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Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection
Cytomegalovirus-based vaccine vectors offer interesting opportunities for T cell-based vaccination purposes as CMV infection induces large numbers of functional effector-like cells that accumulate in peripheral tissues, a process termed memory inflation. Maintenance of high numbers of peripheral CD8...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211020/ https://www.ncbi.nlm.nih.gov/pubmed/32385253 http://dx.doi.org/10.1038/s41467-020-16219-3 |
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author | Welten, Suzanne P. M. Yermanos, Alexander Baumann, Nicolas S. Wagen, Franziska Oetiker, Nathalie Sandu, Ioana Pedrioli, Alessandro Oduro, Jennifer D. Reddy, Sai T. Cicin-Sain, Luka Held, Werner Oxenius, Annette |
author_facet | Welten, Suzanne P. M. Yermanos, Alexander Baumann, Nicolas S. Wagen, Franziska Oetiker, Nathalie Sandu, Ioana Pedrioli, Alessandro Oduro, Jennifer D. Reddy, Sai T. Cicin-Sain, Luka Held, Werner Oxenius, Annette |
author_sort | Welten, Suzanne P. M. |
collection | PubMed |
description | Cytomegalovirus-based vaccine vectors offer interesting opportunities for T cell-based vaccination purposes as CMV infection induces large numbers of functional effector-like cells that accumulate in peripheral tissues, a process termed memory inflation. Maintenance of high numbers of peripheral CD8 T cells requires continuous replenishment of the inflationary T cell pool. Here, we show that the inflationary T cell population contains a small subset of cells expressing the transcription factor Tcf1. These Tcf1(+) cells resemble central memory T cells and are proliferation competent. Upon sensing viral reactivation events, Tcf1(+) cells feed into the pool of peripheral Tcf1(−) cells and depletion of Tcf1(+) cells hampers memory inflation. TCR repertoires of Tcf1(+) and Tcf1(−) populations largely overlap, with the Tcf1(+) population showing higher clonal diversity. These data show that Tcf1(+) cells are necessary for sustaining the inflationary T cell response, and upholding this subset is likely critical for the success of CMV-based vaccination approaches. |
format | Online Article Text |
id | pubmed-7211020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72110202020-05-13 Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection Welten, Suzanne P. M. Yermanos, Alexander Baumann, Nicolas S. Wagen, Franziska Oetiker, Nathalie Sandu, Ioana Pedrioli, Alessandro Oduro, Jennifer D. Reddy, Sai T. Cicin-Sain, Luka Held, Werner Oxenius, Annette Nat Commun Article Cytomegalovirus-based vaccine vectors offer interesting opportunities for T cell-based vaccination purposes as CMV infection induces large numbers of functional effector-like cells that accumulate in peripheral tissues, a process termed memory inflation. Maintenance of high numbers of peripheral CD8 T cells requires continuous replenishment of the inflationary T cell pool. Here, we show that the inflationary T cell population contains a small subset of cells expressing the transcription factor Tcf1. These Tcf1(+) cells resemble central memory T cells and are proliferation competent. Upon sensing viral reactivation events, Tcf1(+) cells feed into the pool of peripheral Tcf1(−) cells and depletion of Tcf1(+) cells hampers memory inflation. TCR repertoires of Tcf1(+) and Tcf1(−) populations largely overlap, with the Tcf1(+) population showing higher clonal diversity. These data show that Tcf1(+) cells are necessary for sustaining the inflationary T cell response, and upholding this subset is likely critical for the success of CMV-based vaccination approaches. Nature Publishing Group UK 2020-05-08 /pmc/articles/PMC7211020/ /pubmed/32385253 http://dx.doi.org/10.1038/s41467-020-16219-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Welten, Suzanne P. M. Yermanos, Alexander Baumann, Nicolas S. Wagen, Franziska Oetiker, Nathalie Sandu, Ioana Pedrioli, Alessandro Oduro, Jennifer D. Reddy, Sai T. Cicin-Sain, Luka Held, Werner Oxenius, Annette Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title | Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title_full | Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title_fullStr | Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title_full_unstemmed | Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title_short | Tcf1(+) cells are required to maintain the inflationary T cell pool upon MCMV infection |
title_sort | tcf1(+) cells are required to maintain the inflationary t cell pool upon mcmv infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211020/ https://www.ncbi.nlm.nih.gov/pubmed/32385253 http://dx.doi.org/10.1038/s41467-020-16219-3 |
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