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Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production
In the present study, we have investigated the distribution of HIV-specific and HIV-infected CD4 T cells within different populations of memory CD4 T cells isolated from lymph nodes of viremic HIV-infected subjects. Four memory CD4 T cell populations were identified on the basis of the expression of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549706/ https://www.ncbi.nlm.nih.gov/pubmed/23254284 http://dx.doi.org/10.1084/jem.20121932 |
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author | Perreau, Matthieu Savoye, Anne-Laure De Crignis, Elisa Corpataux, Jean-Marc Cubas, Rafael Haddad, Elias K. De Leval, Laurence Graziosi, Cecilia Pantaleo, Giuseppe |
author_facet | Perreau, Matthieu Savoye, Anne-Laure De Crignis, Elisa Corpataux, Jean-Marc Cubas, Rafael Haddad, Elias K. De Leval, Laurence Graziosi, Cecilia Pantaleo, Giuseppe |
author_sort | Perreau, Matthieu |
collection | PubMed |
description | In the present study, we have investigated the distribution of HIV-specific and HIV-infected CD4 T cells within different populations of memory CD4 T cells isolated from lymph nodes of viremic HIV-infected subjects. Four memory CD4 T cell populations were identified on the basis of the expression of CXCR5, PD-1, and Bcl-6: CXCR5(−)PD-1(−)Bcl-6(−), CXCR5(+)PD-1(−)Bcl-6(−), CXCR5(−)PD-1(+)Bcl-6(−), and CXCR5(+)PD-1(+)Bcl-6(+). On the basis of Bcl-6 expression and functional properties (IL-21 production and B cell help), the CXCR5(+)PD-1(+)Bcl-6(+) cell population was considered to correspond to the T follicular helper (Tfh) cell population. We show that Tfh and CXCR5(−)PD-1(+) cell populations are enriched in HIV-specific CD4 T cells, and these populations are significantly increased in viremic HIV-infected subjects as compared with healthy subjects. The Tfh cell population contained the highest percentage of CD4 T cells harboring HIV DNA and was the most efficient in supporting productive infection in vitro. Replication competent HIV was also readily isolated from Tfh cells in subjects with nonprogressive infection and low viremia (<1,000 HIV RNA copies). However, only the percentage of Tfh cells correlated with the levels of plasma viremia. These results demonstrate that Tfh cells serve as the major CD4 T cell compartment for HIV infection, replication, and production. |
format | Online Article Text |
id | pubmed-3549706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35497062013-07-14 Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production Perreau, Matthieu Savoye, Anne-Laure De Crignis, Elisa Corpataux, Jean-Marc Cubas, Rafael Haddad, Elias K. De Leval, Laurence Graziosi, Cecilia Pantaleo, Giuseppe J Exp Med Article In the present study, we have investigated the distribution of HIV-specific and HIV-infected CD4 T cells within different populations of memory CD4 T cells isolated from lymph nodes of viremic HIV-infected subjects. Four memory CD4 T cell populations were identified on the basis of the expression of CXCR5, PD-1, and Bcl-6: CXCR5(−)PD-1(−)Bcl-6(−), CXCR5(+)PD-1(−)Bcl-6(−), CXCR5(−)PD-1(+)Bcl-6(−), and CXCR5(+)PD-1(+)Bcl-6(+). On the basis of Bcl-6 expression and functional properties (IL-21 production and B cell help), the CXCR5(+)PD-1(+)Bcl-6(+) cell population was considered to correspond to the T follicular helper (Tfh) cell population. We show that Tfh and CXCR5(−)PD-1(+) cell populations are enriched in HIV-specific CD4 T cells, and these populations are significantly increased in viremic HIV-infected subjects as compared with healthy subjects. The Tfh cell population contained the highest percentage of CD4 T cells harboring HIV DNA and was the most efficient in supporting productive infection in vitro. Replication competent HIV was also readily isolated from Tfh cells in subjects with nonprogressive infection and low viremia (<1,000 HIV RNA copies). However, only the percentage of Tfh cells correlated with the levels of plasma viremia. These results demonstrate that Tfh cells serve as the major CD4 T cell compartment for HIV infection, replication, and production. The Rockefeller University Press 2013-01-14 /pmc/articles/PMC3549706/ /pubmed/23254284 http://dx.doi.org/10.1084/jem.20121932 Text en © 2013 Perreau et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article Perreau, Matthieu Savoye, Anne-Laure De Crignis, Elisa Corpataux, Jean-Marc Cubas, Rafael Haddad, Elias K. De Leval, Laurence Graziosi, Cecilia Pantaleo, Giuseppe Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title | Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title_full | Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title_fullStr | Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title_full_unstemmed | Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title_short | Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production |
title_sort | follicular helper t cells serve as the major cd4 t cell compartment for hiv-1 infection, replication, and production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549706/ https://www.ncbi.nlm.nih.gov/pubmed/23254284 http://dx.doi.org/10.1084/jem.20121932 |
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