists of p50/p50 and p50/p65 like that in fresh primary leukemic cells. Our results suggest that activation of NF-kappaB occurs through a Tax-independent mechanism in leukemic cells of ATL patients, possibly due to differential NF-kappaB subunit activation.  (+info)

HTLV-I (Human T-lymphotropic virus type 1) infection is a viral infection that attacks the CD4+ T-cells (a type of white blood cell) and can lead to the development of various diseases, including Adult T-cell Leukemia/Lymphoma (ATLL) and HTLV-I Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP). The virus is primarily transmitted through breastfeeding, sexual contact, or contaminated blood products. After infection, the virus becomes integrated into the host's DNA and can remain dormant for years, even decades, before leading to the development of disease. Most people infected with HTLV-I do not develop any symptoms, but a small percentage will go on to develop serious complications.

Human T-lymphotropic virus 1 (HTLV-1) is a complex retrovirus that infects CD4+ T lymphocytes and can cause adult T-cell leukemia/lymphoma (ATLL) and HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). The virus is primarily transmitted through breastfeeding, sexual contact, or contaminated blood products. After infection, the virus integrates into the host's genome and can remain latent for years or even decades before leading to disease. HTLV-1 is endemic in certain regions of the world, including Japan, the Caribbean, Central and South America, and parts of Africa.

Tropical spastic paraparesis (TSP) is a type of myelopathy (spinal cord disorder) that is associated with chronic infectious or inflammatory conditions. The term "paraparesis" refers to partial weakness in the lower extremities, which is a characteristic feature of TSP.

In Tropical spastic paraparesis, there is a slow and progressive degeneration of the spinal cord, leading to symptoms such as muscle weakness, stiffness, and spasticity (involuntary muscle contractions) in the legs. Other common symptoms include sensory loss, bladder and bowel dysfunction, and sexual impairment.

TSP is often caused by a chronic infection with the human T-lymphotropic virus type 1 (HTLV-1), which is endemic in certain tropical and subtropical regions, including the Caribbean, South America, Central America, Africa, and parts of Asia. The virus is transmitted through blood transfusions, sexual contact, and breastfeeding.

There is no cure for TSP, but symptoms can be managed with physical therapy, medications to relieve muscle spasticity, and other supportive measures. It is important to diagnose and treat TSP early to prevent or slow down the progression of the disease and improve quality of life.

HTLV-II (Human T-lymphotropic virus type 2) infection is a condition caused by the retrovirus HTLV- II. This virus primarily infects CD4+ T cells and can lead to the development of several diseases, including adult T-cell leukemia/lymphoma (ATLL), a malignancy of CD4+ T cells, and tropical spastic paraparesis/HTLV-associated myelopathy (TSP/HAM), a neurological disorder characterized by progressive weakness and stiffness in the lower extremities. However, the majority of people infected with HTLV-II remain asymptomatic throughout their lives. The virus is primarily transmitted through blood transfusions, sharing of needles, sexual contact, and from mother to child during breastfeeding.

HTLV-I antibodies are proteins produced by the immune system in response to the presence of Human T-cell Leukemia Virus type I (HTLV-I) antigens. These antibodies indicate a past or present infection with HTLV-I, which is a retrovirus that can cause adult T-cell leukemia/lymphoma and tropical spastic paraparesis/myelopathy. Detection of HTLV-I antibodies in the blood is typically done through serological tests such as ELISA and Western blot.

I'm sorry for any confusion, but "Jamaica" is not a medical term. It is a country located in the Caribbean Sea, known for its beautiful beaches, vibrant culture, and as the birthplace of reggae music. If you have any questions about medical terms or concepts, I would be happy to help answer those!

Human T-lymphotropic virus 2 (HTLV-2) is a retrovirus that primarily infects CD4+ T lymphocytes and other cells of the immune system. It is a deltaretrovirus closely related to HTLV-1, but with distinct biological properties and geographic distribution.

HTLV-2 infection is usually asymptomatic, although some individuals may develop neurological or skin disorders. However, the association between HTLV-2 and these diseases is not as clear as it is for HTLV-1 and adult T-cell leukemia/lymphoma or tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM).

HTLV-2 is primarily transmitted through breastfeeding, sexual contact, and sharing of needles among injecting drug users. It is endemic in certain populations, particularly indigenous communities in the Americas, such as the Guaraní and Kayapó in Brazil, and the Navajo and Pima in the United States. Prevalence rates can reach up to 30% in some of these populations.

There is currently no vaccine or specific treatment for HTLV-2 infection, and prevention efforts focus on reducing transmission risks through education and harm reduction strategies.

A gene product is the biochemical material, such as a protein or RNA, that is produced by the expression of a gene. Gene products are the result of the translation and transcription of genetic information encoded in DNA or RNA.

In the context of "tax," this term is not typically used in a medical definition of gene products. However, it may refer to the concept of taxing or regulating gene products in the context of genetic engineering or synthetic biology. This could involve imposing fees or restrictions on the production, use, or sale of certain gene products, particularly those that are genetically modified or engineered. The regulation of gene products is an important aspect of ensuring their safe and effective use in various applications, including medical treatments, agricultural production, and industrial processes.

Deltaretroviruses are a genus of retroviruses that include human T-lymphotropic virus (HTLV) types 1 and 2, bovine leukemia virus (BLV), and simian T-lymphotropic viruses. These viruses are characterized by their ability to cause persistent infections and can lead to the development of various diseases such as adult T-cell leukemia/lymphoma (ATLL) and tropical spastic paraparesis/HTLV-associated myelopathy (TSP/HAM).

The genome of deltaretroviruses contains two copies of single-stranded RNA, which are reverse transcribed into double-stranded DNA during the replication process. The viral DNA is then integrated into the host cell's genome, leading to a lifelong infection.

Deltaretroviruses primarily infect CD4+ T cells and other immune cells, and transmission typically occurs through bodily fluids such as breast milk, blood, and sexual contact. Prevention measures include avoiding high-risk behaviors, screening blood products, and implementing strict infection control practices in healthcare settings.

A provirus is a form of the genetic material of a retrovirus that is integrated into the DNA of the host cell it has infected. Once integrated, the provirus is replicated along with the host's own DNA every time the cell divides, and it becomes a permanent part of the host's genome.

The process of integration involves the reverse transcription of the retroviral RNA genome into DNA by the enzyme reverse transcriptase, followed by the integration of the resulting double-stranded proviral DNA into the host chromosome by the enzyme integrase.

Proviruses can remain dormant and inactive for long periods of time, or they can become active and produce new viral particles that can infect other cells. In some cases, proviruses can also disrupt the normal functioning of host genes, leading to various diseases such as cancer.

Deltaretroviruses are a genus of retroviruses that can cause chronic infections in humans and animals. The two main deltaretroviruses that infect humans are the Human T-cell Leukemia Virus type 1 (HTLV-1) and Human T-cell Leukemia Virus type 2 (HTLV-2).

HTLV-1 is primarily transmitted through breastfeeding, sexual contact, and contaminated blood products. It can cause several diseases, including Adult T-cell Leukemia/Lymphoma (ATLL) and a neurological disorder called HTLV-1 Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP).

HTLV-2 is primarily transmitted through intravenous drug use and sexual contact. While it has been associated with some diseases, such as neurological disorders and rare cases of leukemia, the link between HTLV-2 and disease is not as clear as it is for HTLV-1.

Deltaretrovirus infections can be diagnosed through blood tests that detect antibodies to the viruses or through genetic testing to detect the virus itself. There is currently no cure for deltaretrovirus infections, but antiretroviral therapy (ART) may help manage the infection and reduce the risk of transmission.

It's important to note that deltaretrovirus infections are relatively rare, and most people who are infected do not develop symptoms or disease. However, if you believe you may have been exposed to these viruses, it is important to speak with a healthcare provider for further evaluation and testing.

A carrier state is a condition in which a person carries and may be able to transmit a genetic disorder or infectious disease, but does not show any symptoms of the disease themselves. This occurs when an individual has a recessive allele for a genetic disorder or is infected with a pathogen, but does not have the necessary combination of genes or other factors required to develop the full-blown disease.

For example, in the case of cystic fibrosis, which is caused by mutations in the CFTR gene, a person who carries one normal allele and one mutated allele for the disease is considered a carrier. They do not have symptoms of cystic fibrosis themselves, but they can pass the mutated allele on to their offspring, who may then develop the disease if they inherit the mutation from both parents.

Similarly, in the case of infectious diseases, a person who is infected with a pathogen but does not show any symptoms may still be able to transmit the infection to others. This is known as being an asymptomatic carrier or a healthy carrier. For example, some people who are infected with hepatitis B virus (HBV) may not develop any symptoms of liver disease, but they can still transmit the virus to others through contact with their blood or other bodily fluids.

It's important to note that in some cases, carriers of certain genetic disorders or infectious diseases may have mild or atypical symptoms that do not meet the full criteria for a diagnosis of the disease. In these cases, they may be considered to have a "reduced penetrance" or "incomplete expression" of the disorder or infection.

I'm sorry for the confusion, but "pX" is not a standard term in genetics or genomic medicine. It may be a typo or a specific shorthand used in certain contexts. If you could provide more context or clarify what "pX" is intended to represent, I would be happy to help further.

In general, genes are segments of DNA that contain the instructions for making proteins or RNA molecules. These instructions are encoded in a genetic alphabet consisting of four nucleotide bases: adenine (A), guanine (G), cytosine (C), and thymine (T). The sequence of these bases determines the genetic information within a gene, which can vary among individuals and contribute to differences in traits and disease susceptibility.

Adult T-cell Leukemia/Lymphoma (ATLL) is a rare and aggressive type of cancer that affects the circulating white blood cells called T-lymphocytes or T-cells. It is caused by the human T-cell leukemia virus type 1 (HTLV-1), which infects CD4+ T-cells and leads to their malignant transformation. The disease can present as either acute or chronic leukemia, or as lymphoma, depending on the clinical features and laboratory findings.

The acute form of ATLL is characterized by the rapid proliferation of abnormal T-cells in the blood, bone marrow, and other organs. Patients with acute ATLL typically have a poor prognosis, with a median survival of only a few months. Symptoms may include skin rashes, lymphadenopathy (swollen lymph nodes), hepatosplenomegaly (enlarged liver and spleen), and hypercalcemia (high levels of calcium in the blood).

The chronic form of ATLL is less aggressive than the acute form, but it can still lead to serious complications. Chronic ATLL is characterized by the accumulation of abnormal T-cells in the blood and lymph nodes, as well as skin lesions and hypercalcemia. The median survival for patients with chronic ATLL is around two years.

ATLL can also present as a lymphoma, which is characterized by the proliferation of abnormal T-cells in the lymph nodes, spleen, and other organs. Lymphoma may occur in isolation or in combination with leukemic features.

The diagnosis of ATLL is based on clinical findings, laboratory tests, and the detection of HTLV-1 antibodies or proviral DNA in the blood or tissue samples. Treatment options for ATLL include chemotherapy, antiretroviral therapy, immunotherapy, and stem cell transplantation. The choice of treatment depends on several factors, including the patient's age, overall health, and the stage and type of ATLL.

Viral load refers to the amount or quantity of virus (like HIV, Hepatitis C, SARS-CoV-2) present in an individual's blood or bodily fluids. It is often expressed as the number of virus copies per milliliter of blood or fluid. Monitoring viral load is important in managing and treating certain viral infections, as a higher viral load may indicate increased infectivity, disease progression, or response to treatment.

Mononuclear leukocytes are a type of white blood cells (leukocytes) that have a single, large nucleus. They include lymphocytes (B-cells, T-cells, and natural killer cells), monocytes, and dendritic cells. These cells play important roles in the body's immune system, including defending against infection and disease, and participating in immune responses and surveillance. Mononuclear leukocytes can be found in the bloodstream as well as in tissues throughout the body. They are involved in both innate and adaptive immunity, providing specific and nonspecific defense mechanisms to protect the body from harmful pathogens and other threats.

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

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

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

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

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

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

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

Viral DNA refers to the genetic material present in viruses that consist of DNA as their core component. Deoxyribonucleic acid (DNA) is one of the two types of nucleic acids that are responsible for storing and transmitting genetic information in living organisms. Viruses are infectious agents much smaller than bacteria that can only replicate inside the cells of other organisms, called hosts.

Viral DNA can be double-stranded (dsDNA) or single-stranded (ssDNA), depending on the type of virus. Double-stranded DNA viruses have a genome made up of two complementary strands of DNA, while single-stranded DNA viruses contain only one strand of DNA.

Examples of dsDNA viruses include Adenoviruses, Herpesviruses, and Poxviruses, while ssDNA viruses include Parvoviruses and Circoviruses. Viral DNA plays a crucial role in the replication cycle of the virus, encoding for various proteins necessary for its multiplication and survival within the host cell.

I'm sorry for any confusion, but "Japan" is not a medical term. Japan is the name of a country, officially known as Nippon-koku or Nihon-koku in Japanese, and is located in East Asia. It is an island nation in the Pacific Ocean with a population of about 126 million people.

If you have any medical questions or terms that you would like me to define, please let me know!

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

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

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

Acquired Immunodeficiency Syndrome (AIDS) is a chronic, life-threatening condition caused by the Human Immunodeficiency Virus (HIV). AIDS is the most advanced stage of HIV infection, characterized by the significant weakening of the immune system, making the person more susceptible to various opportunistic infections and cancers.

The medical definition of AIDS includes specific criteria based on CD4+ T-cell count or the presence of certain opportunistic infections and diseases. According to the Centers for Disease Control and Prevention (CDC), a person with HIV is diagnosed with AIDS when:

1. The CD4+ T-cell count falls below 200 cells per cubic millimeter of blood (mm3) - a normal range is typically between 500 and 1,600 cells/mm3.
2. They develop one or more opportunistic infections or cancers that are indicative of advanced HIV disease, regardless of their CD4+ T-cell count.

Some examples of these opportunistic infections and cancers include:

* Pneumocystis pneumonia (PCP)
* Candidiasis (thrush) affecting the esophagus, trachea, or lungs
* Cryptococcal meningitis
* Toxoplasmosis of the brain
* Cytomegalovirus disease
* Kaposi's sarcoma
* Non-Hodgkin's lymphoma
* Invasive cervical cancer

It is important to note that with appropriate antiretroviral therapy (ART), people living with HIV can maintain their CD4+ T-cell counts, suppress viral replication, and prevent the progression to AIDS. Early diagnosis and consistent treatment are crucial for managing HIV and improving life expectancy and quality of life.

Deltaretroviruses are a genus of retroviruses that include human T-lymphotropic virus (HTLV) types 1 and 2, bovine leukemia virus (BLV), and simian T-lymphotropic viruses. Antibodies against deltaretroviruses are proteins produced by the immune system in response to an infection with one of these viruses.

Antibodies are formed when the immune system recognizes a foreign substance, such as a virus, as harmful. The immune system then produces specific proteins called antibodies to bind to and help neutralize or remove the foreign substance from the body. Detection of deltaretrovirus antibodies in an individual's blood can indicate a current or past infection with one of these viruses.

It is important to note that the presence of deltaretrovirus antibodies does not necessarily mean that the person has symptoms or will develop disease related to the virus. Some people with deltaretrovirus antibodies may never develop symptoms, while others may develop serious illnesses such as adult T-cell leukemia/lymphoma (HTLV-1) or neurological disorders (HTLV-1 associated myelopathy/tropical spastic paraparesis).

If you suspect that you may have been exposed to a deltaretrovirus, it is important to speak with your healthcare provider for further evaluation and testing.

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

Simian T-lymphotropic virus 1 (STLV-1) is a retrovirus that primarily infects Asian monkeys and apes. It is closely related to the human T-lymphotropic virus type 1 (HTLV-1), and there is evidence to suggest that STLV-1 may have been transmitted to humans through close contact with infected non-human primates, resulting in the emergence of HTLV-1.

Like HTLV-1, STLV-1 primarily infects CD4+ T lymphocytes and can cause a persistent infection. However, unlike HTLV-1, which is associated with several diseases including adult T-cell leukemia/lymphoma and tropical spastic paraparesis/HTLV-1-associated myelopathy (TSP/HAM), STLV-1 has not been definitively linked to any specific human diseases.

STLV-1 infection is typically asymptomatic in both monkeys and humans, but it can cause a range of clinical manifestations in some individuals, including lymphadenopathy, hepatitis, and neurological symptoms. The virus is primarily transmitted through contact with infected bodily fluids, such as blood, breast milk, and semen.

Research on STLV-1 is important for understanding the evolution and epidemiology of retroviruses, as well as for developing strategies to prevent transmission and manage related diseases in both humans and non-human primates.

HTLV-II antibodies are proteins produced by the immune system in response to the presence of Human T-lymphotropic Virus type II (HTLV-II) in the body. HTLV-II is a retrovirus that can cause chronic infection and is associated with certain diseases, such as adult T-cell leukemia/lymphoma and myelopathy/tropical spastic paraparesis. The detection of HTLV-II antibodies in the blood indicates exposure to the virus, but not all infected individuals will develop symptoms or disease.

Polymerase Chain Reaction (PCR) is a laboratory technique used to amplify specific regions of DNA. It enables the production of thousands to millions of copies of a particular DNA sequence in a rapid and efficient manner, making it an essential tool in various fields such as molecular biology, medical diagnostics, forensic science, and research.

The PCR process involves repeated cycles of heating and cooling to separate the DNA strands, allow primers (short sequences of single-stranded DNA) to attach to the target regions, and extend these primers using an enzyme called Taq polymerase, resulting in the exponential amplification of the desired DNA segment.

In a medical context, PCR is often used for detecting and quantifying specific pathogens (viruses, bacteria, fungi, or parasites) in clinical samples, identifying genetic mutations or polymorphisms associated with diseases, monitoring disease progression, and evaluating treatment effectiveness.

Messenger RNA (mRNA) is a type of RNA (ribonucleic acid) that carries genetic information copied from DNA in the form of a series of three-base code "words," each of which specifies a particular amino acid. This information is used by the cell's machinery to construct proteins, a process known as translation. After being transcribed from DNA, mRNA travels out of the nucleus to the ribosomes in the cytoplasm where protein synthesis occurs. Once the protein has been synthesized, the mRNA may be degraded and recycled. Post-transcriptional modifications can also occur to mRNA, such as alternative splicing and addition of a 5' cap and a poly(A) tail, which can affect its stability, localization, and translation efficiency.

Deltaretroviruses are a genus of retroviruses that include human T-lymphotropic virus (HTLV) types 1 and 2, bovine leukemia virus (BLV), and simian T-lymphotropic viruses. These viruses are characterized by the presence of the unique region (U) in their genome, which encodes several accessory proteins, including Tax, Rex, p12, p30, and p13.

Deltaretrovirus antigens refer to the proteins expressed by these viruses that can stimulate an immune response in infected individuals. The two main antigens of deltaretroviruses are:

1. Environmental Response Factor (ERF): Also known as p12 or p13, this protein is involved in viral replication and infectivity. It has been shown to induce the production of antibodies in infected individuals.
2. Transactivator X (Tax): This protein is a potent transcriptional activator that regulates viral gene expression and host cell signaling pathways. Tax is a major target of cytotoxic T lymphocytes (CTLs) and has been implicated in the development of HTLV-associated diseases such as adult T-cell leukemia/lymphoma (ATLL) and tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM).

Detection of deltaretrovirus antigens in clinical samples can be used for diagnosis, prognosis, and monitoring of HTLV and BLV infections. However, the interpretation of these assays should be done with caution, as the presence of antibodies or CTLs against these antigens does not necessarily indicate active infection or disease.

Primate T-lymphotropic virus 3 (PTLV-3) is not a widely recognized or established medical term. However, it's possible that you are referring to Primate T-cell Leukemia Virus type 3 (PTLV-3), which is a retrovirus that primarily infects non-human primates. It is closely related to the human T-lymphotropic virus type 1 and 2 (HTLV-1 and HTLV-2). PTLV-3, like other T-cell leukemia viruses, has been associated with the development of certain types of cancer, particularly adult T-cell leukemia/lymphoma (ATLL) in its natural host species. However, there is no known human infection with PTLV-3 to date.

Retroviridae proteins, oncogenic, refer to the proteins expressed by retroviruses that have the ability to transform normal cells into cancerous ones. These oncogenic proteins are typically encoded by viral genes known as "oncogenes," which are acquired through the process of transduction from the host cell's DNA during retroviral replication.

The most well-known example of an oncogenic retrovirus is the Human T-cell Leukemia Virus Type 1 (HTLV-1), which encodes the Tax and HBZ oncoproteins. These proteins manipulate various cellular signaling pathways, leading to uncontrolled cell growth and malignant transformation.

It is important to note that not all retroviruses are oncogenic, and only a small subset of them have been associated with cancer development in humans or animals.

HTLV-I (Human T-lymphotropic virus type I) antigens are proteins expressed by the HTLV-I virus, which can be detected in an infected individual's serum. The two main types of HTLV-I antigens are:

1. Core antigen (p24): This is a structural protein present in the viral core. Detection of p24 antigen in the blood indicates active viral replication.

2. Surface envelope glycoprotein (gp46): This antigen is found on the surface of the virus and plays a role in the attachment and entry of the virus into host cells.

The detection of HTLV-I antigens can be used for diagnostic purposes, particularly in serological tests such as ELISA or Western blot assays, to identify individuals who have been infected with the virus.

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

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

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

HTLV-II (Human T-lymphotropic virus type 2) antigens refer to specific proteins found on the surface of the virus that can stimulate an immune response in an infected individual. These antigens are typically used in laboratory tests, such as ELISA or Western blot assays, to detect the presence of antibodies produced by the host's immune system in response to the infection.

The two main HTLV-II antigens used in these tests are the envelope protein (gp46) and the core protein (p24). The gp46 protein is a transmembrane glycoprotein located on the viral envelope, while p24 is a capsid protein found inside the virus. Detection of antibodies against these antigens indicates current or past infection with HTLV-II. However, it's important to note that not all infected individuals will develop detectable antibodies, and further testing may be required for confirmation.

I'm sorry for any confusion, but "French Guiana" is not a medical term or concept. It's a geographical location, specifically an overseas department and region of France, located on the northeastern coast of South America. If you have any questions about geographical places, I'd be happy to try to help answer those, but for medical inquiries, please provide a medical term or concept and I will do my best to provide a definition or explanation.

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

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

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

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

T-lymphocyte subsets refer to distinct populations of T-cells, which are a type of white blood cell that plays a central role in cell-mediated immunity. The two main types of T-lymphocytes are CD4+ and CD8+ cells, which are defined by the presence or absence of specific proteins called cluster differentiation (CD) molecules on their surface.

CD4+ T-cells, also known as helper T-cells, play a crucial role in activating other immune cells, such as B-lymphocytes and macrophages, to mount an immune response against pathogens. They also produce cytokines that help regulate the immune response.

CD8+ T-cells, also known as cytotoxic T-cells, directly kill infected cells or tumor cells by releasing toxic substances such as perforins and granzymes.

The balance between these two subsets of T-cells is critical for maintaining immune homeostasis and mounting effective immune responses against pathogens while avoiding excessive inflammation and autoimmunity. Therefore, the measurement of T-lymphocyte subsets is essential in diagnosing and monitoring various immunological disorders, including HIV infection, cancer, and autoimmune diseases.

A gene product is the biochemical material, such as a protein or RNA, that is produced by the expression of a gene. Env, short for "envelope," refers to a type of gene product that is commonly found in enveloped viruses. The env gene encodes the viral envelope proteins, which are crucial for the virus's ability to attach to and enter host cells during infection. These envelope proteins typically form a coat around the exterior of the virus and interact with receptors on the surface of the host cell, triggering the fusion or endocytosis processes that allow the viral genome to enter the host cell.

Therefore, in medical terms, 'Gene Products, env' specifically refers to the proteins or RNA produced by the env gene in enveloped viruses, which play a critical role in the virus's infectivity and pathogenesis.

RNA viruses are a type of virus that contain ribonucleic acid (RNA) as their genetic material, as opposed to deoxyribonucleic acid (DNA). RNA viruses replicate by using an enzyme called RNA-dependent RNA polymerase to transcribe and replicate their RNA genome.

There are several different groups of RNA viruses, including:

1. Negative-sense single-stranded RNA viruses: These viruses have a genome that is complementary to the mRNA and must undergo transcription to produce mRNA before translation can occur. Examples include influenza virus, measles virus, and rabies virus.
2. Positive-sense single-stranded RNA viruses: These viruses have a genome that can serve as mRNA and can be directly translated into protein after entry into the host cell. Examples include poliovirus, rhinoviruses, and coronaviruses.
3. Double-stranded RNA viruses: These viruses have a genome consisting of double-stranded RNA and use a complex replication strategy involving both transcription and reverse transcription. Examples include rotaviruses and reoviruses.

RNA viruses are known to cause a wide range of human diseases, ranging from the common cold to more severe illnesses such as hepatitis C, polio, and COVID-19. Due to their high mutation rates and ability to adapt quickly to new environments, RNA viruses can be difficult to control and treat with antiviral drugs or vaccines.

"Cercocebus" is a genus of Old World monkeys that includes several species, such as the sooty mangabey and the gray-cheeked mangabey. These monkeys are native to central Africa and are known for their distinctive appearance, with a long tail, dark fur, and light cheek whiskers. They are omnivorous and live in social groups. The name "Cercocebus" comes from the Greek words "kerkos," meaning tail, and "kephale," meaning head, referring to their long tails.

Virus replication is the process by which a virus produces copies or reproduces itself inside a host cell. This involves several steps:

1. Attachment: The virus attaches to a specific receptor on the surface of the host cell.
2. Penetration: The viral genetic material enters the host cell, either by invagination of the cell membrane or endocytosis.
3. Uncoating: The viral genetic material is released from its protective coat (capsid) inside the host cell.
4. Replication: The viral genetic material uses the host cell's machinery to produce new viral components, such as proteins and nucleic acids.
5. Assembly: The newly synthesized viral components are assembled into new virus particles.
6. Release: The newly formed viruses are released from the host cell, often through lysis (breaking) of the cell membrane or by budding off the cell membrane.

The specific mechanisms and details of virus replication can vary depending on the type of virus. Some viruses, such as DNA viruses, use the host cell's DNA polymerase to replicate their genetic material, while others, such as RNA viruses, use their own RNA-dependent RNA polymerase or reverse transcriptase enzymes. Understanding the process of virus replication is important for developing antiviral therapies and vaccines.

I'm happy to help! However, I believe there might be a slight mistake in your question. "Gene products" is a general term that refers to the molecules produced by genes, including both RNA and proteins. On the other hand, "rex" is often used as an abbreviation for "regulated expression," which can be a part of a gene's name indicating its regulatory properties.

If you are referring to a specific genetic element or molecule named "rex," I would need more context or information to provide an accurate medical definition. Nonetheless, I hope this initial explanation helps! If you have further questions or need clarification, please let me know.

Vaccinia virus is a large, complex DNA virus that belongs to the Poxviridae family. It is the virus used in the production of the smallpox vaccine. The vaccinia virus is not identical to the variola virus, which causes smallpox, but it is closely related and provides cross-protection against smallpox infection.

The vaccinia virus has a unique replication cycle that occurs entirely in the cytoplasm of infected cells, rather than in the nucleus like many other DNA viruses. This allows the virus to evade host cell defenses and efficiently produce new virions. The virus causes the formation of pocks or lesions on the skin, which contain large numbers of virus particles that can be transmitted to others through close contact.

Vaccinia virus has also been used as a vector for the delivery of genes encoding therapeutic proteins, vaccines against other infectious diseases, and cancer therapies. However, the use of vaccinia virus as a vector is limited by its potential to cause adverse reactions in some individuals, particularly those with weakened immune systems or certain skin conditions.

Jurkat cells are a type of human immortalized T lymphocyte (a type of white blood cell) cell line that is commonly used in scientific research. They were originally isolated from the peripheral blood of a patient with acute T-cell leukemia. Jurkat cells are widely used as a model system to study T-cell activation, signal transduction, and apoptosis (programmed cell death). They are also used in the study of HIV infection and replication, as they can be infected with the virus and used to investigate viral replication and host cell responses.

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

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

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

Leukemia, T-cell is a type of cancer that affects the T-cells or T-lymphocytes, which are a type of white blood cells responsible for cell-mediated immunity. It is characterized by an excessive and uncontrolled production of abnormal T-cells in the bone marrow, leading to the displacement of healthy cells and impairing the body's ability to fight infections and regulate immune responses.

T-cell leukemia can be acute or chronic, depending on the rate at which the disease progresses. Acute T-cell leukemia progresses rapidly, while chronic T-cell leukemia has a slower course of progression. Symptoms may include fatigue, fever, frequent infections, weight loss, easy bruising or bleeding, and swollen lymph nodes. Treatment typically involves chemotherapy, radiation therapy, stem cell transplantation, or targeted therapy, depending on the type and stage of the disease.

Virus receptors are specific molecules (commonly proteins) on the surface of host cells that viruses bind to in order to enter and infect those cells. This interaction between the virus and its receptor is a critical step in the infection process. Different types of viruses have different receptor requirements, and identifying these receptors can provide important insights into the biology of the virus and potential targets for antiviral therapies.

I'm sorry for any confusion, but "Melanesia" is not a medical term. It is a geographical region in the southwestern Pacific Ocean, consisting of an island group including New Guinea, the Bismarck Archipelago, the Solomon Islands, Vanuatu, New Caledonia, and the Fiji islands. The term "Melanesia" comes from the Greek words "melas," meaning black, and "nesos," meaning island, referring to the dark skin of the inhabitants. It's primarily used in anthropological, geographical, and cultural contexts.

Viral genes refer to the genetic material present in viruses that contains the information necessary for their replication and the production of viral proteins. In DNA viruses, the genetic material is composed of double-stranded or single-stranded DNA, while in RNA viruses, it is composed of single-stranded or double-stranded RNA.

Viral genes can be classified into three categories: early, late, and structural. Early genes encode proteins involved in the replication of the viral genome, modulation of host cell processes, and regulation of viral gene expression. Late genes encode structural proteins that make up the viral capsid or envelope. Some viruses also have structural genes that are expressed throughout their replication cycle.

Understanding the genetic makeup of viruses is crucial for developing antiviral therapies and vaccines. By targeting specific viral genes, researchers can develop drugs that inhibit viral replication and reduce the severity of viral infections. Additionally, knowledge of viral gene sequences can inform the development of vaccines that stimulate an immune response to specific viral proteins.

A blood donor is a person who voluntarily gives their own blood or blood components to be used for the benefit of another person in need. The blood donation process involves collecting the donor's blood, testing it for infectious diseases, and then storing it until it is needed by a patient. There are several types of blood donations, including:

1. Whole blood donation: This is the most common type of blood donation, where a donor gives one unit (about 450-500 milliliters) of whole blood. The blood is then separated into its components (red cells, plasma, and platelets) for transfusion to patients with different needs.
2. Double red cell donation: In this type of donation, the donor's blood is collected using a special machine that separates two units of red cells from the whole blood. The remaining plasma and platelets are returned to the donor during the donation process. This type of donation can be done every 112 days.
3. Platelet donation: A donor's blood is collected using a special machine that separates platelets from the whole blood. The red cells and plasma are then returned to the donor during the donation process. This type of donation can be done every seven days, up to 24 times a year.
4. Plasma donation: A donor's blood is collected using a special machine that separates plasma from the whole blood. The red cells and platelets are then returned to the donor during the donation process. This type of donation can be done every 28 days, up to 13 times a year.

Blood donors must meet certain eligibility criteria, such as being in good health, aged between 18 and 65 (in some countries, the upper age limit may vary), and weighing over 50 kg (110 lbs). Donors are also required to answer medical questionnaires and undergo a mini-physical examination before each donation. The frequency of blood donations varies depending on the type of donation and the donor's health status.

I'm sorry for any confusion, but the term "Indians, Central American" is not a medical term. It refers to individuals or populations that originate from Central America and self-identify as indigenous or native to the region. In a medical context, it's more common to see specific references to individual ethnic groups or populations, such as Maya, Garifuna, or Miskitu, among others. These groups may have unique genetic characteristics, health risks, or cultural practices that are relevant to medical care and research. However, it's important to note that any discussion of medical issues should be sensitive to the individual's self-identified ethnicity and personal preferences.

Retroviridae is a family of viruses that includes HIV (Human Immunodeficiency Virus). Retroviridae proteins refer to the various structural and functional proteins that are encoded by the retroviral genome. These proteins can be categorized into three main groups:

1. Group-specific antigen (Gag) proteins: These proteins make up the viral matrix, capsid, and nucleocapsid. They are involved in the assembly of new virus particles.

2. Polymerase (Pol) proteins: These proteins include the reverse transcriptase, integrase, and protease enzymes. Reverse transcriptase is responsible for converting the viral RNA genome into DNA, which can then be integrated into the host cell's genome by the integrase enzyme. The protease enzyme is involved in processing the polyprotein precursors of Gag and Pol into their mature forms.

3. Envelope (Env) proteins: These proteins are responsible for the attachment and fusion of the virus to the host cell membrane. They are synthesized as a precursor protein, which is then cleaved by a host cell protease to form two distinct proteins - the surface unit (SU) and the transmembrane unit (TM). The SU protein contains the receptor-binding domain, while the TM protein forms the transmembrane anchor.

Retroviral proteins play crucial roles in various stages of the viral life cycle, including entry, reverse transcription, integration, transcription, translation, assembly, and release. Understanding the functions of these proteins is essential for developing effective antiretroviral therapies and vaccines against retroviral infections.

I'm sorry for any confusion, but there seems to be no established medical definition for "Human T-lymphotropic virus 3" (HTLV-3). So far, only three types of Human T-lymphotropic viruses have been officially recognized and classified by the International Committee on Taxonomy of Viruses (ICTV). These are HTLV-1, HTLV-2, and HTLV-3/HTLV-4 provisional. The proposed HTLV-3 and HTLV-4 were identified in a few cameroonian hunters and not widely found in humans yet. Therefore, it's crucial to rely on validated and widely accepted sources when researching medical definitions and information.

Cell transformation, viral refers to the process by which a virus causes normal cells to become cancerous or tumorigenic. This occurs when the genetic material of the virus integrates into the DNA of the host cell and alters its regulation, leading to uncontrolled cell growth and division. Some viruses known to cause cell transformation include human papillomavirus (HPV), hepatitis B virus (HBV), and certain types of herpesviruses.

Virus cultivation, also known as virus isolation or viral culture, is a laboratory method used to propagate and detect viruses by introducing them to host cells and allowing them to replicate. This process helps in identifying the specific virus causing an infection and studying its characteristics, such as morphology, growth pattern, and sensitivity to antiviral agents.

The steps involved in virus cultivation typically include:

1. Collection of a clinical sample (e.g., throat swab, blood, sputum) from the patient.
2. Preparation of the sample by centrifugation or filtration to remove cellular debris and other contaminants.
3. Inoculation of the prepared sample into susceptible host cells, which can be primary cell cultures, continuous cell lines, or embryonated eggs, depending on the type of virus.
4. Incubation of the inoculated cells under appropriate conditions to allow viral replication.
5. Observation for cytopathic effects (CPE), which are changes in the host cells caused by viral replication, such as cell rounding, shrinkage, or lysis.
6. Confirmation of viral presence through additional tests, like immunofluorescence assays, polymerase chain reaction (PCR), or electron microscopy.

Virus cultivation is a valuable tool in diagnostic virology, vaccine development, and research on viral pathogenesis and host-virus interactions. However, it requires specialized equipment, trained personnel, and biosafety measures due to the potential infectivity of the viruses being cultured.

Phylogeny is the evolutionary history and relationship among biological entities, such as species or genes, based on their shared characteristics. In other words, it refers to the branching pattern of evolution that shows how various organisms have descended from a common ancestor over time. Phylogenetic analysis involves constructing a tree-like diagram called a phylogenetic tree, which depicts the inferred evolutionary relationships among organisms or genes based on molecular sequence data or other types of characters. This information is crucial for understanding the diversity and distribution of life on Earth, as well as for studying the emergence and spread of diseases.

Retroviridae infections refer to diseases caused by retroviruses, which are a type of virus that integrates its genetic material into the DNA of the host cell. This allows the virus to co-opt the cell's own machinery to produce new viral particles and infect other cells.

Some well-known retroviruses include human immunodeficiency virus (HIV), which causes AIDS, and human T-lymphotropic virus (HTLV), which can cause certain types of cancer and neurological disorders.

Retroviral infections can have a range of clinical manifestations depending on the specific virus and the host's immune response. HIV infection, for example, is characterized by progressive immunodeficiency that makes the infected individual susceptible to a wide range of opportunistic infections and cancers. HTLV infection, on the other hand, can cause adult T-cell leukemia/lymphoma or tropical spastic paraparesis, a neurological disorder.

Prevention and treatment strategies for retroviral infections depend on the specific virus but may include antiretroviral therapy (ART), vaccination, and behavioral modifications to reduce transmission risk.

HIV (Human Immunodeficiency Virus) is a species of lentivirus (a subgroup of retrovirus) that causes HIV infection and over time, HIV infection can lead to AIDS (Acquired Immunodeficiency Syndrome). This virus attacks the immune system, specifically the CD4 cells, also known as T cells, which are a type of white blood cell that helps coordinate the body's immune response. As HIV destroys these cells, the body becomes more vulnerable to other infections and diseases. It is primarily spread through bodily fluids like blood, semen, vaginal fluids, and breast milk.

It's important to note that while there is no cure for HIV, with proper medical care, HIV can be controlled. Treatment for HIV is called antiretroviral therapy (ART). If taken as prescribed, this medicine reduces the amount of HIV in the body to a very low level, which keeps the immune system working and prevents illness. This treatment also greatly reduces the risk of transmission.

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

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

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

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

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

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

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

Gene expression regulation, viral, refers to the processes that control the production of viral gene products, such as proteins and nucleic acids, during the viral life cycle. This can involve both viral and host cell factors that regulate transcription, RNA processing, translation, and post-translational modifications of viral genes.

Viral gene expression regulation is critical for the virus to replicate and produce progeny virions. Different types of viruses have evolved diverse mechanisms to regulate their gene expression, including the use of promoters, enhancers, transcription factors, RNA silencing, and epigenetic modifications. Understanding these regulatory processes can provide insights into viral pathogenesis and help in the development of antiviral therapies.

Virus shedding refers to the release of virus particles by an infected individual, who can then transmit the virus to others through various means such as respiratory droplets, fecal matter, or bodily fluids. This occurs when the virus replicates inside the host's cells and is released into the surrounding environment, where it can infect other individuals. The duration of virus shedding varies depending on the specific virus and the individual's immune response. It's important to note that some individuals may shed viruses even before they show symptoms, making infection control measures such as hand hygiene, mask-wearing, and social distancing crucial in preventing the spread of infectious diseases.

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

A viral RNA (ribonucleic acid) is the genetic material found in certain types of viruses, as opposed to viruses that contain DNA (deoxyribonucleic acid). These viruses are known as RNA viruses. The RNA can be single-stranded or double-stranded and can exist as several different forms, such as positive-sense, negative-sense, or ambisense RNA. Upon infecting a host cell, the viral RNA uses the host's cellular machinery to translate the genetic information into proteins, leading to the production of new virus particles and the continuation of the viral life cycle. Examples of human diseases caused by RNA viruses include influenza, COVID-19 (SARS-CoV-2), hepatitis C, and polio.

There is no single medical definition for "Monkey Diseases." However, monkeys can carry and be infected with various diseases that are zoonotic, meaning they can be transmitted from animals to humans. Some examples include:

1. Simian Immunodeficiency Virus (SIV): A virus similar to Human Immunodeficiency Virus (HIV) that causes AIDS in monkeys. It is not typically harmful to monkeys but can cause AIDS in humans if transmitted, which is rare.
2. Herpes B Virus: Also known as Macacine herpesvirus 1 or Cercopithecine herpesvirus 1, it is a virus that commonly infects macaque monkeys. It can be transmitted to humans through direct contact with an infected monkey's saliva, eye fluid, or cerebrospinal fluid, causing a severe and potentially fatal illness called B encephalitis.
3. Tuberculosis (TB): Monkeys can contract and transmit tuberculosis to humans, although it is not common.
4. Simian Retrovirus (SRV): A virus that can infect both monkeys and great apes, causing immunodeficiency similar to HIV/AIDS in humans. It is not known to infect or cause disease in humans.
5. Various parasitic diseases: Monkeys can carry and transmit several parasites, including malaria-causing Plasmodium species, intestinal worms, and other parasites that can affect human health.

It's important to note that while monkeys can carry and transmit these diseases, the risk of transmission is generally low, and most cases occur in individuals who have close contact with monkeys, such as primatologists, zookeepers, or laboratory workers. Always follow safety guidelines when interacting with animals, including monkeys, to minimize the risk of disease transmission.

Viral proteins are the proteins that are encoded by the viral genome and are essential for the viral life cycle. These proteins can be structural or non-structural and play various roles in the virus's replication, infection, and assembly process. Structural proteins make up the physical structure of the virus, including the capsid (the protein shell that surrounds the viral genome) and any envelope proteins (that may be present on enveloped viruses). Non-structural proteins are involved in the replication of the viral genome and modulation of the host cell environment to favor viral replication. Overall, a thorough understanding of viral proteins is crucial for developing antiviral therapies and vaccines.

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

Viral diseases are illnesses caused by the infection and replication of viruses in host organisms. These infectious agents are obligate parasites, meaning they rely on the cells of other living organisms to survive and reproduce. Viruses can infect various types of hosts, including animals, plants, and microorganisms, causing a wide range of diseases with varying symptoms and severity.

Once a virus enters a host cell, it takes over the cell's machinery to produce new viral particles, often leading to cell damage or death. The immune system recognizes the viral components as foreign and mounts an immune response to eliminate the infection. This response can result in inflammation, fever, and other symptoms associated with viral diseases.

Examples of well-known viral diseases include:

1. Influenza (flu) - caused by influenza A, B, or C viruses
2. Common cold - usually caused by rhinoviruses or coronaviruses
3. HIV/AIDS - caused by human immunodeficiency virus (HIV)
4. Measles - caused by measles morbillivirus
5. Hepatitis B and C - caused by hepatitis B virus (HBV) and hepatitis C virus (HCV), respectively
6. Herpes simplex - caused by herpes simplex virus type 1 (HSV-1) or type 2 (HSV-2)
7. Chickenpox and shingles - both caused by varicella-zoster virus (VZV)
8. Rabies - caused by rabies lyssavirus
9. Ebola - caused by ebolaviruses
10. COVID-19 - caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Prevention and treatment strategies for viral diseases may include vaccination, antiviral medications, and supportive care to manage symptoms while the immune system fights off the infection.

Terminal repeat sequences (TRS) are repetitive DNA sequences that are located at the termini or ends of chromosomes, plasmids, and viral genomes. They play a significant role in various biological processes such as genome replication, packaging, and integration. In eukaryotic cells, telomeres are the most well-known TRS, which protect the chromosome ends from degradation, fusion, and other forms of DNA damage.

Telomeres consist of repetitive DNA sequences (5'-TTAGGG-3' in vertebrates) that are several kilobases long, associated with a set of shelterin proteins that protect them from being recognized as double-strand breaks by the DNA repair machinery. With each cell division, telomeres progressively shorten due to the end replication problem, which can ultimately lead to cellular senescence or apoptosis.

In contrast, prokaryotic TRS are often found at the ends of plasmids and phages and are involved in DNA replication, packaging, and integration into host genomes. For example, the attP and attB sites in bacteriophage lambda are TRS that facilitate site-specific recombination during integration and excision from the host genome.

Overall, terminal repeat sequences are essential for maintaining genome stability and integrity in various organisms, and their dysfunction can lead to genomic instability, disease, and aging.

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

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

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

I believe you are asking for a description or explanation of the indigenous peoples of South America, rather than a "medical definition." A medical definition would typically apply to a condition or disease. Here is some information about the indigenous peoples of South America:

The indigenous peoples of South America are the original inhabitants of the continent and its islands, who lived there before the European colonization. They include a wide variety of ethnic groups, languages, and cultures, with distinct histories and traditions. Many indigenous communities in South America have faced significant challenges, including displacement from their lands, marginalization, and discrimination.

According to estimates by the United Nations, there are approximately 45 million indigenous people in Latin America, of which about 30 million live in South America. They represent around 7% of the total population of South America. Indigenous peoples in South America can be found in all countries, with the largest populations in Bolivia (62%), Guatemala (41%), and Peru (25%).

Indigenous peoples in South America have a rich cultural heritage, including unique languages, arts, and spiritual practices. Many of these cultures are under threat due to globalization, urbanization, and the loss of traditional lands and resources. In recent years, there has been increased recognition of the rights of indigenous peoples in international law, including the right to self-determination, cultural heritage, and free, prior, and informed consent for projects that affect their territories. However, significant challenges remain, and many indigenous communities continue to face violence, discrimination, and poverty.

A Radioimmunoprecipitation Assay (RIA) is a highly sensitive laboratory technique used to measure the presence and concentration of specific antigens or antibodies in a sample. This technique combines the use of radioisotopes, immunochemistry, and precipitation reactions.

In an RIA, a known quantity of a radioactively labeled antigen (or hapten) is incubated with a sample containing an unknown amount of antibody (or vice versa). If the specific antigen-antibody pair is present in the sample, they will bind together to form an immune complex. This complex can then be selectively precipitated from the solution using a second antibody that recognizes and binds to the first antibody, thus forming an insoluble immune precipitate.

The amount of radioactivity present in the precipitate is directly proportional to the concentration of antigen or antibody in the sample. By comparing this value to a standard curve generated with known concentrations of antigen or antibody, the unknown concentration can be accurately determined. RIAs have been widely used in research and clinical settings for the quantification of various hormones, drugs, vitamins, and other biomolecules. However, due to safety concerns and regulatory restrictions associated with radioisotopes, non-radioactive alternatives like Enzyme-Linked Immunosorbent Assays (ELISAs) have become more popular in recent years.

Virus assembly, also known as virion assembly, is the final stage in the virus life cycle where individual viral components come together to form a complete viral particle or virion. This process typically involves the self-assembly of viral capsid proteins around the viral genome (DNA or RNA) and, in enveloped viruses, the acquisition of a lipid bilayer membrane containing viral glycoproteins. The specific mechanisms and regulation of virus assembly vary among different viral families, but it is often directed by interactions between viral structural proteins and genomic nucleic acid.

A plant virus is not defined in medical terms, as viruses are typically considered within the context of living organisms and plants are not classified as such. However, I can provide a general virology definition for you:

Plant viruses are small infectious agents that consist of nucleic acid (DNA or RNA) enclosed in a protein coat. They infect various plant species, causing a wide range of symptoms and diseases, which can result in significant economic losses in agriculture and horticulture. Plant viruses lack the ability to replicate outside a host cell, and they rely on the host's metabolic machinery for their reproduction. They can be transmitted through various means, such as insect vectors, seeds, or mechanical contact.

DNA viruses are a type of virus that contain DNA (deoxyribonucleic acid) as their genetic material. These viruses replicate by using the host cell's machinery to synthesize new viral components, which are then assembled into new viruses and released from the host cell.

DNA viruses can be further classified based on the structure of their genomes and the way they replicate. For example, double-stranded DNA (dsDNA) viruses have a genome made up of two strands of DNA, while single-stranded DNA (ssDNA) viruses have a genome made up of a single strand of DNA.

Examples of DNA viruses include herpes simplex virus, varicella-zoster virus, human papillomavirus, and adenoviruses. Some DNA viruses are associated with specific diseases, such as cancer (e.g., human papillomavirus) or neurological disorders (e.g., herpes simplex virus).

It's important to note that while DNA viruses contain DNA as their genetic material, RNA viruses contain RNA (ribonucleic acid) as their genetic material. Both DNA and RNA viruses can cause a wide range of diseases in humans, animals, and plants.

A Cytopathic Effect (CPE) is a visible change in the cell or group of cells due to infection by a pathogen, such as a virus. When the cytopathic effect is caused specifically by a viral infection, it is referred to as a "Viral Cytopathic Effect" (VCPE).

The VCPE can include various changes in the cell's morphology, size, and structure, such as rounding, shrinkage, multinucleation, inclusion bodies, and formation of syncytia (multinucleated giant cells). These changes are often used to identify and characterize viruses in laboratory settings.

The VCPE is typically observed under a microscope after the virus has infected cell cultures, and it can help researchers determine the type of virus, the degree of infection, and the effectiveness of antiviral treatments. The severity and timing of the VCPE can vary depending on the specific virus and the type of cells that are infected.

Defective viruses are viruses that have lost the ability to complete a full replication cycle and produce progeny virions independently. These viruses require the assistance of a helper virus, which provides the necessary functions for replication. Defective viruses can arise due to mutations, deletions, or other genetic changes that result in the loss of essential genes. They are often non-infectious and cannot cause disease on their own, but they may interfere with the replication of the helper virus and modulate the course of infection. Defective viruses can be found in various types of viruses, including retroviruses, bacteriophages, and DNA viruses.

Viral regulatory and accessory proteins are a type of viral protein that play a role in the regulation of viral replication, gene expression, and host immune response. These proteins are not directly involved in the structural components of the virus but instead help to modulate the environment inside the host cell to facilitate viral replication and evade the host's immune system.

Regulatory proteins control various stages of the viral life cycle, such as transcription, translation, and genome replication. They may also interact with host cell regulatory proteins to alter their function and promote viral replication. Accessory proteins, on the other hand, are non-essential for viral replication but can enhance viral pathogenesis or modulate the host's immune response.

The specific functions of viral regulatory and accessory proteins vary widely among different viruses. For example, in human immunodeficiency virus (HIV), the Tat protein is a regulatory protein that activates transcription of the viral genome, while the Vpu protein is an accessory protein that downregulates the expression of CD4 receptors on host cells to prevent superinfection.

Understanding the functions of viral regulatory and accessory proteins is important for developing antiviral therapies and vaccines, as these proteins can be potential targets for inhibiting viral replication or modulating the host's immune response.

"Genes x Environment" (GxE) is a term used in the field of genetics to describe the interaction between genetic factors and environmental influences on the development, expression, and phenotypic outcome of various traits, disorders, or diseases. This concept recognizes that both genes and environment play crucial roles in shaping an individual's health and characteristics, and that these factors do not act independently but rather interact with each other in complex ways.

GxE interactions can help explain why some individuals with a genetic predisposition for a particular disorder may never develop the condition, while others without such a predisposition might. The environmental factors involved in GxE interactions can include lifestyle choices (such as diet and exercise), exposure to toxins or pollutants, social experiences, and other external conditions that can influence gene expression and overall health outcomes.

Understanding GxE interactions is essential for developing personalized prevention and treatment strategies, as it allows healthcare providers to consider both genetic and environmental factors when assessing an individual's risk for various disorders or diseases.

I'm sorry for any confusion, but "Peru" is not a medical term. It is a country located in South America, known for its rich history, diverse culture, and beautiful landscapes. If you have any questions about medical terms or concepts, I would be happy to help answer those!

Repetitive sequences in nucleic acid refer to repeated stretches of DNA or RNA nucleotide bases that are present in a genome. These sequences can vary in length and can be arranged in different patterns such as direct repeats, inverted repeats, or tandem repeats. In some cases, these repetitive sequences do not code for proteins and are often found in non-coding regions of the genome. They can play a role in genetic instability, regulation of gene expression, and evolutionary processes. However, certain types of repeat expansions have been associated with various neurodegenerative disorders and other human diseases.

Sindbis virus is an alphavirus that belongs to the Togaviridae family. It's named after the location where it was first isolated, in Sindbis, Egypt, in 1952. This virus is primarily transmitted by mosquitoes and can infect a wide range of animals, including birds and humans. In humans, Sindbis virus infection often causes a mild flu-like illness characterized by fever, rash, and joint pain. However, some people may develop more severe symptoms, such as neurological disorders, although this is relatively rare. There is no specific treatment for Sindbis virus infection, and management typically involves supportive care to alleviate symptoms.

Measles virus is a single-stranded, negative-sense RNA virus belonging to the genus Morbillivirus in the family Paramyxoviridae. It is the causative agent of measles, a highly contagious infectious disease characterized by fever, cough, runny nose, and a red, blotchy rash. The virus primarily infects the respiratory tract and then spreads throughout the body via the bloodstream.

The genome of the measles virus is approximately 16 kilobases in length and encodes for eight proteins: nucleocapsid (N), phosphoprotein (P), matrix protein (M), fusion protein (F), hemagglutinin (H), large protein (L), and two non-structural proteins, V and C. The H protein is responsible for binding to the host cell receptor CD150 (SLAM) and mediating viral entry, while the F protein facilitates fusion of the viral and host cell membranes.

Measles virus is transmitted through respiratory droplets and direct contact with infected individuals. The virus can remain airborne for up to two hours in a closed space, making it highly contagious. Measles is preventable through vaccination, which has led to significant reductions in the incidence of the disease worldwide.

"Gene products, GAG" refer to the proteins that are produced by the GAG (Group-specific Antigen) gene found in retroviruses, such as HIV (Human Immunodeficiency Virus). These proteins play a crucial role in the structure and function of the viral particle or virion.

The GAG gene encodes for a polyprotein that is cleaved by a protease into several individual proteins, including matrix (MA), capsid (CA), and nucleocapsid (NC) proteins. These proteins are involved in the formation of the viral core, which encloses the viral RNA genome and associated enzymes required for replication.

The MA protein is responsible for binding to the host cell membrane during viral entry, while the CA protein forms the capsid shell that surrounds the viral RNA and NC protein. The NC protein binds to the viral RNA and helps to package it into the virion during assembly. Overall, GAG gene products are essential for the life cycle of retroviruses and are important targets for antiretroviral therapy in HIV-infected individuals.

'Influenza A Virus, H1N1 Subtype' is a specific subtype of the influenza A virus that causes flu in humans and animals. It contains certain proteins called hemagglutinin (H) and neuraminidase (N) on its surface, with this subtype specifically having H1 and N1 antigens. The H1N1 strain is well-known for causing the 2009 swine flu pandemic, which was a global outbreak of flu that resulted in significant morbidity and mortality. This subtype can also cause seasonal flu, although the severity and symptoms may vary. It is important to note that influenza viruses are constantly changing, and new strains or subtypes can emerge over time, requiring regular updates to vaccines to protect against them.

Seroepidemiologic studies are a type of epidemiological study that measures the presence and levels of antibodies in a population's blood serum to investigate the prevalence, distribution, and transmission of infectious diseases. These studies help to identify patterns of infection and immunity within a population, which can inform public health policies and interventions.

Seroepidemiologic studies typically involve collecting blood samples from a representative sample of individuals in a population and testing them for the presence of antibodies against specific pathogens. The results are then analyzed to estimate the prevalence of infection and immunity within the population, as well as any factors associated with increased or decreased risk of infection.

These studies can provide valuable insights into the spread of infectious diseases, including emerging and re-emerging infections, and help to monitor the effectiveness of vaccination programs. Additionally, seroepidemiologic studies can also be used to investigate the transmission dynamics of infectious agents, such as identifying sources of infection or tracking the spread of antibiotic resistance.

A "cell line, transformed" is a type of cell culture that has undergone a stable genetic alteration, which confers the ability to grow indefinitely in vitro, outside of the organism from which it was derived. These cells have typically been immortalized through exposure to chemical or viral carcinogens, or by introducing specific oncogenes that disrupt normal cell growth regulation pathways.

Transformed cell lines are widely used in scientific research because they offer a consistent and renewable source of biological material for experimentation. They can be used to study various aspects of cell biology, including signal transduction, gene expression, drug discovery, and toxicity testing. However, it is important to note that transformed cells may not always behave identically to their normal counterparts, and results obtained using these cells should be validated in more physiologically relevant systems when possible.

Skin diseases of viral origin are conditions that affect the skin caused by viral infections. These infections can lead to various symptoms such as rashes, blisters, papules, and skin lesions. Some common examples of viral skin diseases include:

1. Herpes Simplex Virus (HSV) infection: This causes cold sores or genital herpes, which are characterized by small, painful blisters on the skin.
2. Varicella-zoster virus (VZV) infection: This causes chickenpox and shingles, which are characterized by itchy, fluid-filled blisters on the skin.
3. Human Papillomavirus (HPV) infection: This causes warts, which are small, rough growths on the skin.
4. Molluscum contagiosum: This is a viral infection that causes small, raised, and pearly white bumps on the skin.
5. Measles: This is a highly contagious viral disease characterized by fever, cough, runny nose, and a rash that spreads all over the body.
6. Rubella: Also known as German measles, this viral infection causes a red rash on the face and neck that spreads to the rest of the body.

Viral skin diseases can be spread through direct contact with an infected person or contaminated objects, such as towels or bedding. Some viral skin diseases can be prevented through vaccination, while others can be treated with antiviral medications or other therapies.

The "env" gene in the Human Immunodeficiency Virus (HIV) encodes for the envelope proteins gp120 and gp41, which are located on the surface of the viral particle. These proteins play a crucial role in the virus's ability to infect human cells.

The gp120 protein is responsible for binding to CD4 receptors and co-receptors (CCR5 or CXCR4) on the surface of host cells, primarily CD4+ T cells, dendritic cells, and macrophages. This interaction allows the virus to attach to and enter the host cell, initiating infection.

The gp41 protein then facilitates the fusion of the viral and host cell membranes, enabling the viral genetic material to be released into the host cell's cytoplasm. Once inside the host cell, HIV can integrate its genome into the host cell's DNA, leading to the production of new virus particles and the continued spread of infection.

Understanding the function of the env gene products is essential for developing effective HIV treatments and vaccines, as targeting these proteins can prevent viral entry and subsequent infection of host cells.

Rabies is a viral disease that affects the nervous system of mammals, including humans. It's caused by the rabies virus (RV), which belongs to the family Rhabdoviridae and genus Lyssavirus. The virus has a bullet-shaped appearance under an electron microscope and is encased in a lipid envelope.

The rabies virus primarily spreads through the saliva of infected animals, usually via bites. Once inside the body, it travels along nerve fibers to the brain, where it multiplies rapidly and causes inflammation (encephalitis). The infection can lead to symptoms such as anxiety, confusion, hallucinations, seizures, paralysis, coma, and ultimately death if left untreated.

Rabies is almost always fatal once symptoms appear, but prompt post-exposure prophylaxis (PEP), which includes vaccination and sometimes rabies immunoglobulin, can prevent the disease from developing when administered after an exposure to a potentially rabid animal. Pre-exposure vaccination is also recommended for individuals at high risk of exposure, such as veterinarians and travelers visiting rabies-endemic areas.

A "gene" is a basic unit of heredity in living organisms. It is a segment of DNA (deoxyribonucleic acid) that contains the instructions for the development and function of an organism. Genes are responsible for inherited traits, such as eye color, hair color, and height, as well as susceptibility to certain diseases.

"Pol" is short for "polymerase," which is an enzyme that helps synthesize DNA or RNA (ribonucleic acid). In the context of genes, "pol" often refers to "DNA polymerase," an enzyme that plays a crucial role in DNA replication and repair.

Therefore, "genes, pol" may refer to the genes involved in the regulation or function of DNA polymerases. These genes are essential for maintaining the integrity and stability of an organism's genome. Mutations in these genes can lead to various genetic disorders and cancer.

"Influenza A Virus, H5N1 Subtype" is a specific subtype of the Influenza A virus that is often found in avian species (birds) and can occasionally infect humans. The "H5N1" refers to the specific proteins (hemagglutinin and neuraminidase) found on the surface of the virus. This subtype has caused serious infections in humans, with high mortality rates, especially in cases where people have had close contact with infected birds. It does not commonly spread from person to person, but there is concern that it could mutate and adapt to efficiently transmit between humans, which would potentially cause a pandemic.

"Dominica" is a country and not a medical term. It is an island nation located in the Caribbean Sea, known for its lush rainforests, beautiful beaches, and natural hot springs. If you are looking for medical definitions, I would be happy to help with that. Could you please provide more information or clarify your question?

Simian retroviruses are a group of retroviruses that naturally infect primates, including monkeys and apes. These viruses are closely related to human retroviruses and can cause immunodeficiency and cancer in their simian hosts. One well-known example is the Simian Immunodeficiency Virus (SIV), which is similar to Human Immunodeficiency Virus (HIV) and causes AIDS in some primate species.

Retroviruses are viruses that have an RNA genome and use a reverse transcriptase enzyme to create DNA copies of their genome, which can then be integrated into the host cell's DNA. This characteristic sets retroviruses apart from other RNA viruses. Simian retroviruses, like other retroviruses, have an envelope protein that allows them to attach to and enter host cells.

It is important to note that simian retroviruses can pose a risk to humans who come into contact with infected primates, either in captivity or in the wild. For example, SIV can be transmitted to humans through exposure to infected bodily fluids, such as blood or sexual secretions, and can cause a disease similar to AIDS known as Simian Immunodeficiency Virus Infection in Humans (SIV-infected humans). However, such transmissions are rare.

"Theropithecus" is a genus of Old World monkeys that includes the extinct species "Theropithecus oswaldi" and the currently existing species "Theropithecus gelada." These monkeys are native to Africa and are known for their distinctive long, pointed canines in males. The term "Theropithecus" comes from the Greek words "ther," meaning beast, and "pithekos," meaning ape.

It is important to note that "Theropithecus" species are not to be confused with "Theropoda," which is a group of dinosaurs that includes modern birds and their extinct relatives. The similarity in the names is purely coincidental.

Human T-cell lymphotropic virus type 1 or human T-lymphotropic virus (HTLV-I), also called the adult T-cell lymphoma virus type ... 2005). "Differences in viral and host genetic risk factors for development of human T-cell lymphotropic virus type 1 (HTLV-1)- ... Verdonck, K, González, E, Dooren, SV, Vandamme, AM, Vanham, G, Gotuzzo, E (2007). "Human T-lymphotropic virus 1: recent ... Wikimedia Commons has media related to Human T-lymphotropic virus 1. International Retrovirology Association Human+T- ...
"Human T-lymphotropic virus type 1". www.who.int. Retrieved 11 November 2021. Paiva AM, Assone T, Haziot ME, Smid J, Fonseca LA ... September 2014). "Mother-to-Child Transmission of Human T-Cell Lymphotropic Viruses-1/2: What We Know, and What Are the Gaps in ... Eusebio-Ponce E, Candel FJ, Anguita E (August 2019). "Human T-Cell Lymphotropic Virus Type 1 and associated diseases in Latin ... Boostani R, Sadeghi R, Sabouri A, Ghabeli-Juibary A (October 2018). "Human T-lymphotropic virus type I and breastfeeding; ...
Human T-lymphotropic virus 1 and HIV. Hypereosiophilia or eosinophilia may be associated with the following autoimmune diseases ... Human immunodeficiency virus infection Interstitial nephropathy Hyperimmunoglobulin E syndrome, an immune disorder ... Eosinophil counts in human blood normally range between 100 and 500 per/μL. Maintenance of these levels results from a balance ... Beeken WL, Northwood I, Beliveau C, Baigent G, Gump D (1987). "Eosinophils of human colonic mucosa: C3b and Fc gamma receptor ...
"Human T-lymphotropic virus 2". NCBI Taxonomy Browser. 11909. International Retrovirology Association Human+T-lymphotropic+virus ... A virus closely related to HTLV-I, human T-lymphotropic virus 2 (HTLV-II) shares approximately 70% genomic homology (structural ... The family of Human T-lymphotropic virus (Figure 2) can be further categorized into four sub types. The figure also divides the ... "Human T-Cell Lymphotropic Viruses (HTLV)". Medscape. Retrieved 22 February 2019. "HTLV Type I and Type II". NORD (National ...
Viruses have also been linked to some forms of leukemia. For example, human T-lymphotropic virus (HTLV-1) causes adult T-cell ... Adult T-cell leukemia is caused by human T-lymphotropic virus (HTLV), a virus similar to HIV. Like HIV, HTLV infects CD4+ T- ... Human T-cell lymphotropic virus types I and II (HTLV-I/II) are endemic in certain areas of the world.[citation needed] Clonal ... 12 (1): 17. doi:10.1186/s13045-019-0705-x. PMC 6376657. PMID 30764841. Zheng PP, Kros JM, Li J (June 2018). "Approved CAR T ...
Many viruses including herpes simplex virus (HSV), human immunodeficiency virus (HIV) and human T-lymphotropic virus (HTLV) ... "Human T-lymphotropic virus, type 1, tax protein triggers microtubule reorientation in the virological synapse". J. Biol. Chem. ... As viral synapses allow the virus to spread directly from cell to cell, they also provide a means by which the virus can escape ... "Human immunodeficiency virus type 1 envelope gp120 induces a stop signal and virological synapse formation in noninfected CD4+ ...
AIDS-related encephalomyelitis, caused by opportunistic Human T-lymphotropic virus type III (HTLV-III) infection. Chronic ... a group of viral illnesses that can affect horses and humans; collectively termed Equine encephalitis. Experimental autoimmune ... 2015 Mar 8;12(1):46. Melania Spadaro et al. Histopathology and clinical course of MOG-antibody-associated encephalomyelitis. ...
Human T-lymphotropic virus 2 (HTLV-2) has been isolated in a small number of patients with the variant form of HCL. In the ... Roucoux DF, Murphy EL (2004). "The epidemiology and disease outcomes of human T-lymphotropic virus type II". AIDS Rev. 6 (3): ... Feuer G, Green PL (September 2005). "Comparative biology of human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2". ... "Integrated human T-cell leukemia virus II genome in CD8 + T cells from a patient with "atypical" hairy cell leukemia: evidence ...
Since 1987 Bangham has conducted research on the Human T-lymphotropic virus 1 (HTLV-1). His contributions include the discovery ... "Human immunodeficiency virus genetic variation that can escape cytotoxic T cell recognition". Nature. 354 (6353): 453-459. ... subscription required) Bangham, Charles R. M. (1987). The cellular immune response to respiratory syncytial virus in mouse and ... HIV and murine leukaemia virus (MLV) are transmitted from cell-to-cell, starting a new field in virology. Bangham was elected a ...
... caused by varicella zoster virus) Chlamydia HIV Human T-lymphotropic virus Syphilis Zika fever, caused by Zika virus, can cause ... 2002). "Virus Markers Associated with Vertical Transmission of Human T Lymphotropic Virus Type 1 in Jamaica". Clinical ... June 1992). "Vertical transmission of human immunodeficiency virus (HIV) infection. Reactivity of maternal sera with ... "Maternal syphilis and vertical perinatal transmission of human immunodeficiency virus type-1 infection". International Journal ...
Examples include galactosemia, untreated HIV, untreated active tuberculosis, Human T-lymphotropic virus 1 or II, uses illicit ... "Blocking vertical transmission of human T cell lymphotropic virus type 1 and 2 through breastfeeding interruption". The ... Most Important - Galactosemia An individual with T cell lymphotropic virus type 1 and 2 will have excessive amounts of T-cell ... If a mother contains this virus and is not aware of it the spread to her infant can be at an all time high of 25%. There is ...
This includes Human T-lymphotrophic viruses (HTLVs), bovine leukaemia virus (BLV) and simian T-lymphotropic viruses (STLVs). ... "The tax gene of human T-cell leukemia virus type 2 is essential for transformation of human T lymphocytes". Journal of Virology ... Tax is produced by members of the retroviral family primate T-lymphotropic virus, which are classified as Deltaretroviruses. ... "Human T Cell Leukemia Virus Type 1 Tax Inhibits Innate Antiviral Signaling via NF-κB-Dependent Induction of SOCS1". Journal of ...
Voevodin, A; Gessain, A (1997). "Common origin of human T-lymphotropic virus type-I from Iran, Kuwait, Israel, and La Réunion ... an encyclopedia of monkey and ape viruses and non-human primate models of human viral diseases. All-USSR Prize for Young ... His research focused on the oncogenic viruses, mostly of non-human primates. In 1984 he defended his D.Sc. dissertation " ... "Antibodies reacting with human T-lymphotropic retrovirus (HTLV-I) or related antigens in lymphomatous and healthy hamadryas ...
Sawaya BE, Khalili K, Amini S (1998). "Transcription of the human immunodeficiency virus type 1 (HIV-1) promoter in central ... 1989). "Two human genes isolated by a novel method encode DNA-binding proteins containing a common region of homology". Gene. ... YBX1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) This article incorporates text ... Horwitz EM, Maloney KA, Ley TJ (1994). "A human protein containing a "cold shock" domain binds specifically to H-DNA upstream ...
A human T-lymphotropic virus antibody test, developed by Mucke's team but never marketed, served to demonstrate the first ... High proviral load of human T-lymphotropic virus type I in patients with myelodysplastic syndrome carrying HLA-A26. Leuk ... He developed an indirect immunofluorescence assay for the detection of antibodies to the human immunodeficiency virus in human ... Association of human T-cell leukemia virus and myelodysplastic syndrome in a central European population. Cancer Res. 57(21), ...
It can enhance the activity of proteins for viruses that cause cancer such as human T-cell lymphotropic virus type-1 (HTLV), ... "A human T-cell lymphotropic virus type 1 enhancer of Myc transforming potential stabilizes Myc-TIP60 transcriptional ... Additionally, KAT5 reacts with human papillomavirus (HPV), the virus responsible for cervical cancer. Other proteins that KAT5 ... Van Den Broeck A, Nissou D, Brambilla E, Eymin B, Gazzeri S (Feb 2012). "Activation of a Tip60/E2F1/ERCC1 network in human lung ...
Human T-Cell Lymphotropic Viruses~treatment at eMedicine Prayson, Richard A. (2011-11-15). Neuropathology. Elsevier Health ... Blood transfusion products are screened for human T-lymphotropic virus 1 (HTLV-1) antibodies, as a preventive measure. Some of ... Centers for Disease Control (CDC) (1988). "Licensure of screening tests for antibody to human T-lymphotropic virus type I". ... Nagamine, Yuito; Hayashi, Takeshi; Kato, Yuji; Horiuchi, Yohsuke; Tanahashi, Norio (2015). "Human T Lymphotropic Virus Type-1- ...
Bushmeat hunters in Central Africa infected with the human T-lymphotropic virus were closely exposed to wild primates. Results ... "Emergence of unique primate T-lymphotropic viruses among central African bushmeat hunters". Proceedings of the National Academy ... Shooting an animal in a confined area (canned hunting). Stephen Corry, the director of the human rights group Survival ... Emergence of zoonotic diseases caused by transmission of highly variable retrovirus chains: Outbreaks of the Ebola virus in the ...
... human T-lymphotropic virus types I and II compared with human immunodeficiency virus type 1". Transfusion. 34 (6): 478-83. doi: ... Criminal transmission of HIV is the intentional or reckless infection of a person with the human immunodeficiency virus (HIV). ... Benaissa has claimed she had been told by doctors that the risk of passing on the virus was "practically zero". The HIV trial ... E.J. Bernard (22 July 2010). "Where HIV is a crime, not just a virus: a global ranking of prosecutions for HIV non-disclosure, ...
1983: Mitsuaki Yoshida identified the molecular structure of human T-lymphotropic virus 1 responsible for adult T-cell leukemia ...
hnRNP A1's anti-viral effect is present in human T-cell lymphotropic virus type I (HTLV-1) cell culture model. hnRNP A1 ... As a result, the role of hnRNPA1 in HIV-1's life cycle is somewhat controversial. Mutations in hnRNP A1 are a cause of ... In the case of some viruses, such as human immunodeficiency virus 1 (HIV-1), contradictory results have been reported in ... In the case of Hepatitis C virus (HCV), a positive sense RNA virus, hnRNP A1 interacts with a crucial region near the 3' end of ...
"Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-1 tax and cAMP-responsive element ... CREM+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Human CREM genome location and ... cAMP responsive element modulator is a protein that in humans is encoded by the CREM gene, and it belongs to the cAMP- ... Less IL-2 will be produced from T cells in humans or mice with systemic lupus erythematousus (SLE). Some studies showed that an ...
Mariner JM, Lantz V, Waldmann TA, Azimi N (2001). "Human T cell lymphotropic virus type I Tax activates IL-15R alpha gene ... Mortier E, Bernard J, Plet A, Jacques Y (2004). "Natural, proteolytic release of a soluble form of human IL-15 receptor alpha- ... Interleukin 15 receptor, alpha subunit is a subunit of the interleukin 15 receptor that in humans is encoded by the IL15RA gene ... Jacob CO, Mykytyn K, Varcony T, Drabkin HA (1993). "Mapping of the interleukin 5 receptor gene to human chromosome 3 p25-p26 ...
... studied adult T-cell leukemia that develops in individuals infected with the retrovirus human T-cell lymphotropic virus-1 (HTLV ... "Therapy of patients with human T-cell lymphotrophic virus I-induced adult T-cell leukemia with anti-Tac, a monoclonal antibody ... "Vaccinia virus-based multivalent H5N1 avian influenza vaccines adjuvanted with IL-15 confer sterile cross-clade protection in ... "A monoclonal antibody (anti-Tac) reactive with activated and functionally mature human T cells. I. Production of anti-Tac ...
In central Australia, Indigenous Australians have human T-lymphotropic virus 1 at a rate thousands of times higher than non- ... Allam, Lorena (24 April 2018). "'People are scared': the fight against a deadly virus no one has heard of". The Guardian. ... This prompted health and human rights activists to establish the "Close the Gap" campaign, which focused on health equality for ... "Close the Gap report - "Our Choices, Our Voices" (2019)". Australian Human Rights Commission. Retrieved 15 January 2020. Bond, ...
II carboxyl-terminal domain for activated transcription of human retroviruses human T-cell lymphotropic virus I and HIV-1". J. ... 1996). "The human immunodeficiency virus type 1 Vpr transactivator: cooperation with promoter-bound activator domains and ... Wu-Baer F, Sigman D, Gaynor RB (1995). "Specific binding of RNA polymerase II to the human immunodeficiency virus trans- ... Keen NJ, Gait MJ, Karn J (1996). "Human immunodeficiency virus type-1 Tat is an integral component of the activated ...
II carboxyl-terminal domain for activated transcription of human retroviruses human T-cell lymphotropic virus I and HIV-1". J. ... 1996). "The human immunodeficiency virus type 1 Vpr transactivator: cooperation with promoter-bound activator domains and ... Wu-Baer F, Sigman D, Gaynor RB (1995). "Specific binding of RNA polymerase II to the human immunodeficiency virus trans- ... Keen NJ, Gait MJ, Karn J (1996). "Human immunodeficiency virus type-1 Tat is an integral component of the activated ...
II carboxyl-terminal domain for activated transcription of human retroviruses human T-cell lymphotropic virus I and HIV-1". J. ... 1996). "The human immunodeficiency virus type 1 Vpr transactivator: cooperation with promoter-bound activator domains and ... Wu-Baer F, Sigman D, Gaynor RB (1995). "Specific binding of RNA polymerase II to the human immunodeficiency virus trans- ... Keen NJ, Gait MJ, Karn J (1996). "Human immunodeficiency virus type-1 Tat is an integral component of the activated ...
II carboxyl-terminal domain for activated transcription of human retroviruses human T-cell lymphotropic virus I and HIV-1". J. ... Agostini I, Navarro JM, Rey F, Bouhamdan M, Spire B, Vigne R, Sire J (1996). "The human immunodeficiency virus type 1 Vpr ... Wu-Baer F, Sigman D, Gaynor RB (1995). "Specific binding of RNA polymerase II to the human immunodeficiency virus trans- ... Keen NJ, Gait MJ, Karn J (1996). "Human immunodeficiency virus type-1 Tat is an integral component of the activated ...
II carboxyl-terminal domain for activated transcription of human retroviruses human T-cell lymphotropic virus I and HIV-1". J. ... Jang KL, Collins MK, Latchman DS (1992). "The human immunodeficiency virus tat protein increases the transcription of human Alu ... Agostini I, Navarro JM, Rey F, Bouhamdan M, Spire B, Vigne R, Sire J (1996). "The human immunodeficiency virus type 1 Vpr ... Wu-Baer F, Sigman D, Gaynor RB (1995). "Specific binding of RNA polymerase II to the human immunodeficiency virus trans- ...
Human T-cell lymphotropic virus type 1 or human T-lymphotropic virus (HTLV-I), also called the adult T-cell lymphoma virus type ... 2005). "Differences in viral and host genetic risk factors for development of human T-cell lymphotropic virus type 1 (HTLV-1)- ... Verdonck, K, González, E, Dooren, SV, Vandamme, AM, Vanham, G, Gotuzzo, E (2007). "Human T-lymphotropic virus 1: recent ... Wikimedia Commons has media related to Human T-lymphotropic virus 1. International Retrovirology Association Human+T- ...
A cross-sectional study enrolling HTLV-1-infected individuals with chronic joint pain aged up to 75 years, both sexes, and ... Joint pain in Individuals Infected with Human T-lymphotropic Virus Type 1 (HTLV-1) on Radiographs. Sep 13, 2022 ... Increased proinflammatory cytokines were seen in the patients when the virus infects their CD4+ and CD8+ positive cells, ... The purpose of this study was to describe the clinical and radiological features of her HTLV-1-infected patient with joint pain ...
The Human T-lymphotropic virus type 1 (HTLV-1) is a human retrovirus that is known to cause a type of cancer; referred to as ... Detection test kit of Human T-lymphoptropic virus type 1 by using qPCR. ... The Human T-lymphotropic virus type 1 (HTLV-1) is a human retrovirus that is known to cause a type of cancer; referred to as ... Real Time PCR Detection Kit Human T-lymphotropic virus type 1. Item code. GPCRsHTLV1 ...
Human T-Lymphotropic Virus Type 1 (Htlv-1): a new subgroup within the cosmopolitan subtype. *María Eirin1, ... Eirin, M., Jones, L., Berini, C. et al. Human T-Lymphotropic Virus Type 1 (Htlv-1): a new subgroup within the cosmopolitan ... Human T-Lymphotropic Virus Type 1 (Htlv-1): a new subgroup within the cosmopolitan subtype ... HTLV-1 is classified in seven subtypes (a-g) most of them restricted to specific regions (b-e), while the Cosmopolitan subtype ...
Diversity of Human T-Lymphotropic Virus type 1 Cosmopolitan subtype (HTLV-1a) circulating in infected-residents in Portugal. by ... Physiotherapy Methods Applied in the Prevention of Functional Loss Associated with Human T-Lymphotropic Virus 1 Infection: An ... especially the study of human T-lymphotropic virus (HTLV) infections and the associated diseases, to foster collaborations ... Detection of early phase human T-cell leukemia virus type 1 and 2 infection with an improved confirmatory test. September 26, ...
Classification system for human T-lymphotropic virus type III/lymphadenopathy-associated virus infections. MMWR 1986;35:334- ... Primary human T-lymphotropic virus type III infection. Ann Intern Med 1985;103:880-3. ... Impact of the human immunodeficiency virus epidemic on mortality trends in young men, United States. Am J Public Health 1990;80 ... Impact of the human immunodeficiency virus epidemic on mortality in women of reproductive age, United States. JAMA 1990;264:225 ...
Human T-cell lymphotropic virus type-1 (HTLV-1) may cause severe diseases such as HTLV-1-associated myelopathy/tropical spastic ... Early Juvenile Human T-cell Lymphotropic Virus Type-1-Associated Myelopathy/Tropical Spastic Paraparesis: Study of 25 Patients. ... The patients were HTLV-1+ and were submitted to dermatological and neurological examinations. Diagnosis of HAM/TSP was ... Progressão da Doença Infecções por HTLV-I/complicações Vírus Linfotrópico T Tipo 1 Humano/isolamento & purificação Transmissão ...
Human T-cell lymphotropic virus types I and II infections in mother-child pairs in Nigeria. J Trop Pediatr 1999;45:66-70.. ... Seroepidemiology of human T-cell lymphotropic virus type I/II in Benin (West Africa). AIDS Res Hum Retrovirus 1991;7:447-51.. ... Human T-cell lymphotropic virus (HTLV) and its subtypes were estimated to have infected 5-10 million people worldwide [1-3]. ... Prevalence of human T-lymphotropic virus type 1 and 2 (HTLV-1/-2) infection in pregnant women in Brazil: a systematic review ...
Human T cell lymphotropic virus type II and human immunodeficiency virus type 1 disease progression (multiple letters). In: ... Human T cell lymphotropic virus type II and human immunodeficiency virus type 1 disease progression (multiple letters). / ... Human T cell lymphotropic virus type II and human immunodeficiency virus type 1 disease progression (multiple letters). ... T1 - Human T cell lymphotropic virus type II and human immunodeficiency virus type 1 disease progression (multiple letters) ...
N2 - Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be reported and is associated with ... AB - Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be reported and is associated with ... Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be reported and is associated with neoplastic ... abstract = "Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be reported and is associated ...
... while in human T-lymphotropic virus type 1 (HTVL-1) positive B cell lines, only THC increased IL-8 levels [106]. Cutando and co ... human T-lymphotropic virus type 1; PFC: prefrontal cortex; PMBC: peripheral mononuclear cells; mPFC: medial prefrontal cortex; ... human serum. in patients with depression. [152]. KYN ↑. female human serum. in early puerperium associated with anxiety and ... human plasma. in patients with unipolar treatment-resistant depression. [154]. KYN and QUIN ↑. human plasma. did not mediate ...
The most common and clinically important pathogenic species in humans is S stercoralis (see the following image). ... Human T-cell lymphotropic virus-I in Latin America. Infect Dis Clin North Am. 2000 Mar. 14 (1):211-39, x-xi. [QxMD MEDLINE Link ... Human T-cell leukemia virus type 1 (HTLV-1) infection [9, 10] : HTLV-1, the retrovirus associated with adult T-cell leukemia, ... Atypical clinical presentation of strongyloidiasis in a patient co-infected with human T cell lymphotrophic virus type I. Am J ...
Classification system for human T-lymphotropic virus type III/lymphadenopathy-associated virus infections. MMWR 1986;35:334-9. ... Primary human T-lymphotropic virus type III infection. Ann Intern Med 1985;103:880-3. * Tindall B, Cooper DA. Primary HIV ... Impact of the human immunodeficiency virus epidemic on mortality trends in young men, United States. Am J Public Health 1990;80 ... Prognosis of human immunodeficiency virus in children and adolescents. Pediatr Infect Dis J 1989;8:216-20. * Goedert JJ, Biggar ...
Human T cell leukemia virus transformation of cells ... Human T-lymphotropic virus 1--pathogenicity. Leukemia-Lymphoma ... Human T-cell Leukemia Virus type 1 (HTLV-1) is a delta-retrovirus that infects approximately 20 million individuals worldwide. ... CIT): Human T-cell Leukemia Virus type 1 (HTLV-1) is a delta-retrovirus that infects approximately 20 million individuals ... Nuclear damage and miscounted chromosomes: Human T cell leukemia virus transformation of cells. Download VideoCast. You can ...
Kaposi sarcoma (human herpesvirus 8). *Adult T-cell leukemia/lymphoma (human T-lymphotropic virus-1) ... National Library of Medicine 8600 Rockville Pike, Bethesda, MD 20894 U.S. Department of Health and Human Services National ... Some liver cancers (hepatitis B and hepatitis C viruses). * ... Burkitt lymphoma (Epstein-Barr virus). *Cervical cancer (human ... Types of tumors known to be caused by or linked with viruses are:. * ...
A Fully Annotated Genome Sequence of Human T-Cell Lymphotropic Virus Type 1 (HTLV-1)  Barreto, Fernanda Khouri et al. , Date ...
Human T-lymphotropic virus type I/II (HTLV-I/II); Human immunodeficiency virus (HIV) p24 antigen; Human immunodeficiency virus ... Human T-lymphotropic virus type I/II (HTLV-I/II); Human immunodeficiency virus (HIV) p24 antigen; Human immunodeficiency virus ... Human T-lymphotropic virus type I/II (HTLV-I/II) Plasma; Serum Hepatitis B virus surface antigen (HBs Ag); Hepatitis B virus ... Human immunodeficiency virus type 2 (HIV-2) RNA Plasma Hepatitis B virus (HBV) DNA; Hepatitis C virus (HCV) viral RNA; Human ...
Safety of therapeutic immune globulin preparations with respect to transmission of human T-lymphotropic (sic) virus type III/ ... Lack of Transmission of Human Immunodeficiency Virus Through Rho(D) Immune Globulin (Human) On September 18, 1987, the Armed ... Inactivation and partition of human T-cell lymphotrophic virus, type III, during ethanol fractionation of plasma. Transfusion ... Use of trade names is for identification only and does not imply endorsement by the U.S. Department of Health and Human ...
Human T-cell lymphotropic virus type 1 (HTLV-1) infection in a cohort followed up... ... Human T-cell lymphotropic virus type 1 (HTLV-1) infection in a cohort followed up... ... Human T lymphotropic virus type 1 (HTLV-1) DNA proviral load quantification and immunological... ... Molecular diversity of the envelope and proviral load cell lymphotropic virus human... ...
Human T-cell lymphotropic virus, type I (HTLV-I) is associated to a neoplastic disorder (Adult T-cell Leukemia and Lymphoma- ... Identification of human T-cell lymphotropic virus type IIa infection in the Kayapo, an indigenous population of Brazil. AIDS ... 6. Gessain A, Vernant JC, Maurs L, Barin F, Gout O, Calender A. Antibodies to Human T-Lymphotropic Virus Type I in patients ... The epidemiology of myelopathy associated with human T-lymphotropic virus 1. Transactions of the Royal Society of Tropical ...
Human T-cell lymphotropic virus sort 1 or sort 2. *Ebola. *Herpetic lesions on the breast ... In case your child is identified with galactosemia, breastfeeding turns into unsafe in your child.1,2,3,4 Galactosemia is a ... Suppliers can reference remedy security with breastfeeding by researching the LactMed database on-line.1,2,3 ... 1,2,3 These recognized illnesses are of concern due to the potential of passing the an infection by way of breast milk or by ...
Human T lymphotropic virus type II (HTLV-II): epidemiology, molecular propeties and clinical features of infection. J Acq Imm ... Coinfection with human T-cell lymphotropic virus type I and HIV in Brazil: Impact on markers of HIV diseases progression. JAMA ... distributed pathogen and the occurrence of coinfections with other human retroviruses like the human T-cell lymphotropic virus ... Identification of T cell lymphotropic virus type IIa in the Kayapo, an indigenous population of Brazil. AIDS Res Hum Retrov 11 ...
Infection of human T lymphotropic virus type 1 (HTLV-1) and type 2 (HTL V-2) in individuals... ...
Human T-cell lymphotropic virus type 1 (HTLV-1)-associated bronchioloalveolar disorder required differentiation from fibrotic ... 18A, 18B), or exposure to low-molecular-weight chemicals [1, 3] (Fig. 7A, 7B, 7C). The histopathologic and radiologic features ... Although this classification is helpful, patients often present with both subacute and chronic findings [1, 3]. Acute HP is ... February 1, 2015 , Canadian Association of Radiologists Journal, Vol. 66, No. 1 ...
Neurological morbidity among human T-lymphotropic-virus-type-1-infected individuals in a rural West African population (31 ... 1 October, 2008) M L Stromillo, M T Dotti, M Battaglini, M Mortilla, S Bianchi, K Plewnia, L Pantoni, D Inzitari, A Federico, N ... Changing ischaemic lesion patterns in adult moyamoya disease (1 May, 2008) J-M Kim, S-H Lee, J-K Roh ...
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Purchase your Anti-HTLV Type I gp46 Clone 68/4.11.21 (1 mg) Online Today! ... 1 mg) online at ZeptoMetrix. Browse our collection of Anti-HTLV products. ... This murine monoclonal antibody reacts with Human T-Lymphotropic Virus Type I (HTLV-I) surface protein, gp46. The antibody was ... Determine the presence of Human T-Lymphotropic Virus (HTLV) Type I protein. ...
N2 - To determine the incidence of and risk factors for human T-lymphotropic virus, type II (HTLV-II) seroconversion among ... AB - To determine the incidence of and risk factors for human T-lymphotropic virus, type II (HTLV-II) seroconversion among ... To determine the incidence of and risk factors for human T-lymphotropic virus, type II (HTLV-II) seroconversion among injecting ... Dive into the research topics of Incidence and risk factors for human T-lymphotropic virus type II seroconversion among ...
  • Human T-cell lymphotropic virus type 1 or human T-lymphotropic virus (HTLV-I), also called the adult T-cell lymphoma virus type 1, is a retrovirus of the human T-lymphotropic virus (HTLV) family that has been implicated in several kinds of diseases including very aggressive adult T-cell lymphoma (ATL), HTLV-I-associated myelopathy, uveitis, Strongyloides stercoralis hyper-infection and some other diseases. (wikipedia.org)
  • It is thought that about 1-5% of infected persons develop cancer as a result of the infection with HTLV-I over their lifetimes. (wikipedia.org)
  • The infection rate is about 1% in Papua New Guinea, the Solomon Islands, and Vanuatu, where the genotype C predominates. (wikipedia.org)
  • Human T-lymphotropic virus 1 (HTLV-1) has infected human beings for thousands of years, but knowledge about the infection and its pathogenesis is only recently emerging. (nih.gov)
  • On the other hand, human T-cell lymphotropic virus type 1 seems to be a significant cofactor, with a potentially important role in HIV-1 infection. (medscape.com)
  • Although the clinical evidence is still controversial with regard to the real impact that coinfection exerts on clinical evolution, the majority of studies suggest it is associated with a modification of the natural history of HIV-1 infection, with a faster clinical progression and a shorter survival time. (medscape.com)
  • The main focus of this review is the interaction of HIV-1 and HTLV-1/2 and its clinical consequences on the natural history of HIV-1 infection. (medscape.com)
  • 2 ), we identified self-flagellation as a possible unique risk factor for HTLV-1 infection. (cdc.gov)
  • We look forward to further research that may clarify the apparent link between self-flagellation and HTLV-1 infection. (cdc.gov)
  • Trépo C , Chan HL , Lok A . Hepatitis B virus infection. (cdc.gov)
  • Gessain A , Cassar O . Epidemiological aspects and world distribution of HTLV-1 infection. (cdc.gov)
  • According to WHO , the scarcity of cost - effectiveness studies is considered one of the major barriers to the implementation of policies to prevent HTLV-1 infection . (bvsalud.org)
  • The secular trend in declining prevalence persisted after adjustment for age, time in sex work, place of birth, and HIV serostatus, with the odds of HTLV-1 infection decreasing approximately 16% per year (adjusted odds ratio = 0.84, 95% confidence interval = 0.78, 0.90). (edu.pe)
  • HTLV-1 is associated with increased susceptibility to Mycobacterium tuberculosis infection but up to now it is unknown if HTLV-1 influences the severity of tuberculosis and if tuberculosis may influence the outcome of HTLV-1. (biomedcentral.com)
  • The aims of this study were to determine the prevalence and severity of tuberculosis (TB) in HTLV-1 infected patients and analyze whether TB influences the outcome of HTLV-1 infection. (biomedcentral.com)
  • This study shows that the prevalence of M.tuberculosis infection is 6 fold higher in HTLV-1 infected individuals than that described in the Brazilian population the majority of co-infected had latent tuberculosis and HTLV-1 may influence progression from infection to HAM/TSP. (biomedcentral.com)
  • These findings have important implications in defining the epidemiological patterns of HTLV-1 infection in Nigeria. (e-cep.org)
  • The peripartum period is an important transmission time for human T-cell lymphotropic virus-1 (HTLV-1) infection, mainly via breastfeeding and partly through the placental tissues of carrier mothers. (e-cep.org)
  • Although HTLV belongs to the primate Retroviridae Family and subfamily of Oncovirinae, unlike other retroviruses, HTLV-1 subtype infection has a latency period of about 20 years. (e-cep.org)
  • DoH Digital Library: Human T-Lymphotropic Virus type 1 infection in an Indigenous Australian population: epidemiological insights from a hospital-based cohort study. (nt.gov.au)
  • Human T-Lymphotropic Virus type 1 infection in an Indigenous Australian population: epidemiological insights from a hospital-based cohort study. (nt.gov.au)
  • The Human T Lymphotropic Virus type 1 (HTLV-1) subtype C is endemic to central Australia where each of the major sequelae of HTLV-1 infection has been documented in the socially disadvantaged Indigenous population. (nt.gov.au)
  • Identifying risk factors for HTLV-1 infection is essential to direct strategies that could control HTLV-1 transmission. (nt.gov.au)
  • Risk factors for HTLV-1 infection were retrospectively determined for a cohort of Indigenous Australians who were tested for HTLV-1 at Alice Springs Hospital (ASH), 1st January 2000 to 30th June 2013. (nt.gov.au)
  • 95 % CI, 1.04-1.95) were associated with HTLV-1 infection. (nt.gov.au)
  • Although childhood infection was documented, HTLV-1 infection in adults was closely associated with increasing age, male gender and STI history. (nt.gov.au)
  • Multiple modes of transmission are therefore likely to contribute to high rates of HTLV-1 infection in the Indigenous Australian population. (nt.gov.au)
  • Human infection is acquired by penetration of the skin or mucous membranes by infective filariform larvae, either from autoinfection or from contact with infected soil or other material contaminated with human feces (fecal-oral route) (see the image below). (medscape.com)
  • The CD4+ T-lymphocyte is the primary target for HIV infection because of the affinity of the virus for the CD4 surface marker (3). (cdc.gov)
  • 18. Human T lymphotropic virus-1 infection. (nih.gov)
  • Interpretation of low level reactivity for HTLV-1/2 infection using the Abbott Architect Transfus Med. (imperial.ac.uk)
  • Switching and loss of cellular cytokine secretory capacity characterize in vivo viral infection and malignant transformation in human T- lymphotropic virus type 1 infection. (imperial.ac.uk)
  • HTLV-1 infection and Transplantation. (imperial.ac.uk)
  • In addition, I investigated the pathogenesis of myelopathy/tropical spastic paraparesis associated with human T-lymphotropic virus type-1 (HTLV-1) infection. (nih.gov)
  • HTLV tests are used for the detection of HTLV-1 and/or HTLV-II, retroviruses associated with, or suspected of causing aggressive adult T-cell lymphoma (ATL), HTLV-I-associated myelopathy, uveitis, Strongyloides stercoralis hyper-infection, neurological problems, chronic lung infections and some other diseases. (medicaldevice-network.com)
  • Epidemiological studies in humans and experimental studies in animal have shown that viral infections can induce or protect from autoimmunopathologies depending on several factors including genetic background, host-elicited immune responses, type of virus strain, viral load, and the onset time of infection. (mdpi.com)
  • ABSTRACT To evaluate the sensitivity and specificity of assays used to screen blood for antibody to hepatitis C virus (HCV) infection, the International Consortium for Blood Safety (ICBS) established fully characterized ICBS panels. (who.int)
  • Infection with hepatitis C virus (HCV) is a global health problem, with an estimated 170 million chronically infected persons worldwide. (who.int)
  • Persons with persistent HCV infection are at high risk for development of chronic liver disease, cirrhosis and hepatocellular carcinoma [1,2]. (who.int)
  • Residual risk of transfusiontransmitted infection with human immunodeficiency virus, hepatitis C virus, and hepatitis B virus in Korea from 2000 through 2010. (medigraphic.com)
  • A strength of this prospective cohort study is that it followed street youth, a marginalised and difficult-to-reach population with a high prevalence of injection drug use and blood-borne infection, including HIV and hepatitis C virus (HCV). (bmj.com)
  • The retrovirus is now generally called HTLV-I because later studies proved that ATLV is the same as the firstly identified human retrovirus called HTLV discovered by Bernard Poiesz and Francis Ruscetti and their co-workers in the laboratory of Robert C. Gallo at the National Cancer Institute. (wikipedia.org)
  • HTLV-1 is a retrovirus belonging to the family retroviridae and the genus deltaretrovirus. (wikipedia.org)
  • Human T-cell lymphotropic virus type 1 (HTLV-1) is a human retrovirus that is conclusively associated with adult T-cell leukemia and with a slowly progressive neurologic disorder, HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). (medscape.com)
  • [ 14 ] The second human retrovirus described was HTLV-2, which was isolated by Kalyanaraman, et al. (medscape.com)
  • Background Human T-cell lymphotropic virus type 1 ( HTLV-1 ) is a retrovirus that causes severe diseases , such as aggressive cancer or progressive neurological disease . (bvsalud.org)
  • Human T-cell lymphotropic virus type 1 (HTLV-1) was the first human retrovirus to be reported and is associated with neoplastic, neurological, autoimmune, and infectious complications. (edu.pe)
  • REVISED HIV CLASSIFICATION SYSTEM FOR ADOLESCENTS AND ADULTS The etiologic agent of acquired immunodeficiency syndrome (AIDS) is a retrovirus designated human immunodeficiency virus (HIV). (cdc.gov)
  • HIV-2, another human T-lymphotropic retrovirus, has been isolated in West African individuals and is closely related to simian immunodeficiency virus. (aao.org)
  • Human endogenous retrovirus type W envelope expression in blood and brain cells provides new insights into multiple sclerosis disease. (scienceblogs.com)
  • The Human T-Cell Lymphotropic Virus (HTLV) was the first human retrovirus identified and associated to leukemia/lymphoma, adult T-cells (ATL). (fiocruz.br)
  • Antiretroviral therapy promotes an inflammatory-like pattern of human T-cell lymphotropic virus type 1 (HTLV-1) replication in human immunodeficiency virus type 1/HTLV-1 co-infected individuals. (ens-lyon.fr)
  • Home / Teams / Regulation of Genome Architecture and Dynamics of Splicing (ReGArDS) - D. Auboeuf and C. Bourgeois / Publications / Antiretroviral therapy promotes an inflammatory-like pattern of human T-cell lymphotropic virus type 1 (HTLV-1) replication in human immunodeficiency virus type 1/HTLV-1 co-infected individuals. (ens-lyon.fr)
  • HBV), and hepatitis C virus (HCV). (nih.gov)
  • Blood donors in Australia who test positive for transfusion-transmissible infections, including human T-lymphotropic virus (HTLV), hepatitis B virus (HBV), hepatitis C virus, and HIV, undergo posttest counseling, as previously described ( 1 ). (cdc.gov)
  • Objective Despite dramatic increases in the misuse of prescription opioids, the extent to which their intravenous injection places drug users at risk of acquiring hepatitis C virus (HCV) remains unclear. (bmj.com)
  • This collection of monographs on selected viruses provide cancer hazard evaluations for the following human viruses: Epstein-Barr virus, Kaposi sarcoma-associated herpesvirus, human immunodeficiency virus-1, human T-cell lymphotropic virus type 1, and Merkel cell polyomavirus for potential listing in the Report on Carcinogens (RoC). (nih.gov)
  • Herpesvirus infections, such as those induced by human cytomegalovirus (HCMV), induce specific DNA damages. (springer.com)
  • The viruses that induce cellular DNA damage include members of the herpesvirus group, adenovirus, mumps-virus, measles-virus, rubella-virus, poliovirus and papilloma-virus (Fortunato et al. (springer.com)
  • Simian T-lymphotropic virus type 1 (STLV-1) strains compared with central Africa, human infections with occasionally infect humans. (cdc.gov)
  • However, the frequency of such viruses closely related to local STLV-1 strains are much infections is unknown. (cdc.gov)
  • T-lymphotropic virus type 1 infections in rural Côte d'Ivoire, direct zoonotic transmissions in a rural region of Côte where primate hunting is common. (cdc.gov)
  • Although the majority of HTLV-1 carriers remain asymptomatic, the virus is associated with severe diseases that can be subdivided into three categories: neoplastic diseases (adult T-cell leukaemia/lymphoma), inflammatory syndromes (HTLV-1-associated myelopathy/tropical spastic paraparesis and uveitis among others), and opportunistic infections (including Strongyloides stercoralis hyperinfection and others). (nih.gov)
  • Although most HTLV-1-infected individuals are asymptomatic, fetal and childhood infections often result in several diseases with disappointing treatment outcomes. (e-cep.org)
  • A parasitic male exists, but it is found only in experimentally infected dogs and has no role in human infections. (medscape.com)
  • The World Health Organization (WHO) estimates that blood donations up to 13 million units of the global blood supply, mainly in low or medium Human Development Index countries, are not screened for all relevant transfusion-transmissible infections [3]. (who.int)
  • Detection of HIV-1 and HCV infections among antibody-negative blood donors by nucleic acidamplification testing. (medigraphic.com)
  • Virus Type 1 in circulating among local nonhuman primate prey ( 3 ). (cdc.gov)
  • online Technical Appendix, wwwnc.cdc.gov/ strains and simian T-lymphotropic virus type 1 (STLV-1) EID/pdfs/11-1663-Techapp.pdf). (cdc.gov)
  • Brazil may have the highest absolute number of individuals infected by human T cell lymphotropic virus type 1 (HTLV-1). (karger.com)
  • Upon antiretroviral therapy (ART) human immunodeficiency virus (HIV)/human T-cell lymphotropic virus type 1 (HTLV-1) co-infected individuals frequently develop neurological disorders through hitherto unknown mechanisms. (ens-lyon.fr)
  • In November 1985, a blood donor at a Colorado blood-collection center was found to be seropositive for human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV)* antibody by both the enzyme-linked immunosorbent assay (ELISA) and Western blot methods. (cdc.gov)
  • Human T-cell lymphotropic viruses type 1 and 2 are retroviruses that share the same routes of transmission as HIV-1. (medscape.com)
  • However, prevalence rates of coinfection differ for distinct populations and regions of the world or for each virus, with human T-cell lymphotropic virus type 1 being more prevalent among HIV-1-infected individuals in the Southern hemisphere, while type 2 is more frequently found in the Northern hemisphere. (medscape.com)
  • In common, they share the tropism for T-lymphocytes, although human T-cell lymphotropic virus type 1 and HIV-1 are predominantly CD4 + T-cell tropic and human T-cell lymphotropic virus type 2 preferentially infects CD8 + cells. (medscape.com)
  • The available evidence suggests a protective role for coinfection by human T-cell lymphotropic virus type 2 on AIDS progression. (medscape.com)
  • This hypothesis is supported by several laboratory evidences, as well as by a number of clinical studies that found no significant interaction between human T-cell lymphotropic virus type 2 and HIV-1, or even detected a protective effect on HIV-1 disease. (medscape.com)
  • A common finding in coinfection by both human T-cell lymphotropic virus type 1 and 2 is the increase in CD4 + cell count, but without any additional immune benefit for patients. (medscape.com)
  • Mise en évidence de structures de type "biofilm ", formées par le rétrovirus HTLV-1 générés par des cellules infectées (cellules du haut), qui ont été transmis à un autre lymphocyte (cellule du bas). (pasteur.fr)
  • Human T-lymphotropic virus type 1 (HTLV-1) is the etiological agent of a slowly progressive neurodegenerative disease, HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis (HAM/TSP). (pasteur.fr)
  • However, RNA interference studies have shown that depletion of IRF4, rather than of IRF7, dramatically decreases the endogenous level of BIC by up to 70% in EBV- or human T-cell leukemia virus type 1 (HTLV1)-transformed cell lines and results in apoptosis and reduction of proliferation rates that are restored by transient expression of miR-155. (nih.gov)
  • Interest is increasing in human T-cell lymphotropic virus type-1 (HTLV-1) transmission due to its adverse health impacts. (e-cep.org)
  • The second type of life cycle allows noninfective new larvae to molt in the human host into infective filariform larvae. (medscape.com)
  • ATL is a rare and aggressive type of cancer that disrupts the body's ability to control the HTLV-1 virus. (nih.gov)
  • 1. Cutaneous type of adult T cell leukemia/lymphoma: a new entity among cutaneous lymphomas. (nih.gov)
  • 2. Human T-lymphotropic virus type I proviral loads in patients with adult T-cell leukemia-lymphoma: Comparison between cutaneous type and other subtypes. (nih.gov)
  • 3. New entity, definition and diagnostic criteria of cutaneous adult T-cell leukemia/lymphoma: human T-lymphotropic virus type 1 proviral DNA load can distinguish between cutaneous and smoldering types. (nih.gov)
  • 7. Lymphoma-type adult T-cell leukaemia-lymphoma with a bulky cutaneous tumour showing multiple human T-lymphotropic virus-1 DNA integration. (nih.gov)
  • 11. The role of human T cell lymphotropic virus type I tax in the development of cutaneous T cell lymphoma. (nih.gov)
  • 13. Absence of human T-lymphotropic virus type I in Japanese patients with cutaneous T-cell lymphoma. (nih.gov)
  • Saeed Z, Rowan A, Greiller C, Taylor GP, Pollock K. Enhanced T-cell maturation and monocyte aggregation are features of cellular inflammation in human T-lymphotropic virus type-1-associated myelopathy. (imperial.ac.uk)
  • Cost-effectiveness of human T-lymphotropic virus type 1 ( HTLV -1) antenatal screening in the United Kingdom. (imperial.ac.uk)
  • Incidence and risk factors for human T-lymphotropic virus type II seroconversion among injecting drug users in Baltimore, Maryland, U.S.A. (bgu.ac.il)
  • To determine the incidence of and risk factors for human T-lymphotropic virus, type II (HTLV-II) seroconversion among injecting drug users (IDUs), specimens from IDUs recruited into the ALIVE Study in 1988/1989 were assayed at baseline for antibody to HTLV with use of enzyme immunoassay and Western blot. (bgu.ac.il)
  • Dive into the research topics of 'Incidence and risk factors for human T-lymphotropic virus type II seroconversion among injecting drug users in Baltimore, Maryland, U.S.A.'. Together they form a unique fingerprint. (bgu.ac.il)
  • Incidence and risk factors for human T-lymphotropic virus type II seroconversion among injecting drug users in Baltimore, Maryland, U.S.A. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology , 9 (1), 89-96. (bgu.ac.il)
  • One patient had metastatic adenocarcinoma, one had diabetes and unexplained thrombocytopenia, while another had human T-cell lymphotropic virus type 1-associated tropical spastic paraparesis. (medscape.com)
  • Plasmapheresis in treatment of human T-lymphotropic virus type-I associated myelopathy. (qxmd.com)
  • In 11 of 18 patients with human T-lymphotropic virus type-I (HTLV-I) associated myelopathy (HAM) gait, sensory, and/or sphincter disturbance improved with plasmapheresis (4 to 6 sessions in 2 weeks), and the effects were maintained for 2 to 4 weeks. (qxmd.com)
  • Adult T-cell leukemia (ATL) is usually defined as a malignant disease of T cells infected by human T-lymphotropic virus type I (HTLV-I). In the present study, we describe a 49-year-old woman with an acute type ATL, whose leukemic cells do not contain the HTLV-I genome. (karger.com)
  • Tanaka A, Takahashi C, Yamaoka S, Nosaka T, Maki M, Hatanaka M: Oncogenic transformation by the Tax gene of human T-cell leukemia virus type I in vitro. (karger.com)
  • Shimoyama M, Kagami Y, Shimotohno K, Miwa M, Minato K, Tobinai K, Suematsu K, Sugimura T: Adult T-cell leukemia/lymphoma not associated with human T-cell leukemia virus type I. Proc Natl Acad Sci USA 1986;83:4524-4528. (karger.com)
  • Induction of CD4+, human T lymphotropic virus type-1-specific cytotoxic T lymphocytes from patients with HAM/TSP. (aai.org)
  • Recognition of an immunogenic region of the gp46 envelope glycoprotein of human T lymphotropic virus type-1. (aai.org)
  • The HTLV-1 type is subdivided into seven subtypes and HTLV-2 in four. (fiocruz.br)
  • 1-associated myelopathy or tropical spastic paraparesis. (cdc.gov)
  • Tropical spastic paraparesis and HTLV-1 associated myelopathy: clinical, epidemiological, virological and therapeutic aspects. (nih.gov)
  • The majority of HTLV-1 infected patients are considered as HTLV-1 carriers, but 5% will develop HTLV-1 associated myelopathy (HAM) and about 15% overactive bladder, an oligosymptomatic form of HAM. (biomedcentral.com)
  • Seroprevalence data collected from Peruvian female sex workers (FSWs) working in Callao over three study periods between 1993 and 2010 were used to examine the secular trend in HTLV-1 prevalence. (edu.pe)
  • it is to be used by all states for AIDS case reporting effective January 1, 1993. (cdc.gov)
  • abstract = "The development of B-cell lymphomas has been seldom described in HTLV-1 carriers. (edu.pe)
  • abstract = "We demonstrate here that TPA activates HTLV-1 LTR expression in Jurkat and H9 T-cell lines, by strictly different mechanisms. (bgu.ac.il)
  • Like HIV, HTLV-1 predominantly infects CD4+ T cells. (wikipedia.org)
  • HTLV-1 infects mainly T cells, leading to activation and cellular proliferation with exaggerated production of pro-inflammatory cytokines. (biomedcentral.com)
  • The virus infects mature T lymphocytes in vitro, although other cells can serve as targets. (aao.org)
  • [ 1 ] This discovery was the first formal proof that human retroviruses exist and suggested their etiological role in human cancer, a hypothesis that had been proposed decades before. (medscape.com)
  • Currently, the main focus of LMM scientists is murine (e.g., murine leukemia virus) and primate retroviruses (e.g. (nih.gov)
  • There is no human genome project yet, but we know that there are endogenous retroviruses in human DNA. (scienceblogs.com)
  • This section provides background information on the preparation of the monographs as well as a discussion of overarching issues related to evaluating the evidence for cancer from human epidemiological studies and evaluating the causation by viruses. (nih.gov)
  • In Africa the prevalence is not well known, but it is about 1% in some countries. (wikipedia.org)
  • It has been suggested that the prevalence of HTLV-1 is increased in patients with skin diseases. (karger.com)
  • Although India and Pakistan are not known to be geographic risk areas for HTLV-1, few prevalence studies are available ( 4 ), and HTLV-1 is commonly present in small geographic foci ( 5 ). (cdc.gov)
  • HTLV-1 prevalence in pregnant women , the risk of HTLV-1 transmission when breastfeeding lasts for 6 months or more, and the cost of screening tests were the variables with the largest effect on ICER. (bvsalud.org)
  • HTLV-1 is endemic in Peru, with the highest prevalence reported among commercial sex workers. (edu.pe)
  • This is a cross-sectional study, in which the prevalence of tuberculosis was analyzed in 166 HTLV-1 infected individuals. (biomedcentral.com)
  • This study aimed to conduct a pooled estimate of HTLV-1 prevalence among pregnant women in Nigeria to quantify its clinical burden and public health implications. (e-cep.org)
  • Our decade-old subgroup analysis found inconsistencies in the HTLV-1 prevalence. (e-cep.org)
  • The human t-lymphotropic virus market in the Netherlands can expand or contract due to a variety of reasons including population demographics, disease incidence and prevalence, macroeconomic issues, and geopolitical considerations. (medicaldevice-network.com)
  • Prevalence of HIV-1 in blood donations following implementation of a structured blood safety policy in South Africa. (medigraphic.com)
  • Incidence and estimated rates of residual risk for HIV, hepatitis C, hepatitis B and human T-cell lymphotropic viruses in blood donors in Canada, 1990- 2000. (medigraphic.com)
  • Of those 6 subtypes, 5 are STLV-1 sequences by using a tax -specifi c quantitative mainly found in or endemic to central Africa: HTLV-1B, PCR ( 8 ). (cdc.gov)
  • This study confirms that HTLV-1 is highly endemic to central Australia. (nt.gov.au)
  • Overrepresentation of patients from HTLV-1 endemic countries among peripheral T-cell lymphomas in the Netherlands: an indication of under-diagnosis of Adult T cell leukaemia/lymphoma. (imperial.ac.uk)
  • For example, IARC considers there to be strong evidence that both tobacco smoking and eating processed meat can cause cancer, so both are listed as "carcinogenic to humans. (cancer.org)
  • The agent (mixture) is carcinogenic to humans. (wikidoc.org)
  • The exposure circumstance entails exposures that are carcinogenic to humans. (wikidoc.org)
  • These lists also do not include substances evaluated as "not classifiable as to its carcinogenicity in humans. (cancer.org)
  • This category is used when there is sufficient evidence of carcinogenicity in humans. (wikidoc.org)
  • Exceptionally, an agent (mixture) may be placed in this category when evidence of carcinogenicity in humans is less than sufficient but there is sufficient evidence of carcinogenicity in experimental animals and strong evidence in exposed humans that the agent (mixture) acts through a relevant mechanism of carcinogenicity. (wikidoc.org)
  • This disease develops upon infiltration of HTLV-1-infected lymphocytes into the central nervous system, mostly at the thoracic spinal cord level. (pasteur.fr)
  • Current studies focus on many factors involved in the interaction of HTLV-1 infected lymphocytes with the BBB endothelium. (pasteur.fr)
  • Infected T lymphocytes that are transformed by HTLV-1 into malignant ATL cell have constitutively activated Interleukin-2 (IL-2), IL-9 and IL-15 production pathways that function as autocrine and paracrine stimulators of these cells by stimulating these cells through the Janus Kinase (JAK) 1 and 3/Signal transducer and activator of transcription 5 (STAT5) pathways. (nih.gov)
  • 1 Mycosis fungoides (MF) and Sézary syndrome (SS) are the two major clinical variants of CTCL, both characterised by epidermotropic infiltrates of clonal malignant lymphocytes with cerebriform nuclei. (bmj.com)
  • Differentiation of human T lymphocytes. (aai.org)
  • Excerpted from BCSC 2020-2021 series: Section 1 - Update on General Medicine . (aao.org)
  • History of self-flagellation was elicited in 7 (28%) of 25 HTLV-1-positive donors identified during January 2012-December 2018. (cdc.gov)
  • Here, we show that effective anti-HIV ART increases HTLV-1 proviral load through a polyclonal integration pattern of HTLV-1 in both CD4(+) and CD8(+) T-cell subsets that is reminiscent of that typically associated with HTLV-1-related inflammatory conditions. (ens-lyon.fr)
  • p21 plays an essential role in growth arrest after DNA damage ( 19 - 21 ), and overexpression leads to G 1 and G 2 ( 22 ) or S-phase ( 23 ) arrest. (aacrjournals.org)
  • Once integrated, HTLV-1 continues to exist only as a provirus which can spread from cell to cell through a viral synapse. (wikipedia.org)
  • Human cytomegalovirus (HCMV) is a member of the betaherpesvirus subfamily and encodes more than 200 viral proteins (Chee et al. (springer.com)
  • The adult female worm lives in tunnels between the enterocytes in the small bowel of humans. (medscape.com)
  • Only adult females are found in infected humans. (medscape.com)
  • The human T-cell leukemia virus 1 (HTLV-1) causes adult T-cell leukemia (ATL). (nih.gov)
  • 8. Human T-lymphotropic virus 1 associated with adult T-cell leukemia/lymphoma. (nih.gov)
  • 17. HTLV-1 and associated adult T-cell leukemia/lymphoma. (nih.gov)
  • The purified immunoglobulin is derived from pooled adult human plasma selected for high titers of antibody for Cytomegalovirus (CMV) (1). (theodora.com)
  • The main skin diseases described in HTLV-1 seropositives were vitiligo (2 cases), dermatophytosis (2 cases), and leprosy (2 cases). (karger.com)
  • These studies and others detailing pathological roles of IL-17 in human diseases eventually culminated in the development of monoclonal antibodies (mAbs) that target IL-17A, both IL-17A and IL-17F, IL-17RA, or IL-23, a cytokine produced by innate immune cells that promotes the expansion of T H 17 cell populations. (nature.com)
  • Although HTLV-1 has spread globally, its geographic such as hunting of nonhuman primates or consumption of distribution is not uniform. (cdc.gov)
  • Active cyclin/Cdk complexes phosphorylate and inactivate members of the retinoblastoma protein (Rb) family that are negative regulators of G 1 and S-phase progression, leading to induction of E2F-regulated gene expression and cell proliferation. (aacrjournals.org)
  • Description: HTLV-1 P24 Protein [His], recombinant protein from E. coli. (bioinfogenome.net)
  • I. Acquisition of a novel human cell surface protein (p80) during normal intrathymic T cell maturation. (aai.org)
  • Human T-cell lymphotropic virus (HTLV) and its subtypes were estimated to have infected 5-10 million people worldwide [ 1 - 3 ]. (e-cep.org)
  • HIV has 2 subtypes, HIV-1 and HIV-2. (aao.org)
  • We present the case of an elderly Peruvian HTLV-1 carrier who was diagnosed with EBV-positive diffuse large B-cell lymphoma. (edu.pe)
  • In this elderly patient, the combination of EBV and HTLV-1 coinfection and immunosenescence may have played a role in the development of this aggressive diffuse large B-cell lymphoma. (edu.pe)
  • Rowe M, Rooney CM, Edwards CF, Lenior GM, Rickinson AB: Epstein-Barr virus status and tumor cell phenotype in sporadic Burkitt's lymphoma. (karger.com)
  • It appears from literature that human cytomegalovirus enhances DNA repair capacity in host cells, without producing detectable lesions in cellular DNA or inhibiting DNA synthesis (Nishiyama and Rapp 1981 ). (springer.com)
  • In 2022, GlobalData's Market Model methodology determined that the leading player in the human t-lymphotropic virus market in the Netherlands was Abbott Laboratories followed by DiaSorin , F. Hoffmann-La Roche , HU Group , MP Biomedicals and Werfen Life Group SAU. (medicaldevice-network.com)
  • CytoGam®, Cytomegalovirus Immune Globulin Intravenous (Human) (CMV-IGIV), is an immunoglobulin G (IgG) containing a standardized amount of antibody to Cytomegalovirus (CMV). (theodora.com)
  • This classification system replaces the system published by CDC in 1986 (1) and is primarily intended for use in public health practice. (cdc.gov)
  • These pathologies are a serious threat to the several million and completed questionnaires aimed at determining their persons infected with HTLV-1 ( 1 ). (cdc.gov)
  • Although T cell receptor (TCR) activation is key for IL-17 production by CD4 + and CD8 + T cells, IL-17 production by innate immune cells is primarily driven by inflammatory cytokines, especially IL-1β and IL-23 (Box 2 ). (nature.com)
  • In 1979, HTLV-1 was isolated for the first time from a patient with a T-cell malignancy. (medscape.com)
  • There were no cases of HTLV-1 detected among FSW born after 1979 (N = 224). (edu.pe)
  • humans are infected with HTLV-1A, the only human- restricted molecular subtype ( 6-9 ). (cdc.gov)
  • Tang AR, Taylor GP, Dhasmana D. Self-flagellation and blood borne virus transmission: A case series. (imperial.ac.uk)
  • HIV is a blood-borne virus and is transmitted via sexual intercourse, shared intravenous drug paraphernalia, blood transfusion, and from mother to child during birth or breastfeeding. (aao.org)
  • The knowledge about HTLV-1 epidemiology is limited. (wikipedia.org)
  • The RoC contains a list of identified substances (i) that either are known to be human carcinogens or are reasonably anticipated to be human carcinogens and (ii) to which a significant number of persons residing in the United States are exposed. (nih.gov)
  • More information on each of these known and probable human carcinogens can be found on their websites. (cancer.org)
  • These lists include agents that have been classified as known or probable human carcinogens. (cancer.org)
  • for reactivity to HTLV-1/2 antigens ( 10 ). (cdc.gov)
  • Three main factors determine the efficiency of anti-HCV diagnostics: 1) target antigens used in the assay design, 2) professional skill of the technician performing the assay, and 3) laboratory environment. (who.int)
  • The cancer hazard evaluation component provides the following information relevant to a RoC listing recommendation: Properties and Detection (Section 1), Human Exposure (Section 2), Human Cancer Studies (Section 3), Mechanistic and Other Relevant Data (Section 4), and Overall Cancer Hazard Evaluation and Preliminary Listing Recommendation (Section 5). (nih.gov)
  • In Jurkat cells this activation is exerted by a PKCα- and PKCε-antagonized mechanism which operates through an Sp1 binding site residing within the Est responsive region 1 of the LTR. (bgu.ac.il)
  • Chamias, R , Huleihel, M & Aboud, M 2010, ' The mechanism of HTLV-1 LTR activation by TPA varies in different human T-cell lines: Role of specific PKC isoforms ', Leukemia Research , vol. 34, no. 1, pp. 93-99. (bgu.ac.il)
  • [ 20 , 21 ] When the causal agent of AIDS was isolated by the same group that discovered HTLV-1 and HTLV-2, they thought it was a third member of the HTLV family. (medscape.com)
  • In the report of 181 patients (largely Japanese) in the French-language literature, 4 cases were associated with carcinoma of the stomach, 3 with carcinoma of the liver, 1 with carcinoma of the lung, 3 with unspecified malignant tumors. (medscape.com)
  • A patient infected with HTLV can be diagnosed when antibodies against HTLV-1 are detected in the serum. (wikipedia.org)
  • Patients must have serum antibodies directed to HTLV-1. (nih.gov)
  • The Htlv-1 P19 Elisa Kit reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. (bioinfogenome.net)
  • Description: A competitive ELISA for quantitative measurement of Human True insulin in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. (bioinfogenome.net)
  • In Europe HTLV-1 is still uncommon, although it is present in some high-risk populations, including immigrants and intravenous drug users. (wikipedia.org)
  • Cytomegalovirus Immune Globulin Intravenous (Human) is indicated for the prophylaxis of cytomegalovirus disease associated with transplantation of kidney, lung, liver, pancreas and heart. (theodora.com)
  • In this setting, unlike in other intestinal nematodes of humans, the larvae can increase in numbers without reinfection from outside. (medscape.com)
  • These data indicate that preventing ART-triggered clonal expansion of HTLV-1-infected cells in co-infected individuals deserves investigation. (ens-lyon.fr)
  • Correspondingly, the endogenous levels of IRF4 and -7 are correlated with that of the BIC transcript in Epstein-Barr virus (EBV)-transformed cells. (nih.gov)
  • The control aspects of the five DNA repair mechanisms in virus-infected cells have not been well characterized. (springer.com)
  • IL-17A and IL-17F are produced by CD4 + and CD8 + T cells, γδ T cells, and various innate immune cell populations in response to IL-1β and IL-23, and they mediate protective immunity against fungi and bacteria by promoting neutrophil recruitment, antimicrobial peptide production and enhanced barrier function. (nature.com)
  • White blood cells released by the bone marrow that circulate in the peripheral blood account for only 5% of the total WBC mass and form two pools of cells: (1) marginal and (2) circulating. (pocketdentistry.com)
  • The only human genotype that does not have a simian relative is A. It is thought that genotypes B, D, E, F and G originated in Africa from closely related STLV about 30,000 years ago, while the Asian genotype C is thought to have originated independently in Indonesia from the simians present there. (wikipedia.org)