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Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes
B cell follicles in secondary lymphoid tissues represent an immune privileged sanctuary for AIDS viruses, in part because cytotoxic CD8(+) T cells are mostly excluded from entering the follicles that harbor infected T follicular helper (T(FH)) cells. We studied the effects of native heterodimeric IL...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5825155/ https://www.ncbi.nlm.nih.gov/pubmed/29474450 http://dx.doi.org/10.1371/journal.ppat.1006902 |
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author | Watson, Dionysios C. Moysi, Eirini Valentin, Antonio Bergamaschi, Cristina Devasundaram, Santhi Fortis, Sotirios P. Bear, Jenifer Chertova, Elena Bess, Julian Sowder, Ray Venzon, David J. Deleage, Claire Estes, Jacob D. Lifson, Jeffrey D. Petrovas, Constantinos Felber, Barbara K. Pavlakis, George N. |
author_facet | Watson, Dionysios C. Moysi, Eirini Valentin, Antonio Bergamaschi, Cristina Devasundaram, Santhi Fortis, Sotirios P. Bear, Jenifer Chertova, Elena Bess, Julian Sowder, Ray Venzon, David J. Deleage, Claire Estes, Jacob D. Lifson, Jeffrey D. Petrovas, Constantinos Felber, Barbara K. Pavlakis, George N. |
author_sort | Watson, Dionysios C. |
collection | PubMed |
description | B cell follicles in secondary lymphoid tissues represent an immune privileged sanctuary for AIDS viruses, in part because cytotoxic CD8(+) T cells are mostly excluded from entering the follicles that harbor infected T follicular helper (T(FH)) cells. We studied the effects of native heterodimeric IL-15 (hetIL-15) treatment on uninfected rhesus macaques and on macaques that had spontaneously controlled SHIV infection to low levels of chronic viremia. hetIL-15 increased effector CD8(+) T lymphocytes with high granzyme B content in blood, mucosal sites and lymph nodes, including virus-specific MHC-peptide tetramer+ CD8(+) cells in LN. Following hetIL-15 treatment, multiplexed quantitative image analysis (histo-cytometry) of LN revealed increased numbers of granzyme B(+) T cells in B cell follicles and SHIV RNA was decreased in plasma and in LN. Based on these properties, hetIL-15 shows promise as a potential component in combination immunotherapy regimens to target AIDS virus sanctuaries and reduce long-term viral reservoirs in HIV-1 infected individuals. Trial registration: ClinicalTrials.gov NCT02452268 |
format | Online Article Text |
id | pubmed-5825155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58251552018-03-19 Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes Watson, Dionysios C. Moysi, Eirini Valentin, Antonio Bergamaschi, Cristina Devasundaram, Santhi Fortis, Sotirios P. Bear, Jenifer Chertova, Elena Bess, Julian Sowder, Ray Venzon, David J. Deleage, Claire Estes, Jacob D. Lifson, Jeffrey D. Petrovas, Constantinos Felber, Barbara K. Pavlakis, George N. PLoS Pathog Research Article B cell follicles in secondary lymphoid tissues represent an immune privileged sanctuary for AIDS viruses, in part because cytotoxic CD8(+) T cells are mostly excluded from entering the follicles that harbor infected T follicular helper (T(FH)) cells. We studied the effects of native heterodimeric IL-15 (hetIL-15) treatment on uninfected rhesus macaques and on macaques that had spontaneously controlled SHIV infection to low levels of chronic viremia. hetIL-15 increased effector CD8(+) T lymphocytes with high granzyme B content in blood, mucosal sites and lymph nodes, including virus-specific MHC-peptide tetramer+ CD8(+) cells in LN. Following hetIL-15 treatment, multiplexed quantitative image analysis (histo-cytometry) of LN revealed increased numbers of granzyme B(+) T cells in B cell follicles and SHIV RNA was decreased in plasma and in LN. Based on these properties, hetIL-15 shows promise as a potential component in combination immunotherapy regimens to target AIDS virus sanctuaries and reduce long-term viral reservoirs in HIV-1 infected individuals. Trial registration: ClinicalTrials.gov NCT02452268 Public Library of Science 2018-02-23 /pmc/articles/PMC5825155/ /pubmed/29474450 http://dx.doi.org/10.1371/journal.ppat.1006902 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Watson, Dionysios C. Moysi, Eirini Valentin, Antonio Bergamaschi, Cristina Devasundaram, Santhi Fortis, Sotirios P. Bear, Jenifer Chertova, Elena Bess, Julian Sowder, Ray Venzon, David J. Deleage, Claire Estes, Jacob D. Lifson, Jeffrey D. Petrovas, Constantinos Felber, Barbara K. Pavlakis, George N. Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title | Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title_full | Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title_fullStr | Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title_full_unstemmed | Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title_short | Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes |
title_sort | treatment with native heterodimeric il-15 increases cytotoxic lymphocytes and reduces shiv rna in lymph nodes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5825155/ https://www.ncbi.nlm.nih.gov/pubmed/29474450 http://dx.doi.org/10.1371/journal.ppat.1006902 |
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