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Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice
Daniela Mittermüller, … , Ulf Dittmer, Matthias Gunzer
Daniela Mittermüller, … , Ulf Dittmer, Matthias Gunzer
Published July 10, 2023
Citation Information: JCI Insight. 2023;8(13):e167482. https://doi.org/10.1172/jci.insight.167482.
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Research Article Immunology Virology

Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice

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Abstract

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.

Authors

Daniela Mittermüller, Lucas Otto, Zoë Long, Andreas Kraus, Alexander Beer, Anja Hasenberg, Gennadiy Zelinskyy, Jaana Westmeier, Kim J. Hasenkrug, Ulf Dittmer, Matthias Gunzer

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Figure 1

Evaluation of CTL motility through intravital 2-photon imaging.

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Evaluation of CTL motility through intravital 2-photon imaging.
(A and B...
(A and B) Schematic representation of the experimental design of the intravital 2-photon bone marrow imaging. (A) C57BL/6 or DEREG acceptor mice were infected with FV followed by the transfer of 1000 FV-specific tdTom+ CTLs, obtained by blood draw from TCR-Lck-tdTom donor mice. Intravital 2-photon bone marrow imaging was performed on 8, 10, and 14 dpi. For visualization or additional depletion of Tregs, DEREG mice were used as acceptor mice and treated with diphtheria toxin or left untreated. (B) For evaluation of contacts with potential targets, a mix of target and control cells prepared from B cells isolated from the spleens of donor mice were transferred to FV-infected, CTL-transferred C57BL/6 or DEREG (Treg depletion) recipient mice directly before imaging at 8, 10, and 14 dpi. Tregs were depleted in FV-infected, CTL-transferred DEREG mice for visualization 14 dpi in the absence of Tregs. (C) Image of a mouse that underwent surgery for intravital bone marrow imaging and exemplary picture of the bone marrow obtained by intravital 2-photon microscopy. Red: FV-specific tdTom+ CTLs. Blue: blood flow was visualized using QT655. Green: EGFP+ Tregs. (D) Representative tibial image obtained from FV-mWasabi–infected CTL-transferred mouse 8 dpi in intravital 2-photon microscopy (yellow: FV-infected cells; red: FV-specific tdTom+ CTLs). Scale bars: 100 μm.

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