Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy
The immunosuppressive tumor environment and the lack of functional anti-tumor immunity are major limiting factors in immunotherapy. Here the authors show that human and mouse tumors are infiltrated by virus-specific memory T cells, which can be harnessed by viral peptides to induce local and systemi...
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Nature Portfolio
2019
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oai:doaj.org-article:5f068cea4ece4349a43cb5cd50da36002021-12-02T16:51:00ZVirus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy10.1038/s41467-019-08534-12041-1723https://doaj.org/article/5f068cea4ece4349a43cb5cd50da36002019-02-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-08534-1https://doaj.org/toc/2041-1723The immunosuppressive tumor environment and the lack of functional anti-tumor immunity are major limiting factors in immunotherapy. Here the authors show that human and mouse tumors are infiltrated by virus-specific memory T cells, which can be harnessed by viral peptides to induce local and systemic anti-tumor immunity and synergize with checkpoint blockade.Pamela C. RosatoSathi WijeyesingheJ. Michael StolleyChristine E. NelsonRachel L. DavisLuke S. ManloveChristopher A. PennellBruce R. BlazarClark C. ChenMelissa A. GellerVaiva VezysDavid MasopustNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-9 (2019) |
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Science Q |
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Science Q Pamela C. Rosato Sathi Wijeyesinghe J. Michael Stolley Christine E. Nelson Rachel L. Davis Luke S. Manlove Christopher A. Pennell Bruce R. Blazar Clark C. Chen Melissa A. Geller Vaiva Vezys David Masopust Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
description |
The immunosuppressive tumor environment and the lack of functional anti-tumor immunity are major limiting factors in immunotherapy. Here the authors show that human and mouse tumors are infiltrated by virus-specific memory T cells, which can be harnessed by viral peptides to induce local and systemic anti-tumor immunity and synergize with checkpoint blockade. |
format |
article |
author |
Pamela C. Rosato Sathi Wijeyesinghe J. Michael Stolley Christine E. Nelson Rachel L. Davis Luke S. Manlove Christopher A. Pennell Bruce R. Blazar Clark C. Chen Melissa A. Geller Vaiva Vezys David Masopust |
author_facet |
Pamela C. Rosato Sathi Wijeyesinghe J. Michael Stolley Christine E. Nelson Rachel L. Davis Luke S. Manlove Christopher A. Pennell Bruce R. Blazar Clark C. Chen Melissa A. Geller Vaiva Vezys David Masopust |
author_sort |
Pamela C. Rosato |
title |
Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
title_short |
Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
title_full |
Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
title_fullStr |
Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
title_full_unstemmed |
Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapy |
title_sort |
virus-specific memory t cells populate tumors and can be repurposed for tumor immunotherapy |
publisher |
Nature Portfolio |
publishDate |
2019 |
url |
https://doaj.org/article/5f068cea4ece4349a43cb5cd50da3600 |
work_keys_str_mv |
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