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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2019-02-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-08534-1 |
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doaj-5f068cea4ece4349a43cb5cd50da36002021-05-11T12:24:04ZengNature Publishing GroupNature Communications2041-17232019-02-011011910.1038/s41467-019-08534-1Virus-specific memory T cells populate tumors and can be repurposed for tumor immunotherapyPamela C. Rosato0Sathi Wijeyesinghe1J. Michael Stolley2Christine E. Nelson3Rachel L. Davis4Luke S. Manlove5Christopher A. Pennell6Bruce R. Blazar7Clark C. Chen8Melissa A. Geller9Vaiva Vezys10David Masopust11Department of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Laboratory Medicine and Pathology, Center for Immunology, University of MinnesotaDepartment of Pediatrics, Center for Immunology, University of MinnesotaDepartment of Neurosurgery, University of MinnesotaDepartment of Obstetrics, Gynecology and Women’s Health, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaDepartment of Microbiology and Immunology, Center for Immunology, University of MinnesotaThe 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.https://doi.org/10.1038/s41467-019-08534-1 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
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 |
spellingShingle |
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 Nature Communications |
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 Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2019-02-01 |
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. |
url |
https://doi.org/10.1038/s41467-019-08534-1 |
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