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Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover
The key attributes of CD8(+) T cell protective immunity in human immunodeficiency virus (HIV) infection remain unclear. We report that CD8(+) T cell responses specific for Gag and, in particular, the immunodominant p24 epitope KK10 correlate with control of HIV-1 replication in human histocompatibil...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118466/ https://www.ncbi.nlm.nih.gov/pubmed/17893201 http://dx.doi.org/10.1084/jem.20070784 |
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author | Almeida, Jorge R. Price, David A. Papagno, Laura Arkoub, Zaïna Aït Sauce, Delphine Bornstein, Ethan Asher, Tedi E. Samri, Assia Schnuriger, Aurélie Theodorou, Ioannis Costagliola, Dominique Rouzioux, Christine Agut, Henri Marcelin, Anne-Geneviève Douek, Daniel Autran, Brigitte Appay, Victor |
author_facet | Almeida, Jorge R. Price, David A. Papagno, Laura Arkoub, Zaïna Aït Sauce, Delphine Bornstein, Ethan Asher, Tedi E. Samri, Assia Schnuriger, Aurélie Theodorou, Ioannis Costagliola, Dominique Rouzioux, Christine Agut, Henri Marcelin, Anne-Geneviève Douek, Daniel Autran, Brigitte Appay, Victor |
author_sort | Almeida, Jorge R. |
collection | PubMed |
description | The key attributes of CD8(+) T cell protective immunity in human immunodeficiency virus (HIV) infection remain unclear. We report that CD8(+) T cell responses specific for Gag and, in particular, the immunodominant p24 epitope KK10 correlate with control of HIV-1 replication in human histocompatibility leukocyte antigen (HLA)–B27 patients. To understand further the nature of CD8(+) T cell–mediated antiviral efficacy, we performed a comprehensive study of CD8(+) T cells specific for the HLA-B27–restricted epitope KK10 in chronic HIV-1 infection based on the use of multiparametric flow cytometry together with molecular clonotypic analysis and viral sequencing. We show that B27-KK10–specific CD8(+) T cells are characterized by polyfunctional capabilities, increased clonal turnover, and superior functional avidity. Such attributes are interlinked and constitute the basis for effective control of HIV-1 replication. These data on the features of effective CD8(+) T cells in HIV infection may aid in the development of successful T cell vaccines. |
format | Text |
id | pubmed-2118466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21184662008-04-01 Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover Almeida, Jorge R. Price, David A. Papagno, Laura Arkoub, Zaïna Aït Sauce, Delphine Bornstein, Ethan Asher, Tedi E. Samri, Assia Schnuriger, Aurélie Theodorou, Ioannis Costagliola, Dominique Rouzioux, Christine Agut, Henri Marcelin, Anne-Geneviève Douek, Daniel Autran, Brigitte Appay, Victor J Exp Med Articles The key attributes of CD8(+) T cell protective immunity in human immunodeficiency virus (HIV) infection remain unclear. We report that CD8(+) T cell responses specific for Gag and, in particular, the immunodominant p24 epitope KK10 correlate with control of HIV-1 replication in human histocompatibility leukocyte antigen (HLA)–B27 patients. To understand further the nature of CD8(+) T cell–mediated antiviral efficacy, we performed a comprehensive study of CD8(+) T cells specific for the HLA-B27–restricted epitope KK10 in chronic HIV-1 infection based on the use of multiparametric flow cytometry together with molecular clonotypic analysis and viral sequencing. We show that B27-KK10–specific CD8(+) T cells are characterized by polyfunctional capabilities, increased clonal turnover, and superior functional avidity. Such attributes are interlinked and constitute the basis for effective control of HIV-1 replication. These data on the features of effective CD8(+) T cells in HIV infection may aid in the development of successful T cell vaccines. The Rockefeller University Press 2007-10-01 /pmc/articles/PMC2118466/ /pubmed/17893201 http://dx.doi.org/10.1084/jem.20070784 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Almeida, Jorge R. Price, David A. Papagno, Laura Arkoub, Zaïna Aït Sauce, Delphine Bornstein, Ethan Asher, Tedi E. Samri, Assia Schnuriger, Aurélie Theodorou, Ioannis Costagliola, Dominique Rouzioux, Christine Agut, Henri Marcelin, Anne-Geneviève Douek, Daniel Autran, Brigitte Appay, Victor Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title | Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title_full | Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title_fullStr | Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title_full_unstemmed | Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title_short | Superior control of HIV-1 replication by CD8(+) T cells is reflected by their avidity, polyfunctionality, and clonal turnover |
title_sort | superior control of hiv-1 replication by cd8(+) t cells is reflected by their avidity, polyfunctionality, and clonal turnover |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118466/ https://www.ncbi.nlm.nih.gov/pubmed/17893201 http://dx.doi.org/10.1084/jem.20070784 |
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