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Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice
Antiviral immunity often requires CD8(+) cytotoxic T lymphocytes (CTLs) that actively migrate and search for virus-infected targets. Regulatory T cells (Tregs) have been shown to suppress CTL responses, but it is not known whether this is also mediated by effects on CTL motility. Here, we used intra...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371334/ https://www.ncbi.nlm.nih.gov/pubmed/37427590 http://dx.doi.org/10.1172/jci.insight.167482 |
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author | Mittermüller, Daniela Otto, Lucas Long, Zoë Kraus, Andreas Beer, Alexander Hasenberg, Anja Zelinskyy, Gennadiy Westmeier, Jaana Hasenkrug, Kim J. Dittmer, Ulf Gunzer, Matthias |
author_facet | Mittermüller, Daniela Otto, Lucas Long, Zoë Kraus, Andreas Beer, Alexander Hasenberg, Anja Zelinskyy, Gennadiy Westmeier, Jaana Hasenkrug, Kim J. Dittmer, Ulf Gunzer, Matthias |
author_sort | Mittermüller, Daniela |
collection | PubMed |
description | Antiviral immunity often requires CD8(+) cytotoxic T lymphocytes (CTLs) that actively migrate and search for virus-infected targets. Regulatory T cells (Tregs) have been shown to suppress CTL responses, but it is not known whether this is also mediated by effects on CTL motility. Here, we used intravital 2-photon microscopy in the Friend retrovirus (FV) mouse model to define the impact of Tregs on CTL motility throughout the course of acute infection. Virus-specific CTLs were very motile and had frequent short contacts with target cells at their peak cytotoxic activity. However, when Tregs were activated and expanded in late-acute FV infection, CTLs became significantly less motile and contacts with target cells were prolonged. This phenotype was associated with development of functional CTL exhaustion. Tregs had direct contacts with CTLs in vivo and, importantly, their experimental depletion restored CTL motility. Our findings identify an effect of Tregs on CTL motility as part of their mechanism of functional impairment in chronic viral infections. Future studies must address the underlying molecular mechanisms. |
format | Online Article Text |
id | pubmed-10371334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-103713342023-07-27 Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice Mittermüller, Daniela Otto, Lucas Long, Zoë Kraus, Andreas Beer, Alexander Hasenberg, Anja Zelinskyy, Gennadiy Westmeier, Jaana Hasenkrug, Kim J. Dittmer, Ulf Gunzer, Matthias JCI Insight Research Article Antiviral immunity often requires CD8(+) cytotoxic T lymphocytes (CTLs) that actively migrate and search for virus-infected targets. Regulatory T cells (Tregs) have been shown to suppress CTL responses, but it is not known whether this is also mediated by effects on CTL motility. Here, we used intravital 2-photon microscopy in the Friend retrovirus (FV) mouse model to define the impact of Tregs on CTL motility throughout the course of acute infection. Virus-specific CTLs were very motile and had frequent short contacts with target cells at their peak cytotoxic activity. However, when Tregs were activated and expanded in late-acute FV infection, CTLs became significantly less motile and contacts with target cells were prolonged. This phenotype was associated with development of functional CTL exhaustion. Tregs had direct contacts with CTLs in vivo and, importantly, their experimental depletion restored CTL motility. Our findings identify an effect of Tregs on CTL motility as part of their mechanism of functional impairment in chronic viral infections. Future studies must address the underlying molecular mechanisms. American Society for Clinical Investigation 2023-07-10 /pmc/articles/PMC10371334/ /pubmed/37427590 http://dx.doi.org/10.1172/jci.insight.167482 Text en © 2023 Mittermüller et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Mittermüller, Daniela Otto, Lucas Long, Zoë Kraus, Andreas Beer, Alexander Hasenberg, Anja Zelinskyy, Gennadiy Westmeier, Jaana Hasenkrug, Kim J. Dittmer, Ulf Gunzer, Matthias Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title | Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title_full | Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title_fullStr | Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title_full_unstemmed | Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title_short | Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice |
title_sort | regulatory t cells suppress the motility of cytotoxic t cells in friend retrovirus–infected mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371334/ https://www.ncbi.nlm.nih.gov/pubmed/37427590 http://dx.doi.org/10.1172/jci.insight.167482 |
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