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Association of MHC-I genotypes with disease progression in HIV/SIV infections

Virus-specific cytotoxic T lymphocytes (CTLs) are major effectors in acquired immune responses against viral infection. Virus-specific CTLs recognize specific viral peptides presented by major histocompatibility complex class-I (MHC-I) on the surface of virus-infected target cells via their T cell r...

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Detalles Bibliográficos
Autores principales: Nomura, Takushi, Matano, Tetsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386493/
https://www.ncbi.nlm.nih.gov/pubmed/22754552
http://dx.doi.org/10.3389/fmicb.2012.00234
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author Nomura, Takushi
Matano, Tetsuro
author_facet Nomura, Takushi
Matano, Tetsuro
author_sort Nomura, Takushi
collection PubMed
description Virus-specific cytotoxic T lymphocytes (CTLs) are major effectors in acquired immune responses against viral infection. Virus-specific CTLs recognize specific viral peptides presented by major histocompatibility complex class-I (MHC-I) on the surface of virus-infected target cells via their T cell receptor (TCR) and eliminate target cells by both direct and indirect mechanisms. In human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infections, host immune responses fail to contain the virus and allow persistent viral replication, leading to AIDS progression. CTL responses exert strong suppressive pressure on HIV/SIV replication and cumulative studies have indicated association of HLA/MHC-I genotypes with rapid or slow AIDS progression.
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spelling pubmed-33864932012-07-02 Association of MHC-I genotypes with disease progression in HIV/SIV infections Nomura, Takushi Matano, Tetsuro Front Microbiol Microbiology Virus-specific cytotoxic T lymphocytes (CTLs) are major effectors in acquired immune responses against viral infection. Virus-specific CTLs recognize specific viral peptides presented by major histocompatibility complex class-I (MHC-I) on the surface of virus-infected target cells via their T cell receptor (TCR) and eliminate target cells by both direct and indirect mechanisms. In human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) infections, host immune responses fail to contain the virus and allow persistent viral replication, leading to AIDS progression. CTL responses exert strong suppressive pressure on HIV/SIV replication and cumulative studies have indicated association of HLA/MHC-I genotypes with rapid or slow AIDS progression. Frontiers Research Foundation 2012-06-29 /pmc/articles/PMC3386493/ /pubmed/22754552 http://dx.doi.org/10.3389/fmicb.2012.00234 Text en Copyright © Nomura and Matano. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) , which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Microbiology
Nomura, Takushi
Matano, Tetsuro
Association of MHC-I genotypes with disease progression in HIV/SIV infections
title Association of MHC-I genotypes with disease progression in HIV/SIV infections
title_full Association of MHC-I genotypes with disease progression in HIV/SIV infections
title_fullStr Association of MHC-I genotypes with disease progression in HIV/SIV infections
title_full_unstemmed Association of MHC-I genotypes with disease progression in HIV/SIV infections
title_short Association of MHC-I genotypes with disease progression in HIV/SIV infections
title_sort association of mhc-i genotypes with disease progression in hiv/siv infections
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386493/
https://www.ncbi.nlm.nih.gov/pubmed/22754552
http://dx.doi.org/10.3389/fmicb.2012.00234
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