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Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade
The programmed death (PD)-1–PD-1 ligand (PD-L) pathway, which is part of the B7–CD28 family, consists of the PD-1 receptor and its two ligands PD-L1 and PD-L2. Engagement of PD-1 by its ligands inhibits immune responses, and recent work has shown that PD-1 is highly expressed on exhausted T cells du...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118103/ https://www.ncbi.nlm.nih.gov/pubmed/17000870 http://dx.doi.org/10.1084/jem.20061800 |
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author | Freeman, Gordon J. Wherry, E. John Ahmed, Rafi Sharpe, Arlene H. |
author_facet | Freeman, Gordon J. Wherry, E. John Ahmed, Rafi Sharpe, Arlene H. |
author_sort | Freeman, Gordon J. |
collection | PubMed |
description | The programmed death (PD)-1–PD-1 ligand (PD-L) pathway, which is part of the B7–CD28 family, consists of the PD-1 receptor and its two ligands PD-L1 and PD-L2. Engagement of PD-1 by its ligands inhibits immune responses, and recent work has shown that PD-1 is highly expressed on exhausted T cells during chronic lymphocytic choriomeningitis virus (LCMV) infection in mice. Blockade of this pathway reinvigorates the exhausted T cells, allowing them to expand and produce effector cytokines, raising the issue of whether this pathway has been exploited by a variety of viruses during chronic infection. New studies now extend these observations to HIV infection and human disease. |
format | Text |
id | pubmed-2118103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21181032007-12-13 Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade Freeman, Gordon J. Wherry, E. John Ahmed, Rafi Sharpe, Arlene H. J Exp Med Commentaries The programmed death (PD)-1–PD-1 ligand (PD-L) pathway, which is part of the B7–CD28 family, consists of the PD-1 receptor and its two ligands PD-L1 and PD-L2. Engagement of PD-1 by its ligands inhibits immune responses, and recent work has shown that PD-1 is highly expressed on exhausted T cells during chronic lymphocytic choriomeningitis virus (LCMV) infection in mice. Blockade of this pathway reinvigorates the exhausted T cells, allowing them to expand and produce effector cytokines, raising the issue of whether this pathway has been exploited by a variety of viruses during chronic infection. New studies now extend these observations to HIV infection and human disease. The Rockefeller University Press 2006-10-02 /pmc/articles/PMC2118103/ /pubmed/17000870 http://dx.doi.org/10.1084/jem.20061800 Text en Copyright © 2006, 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 | Commentaries Freeman, Gordon J. Wherry, E. John Ahmed, Rafi Sharpe, Arlene H. Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title | Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title_full | Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title_fullStr | Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title_full_unstemmed | Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title_short | Reinvigorating exhausted HIV-specific T cells via PD-1–PD-1 ligand blockade |
title_sort | reinvigorating exhausted hiv-specific t cells via pd-1–pd-1 ligand blockade |
topic | Commentaries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118103/ https://www.ncbi.nlm.nih.gov/pubmed/17000870 http://dx.doi.org/10.1084/jem.20061800 |
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