Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mittermüller, Daniela, Otto, Lucas, Long, Zoë, Kraus, Andreas, Beer, Alexander, Hasenberg, Anja, Zelinskyy, Gennadiy, Westmeier, Jaana, Hasenkrug, Kim J., Dittmer, Ulf, Gunzer, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
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
_version_ 1785078125402521600
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
work_keys_str_mv AT mittermullerdaniela regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT ottolucas regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT longzoe regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT krausandreas regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT beeralexander regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT hasenberganja regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT zelinskyygennadiy regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT westmeierjaana regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT hasenkrugkimj regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT dittmerulf regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice
AT gunzermatthias regulatorytcellssuppressthemotilityofcytotoxictcellsinfriendretrovirusinfectedmice