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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...

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Detalles Bibliográficos
Autores principales: Freeman, Gordon J., Wherry, E. John, Ahmed, Rafi, Sharpe, Arlene H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
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.
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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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