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Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection
Therapeutic vaccination is a potentially promising strategy to enhance T cell immunity and viral control in chronically infected individuals. However, therapeutic vaccination approaches have fallen short of expectations, and effective boosting of antiviral T cell responses has not always been observ...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275378/ https://www.ncbi.nlm.nih.gov/pubmed/18332181 http://dx.doi.org/10.1084/jem.20071949 |
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author | Ha, Sang-Jun Mueller, Scott N. Wherry, E. John Barber, Daniel L. Aubert, Rachael D. Sharpe, Arlene H. Freeman, Gordon J. Ahmed, Rafi |
author_facet | Ha, Sang-Jun Mueller, Scott N. Wherry, E. John Barber, Daniel L. Aubert, Rachael D. Sharpe, Arlene H. Freeman, Gordon J. Ahmed, Rafi |
author_sort | Ha, Sang-Jun |
collection | PubMed |
description | Therapeutic vaccination is a potentially promising strategy to enhance T cell immunity and viral control in chronically infected individuals. However, therapeutic vaccination approaches have fallen short of expectations, and effective boosting of antiviral T cell responses has not always been observed. One of the principal reasons for the limited success of therapeutic vaccination is that virus-specific T cells become functionally exhausted during chronic infections. We now provide a novel strategy for enhancing the efficacy of therapeutic vaccines. In this study, we show that blocking programmed death (PD)-1/PD-L1 inhibitory signals on exhausted CD8(+) T cells, in combination with therapeutic vaccination, synergistically enhances functional CD8(+) T cell responses and improves viral control in mice chronically infected with lymphocytic choriomeningitis virus. This combinatorial therapeutic vaccination was effective even in the absence of CD4(+) T cell help. Thus, our study defines a potent new approach to augment the efficacy of therapeutic vaccination by blocking negative signals. Such an approach may have broad applications in developing treatment strategies for chronic infections in general, and perhaps also for tumors. |
format | Text |
id | pubmed-2275378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22753782008-09-17 Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection Ha, Sang-Jun Mueller, Scott N. Wherry, E. John Barber, Daniel L. Aubert, Rachael D. Sharpe, Arlene H. Freeman, Gordon J. Ahmed, Rafi J Exp Med Articles Therapeutic vaccination is a potentially promising strategy to enhance T cell immunity and viral control in chronically infected individuals. However, therapeutic vaccination approaches have fallen short of expectations, and effective boosting of antiviral T cell responses has not always been observed. One of the principal reasons for the limited success of therapeutic vaccination is that virus-specific T cells become functionally exhausted during chronic infections. We now provide a novel strategy for enhancing the efficacy of therapeutic vaccines. In this study, we show that blocking programmed death (PD)-1/PD-L1 inhibitory signals on exhausted CD8(+) T cells, in combination with therapeutic vaccination, synergistically enhances functional CD8(+) T cell responses and improves viral control in mice chronically infected with lymphocytic choriomeningitis virus. This combinatorial therapeutic vaccination was effective even in the absence of CD4(+) T cell help. Thus, our study defines a potent new approach to augment the efficacy of therapeutic vaccination by blocking negative signals. Such an approach may have broad applications in developing treatment strategies for chronic infections in general, and perhaps also for tumors. The Rockefeller University Press 2008-03-17 /pmc/articles/PMC2275378/ /pubmed/18332181 http://dx.doi.org/10.1084/jem.20071949 Text en Copyright © 2008, 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 Ha, Sang-Jun Mueller, Scott N. Wherry, E. John Barber, Daniel L. Aubert, Rachael D. Sharpe, Arlene H. Freeman, Gordon J. Ahmed, Rafi Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title | Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title_full | Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title_fullStr | Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title_full_unstemmed | Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title_short | Enhancing therapeutic vaccination by blocking PD-1–mediated inhibitory signals during chronic infection |
title_sort | enhancing therapeutic vaccination by blocking pd-1–mediated inhibitory signals during chronic infection |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275378/ https://www.ncbi.nlm.nih.gov/pubmed/18332181 http://dx.doi.org/10.1084/jem.20071949 |
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