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Regulatory T cells suppress the motility of cytotoxic T cells in Friend retrovirus–infected mice
Daniela Mittermüller, Lucas Otto, Zoë Long, Andreas Kraus, Alexander Beer, Anja Hasenberg, Gennadiy Zelinskyy, Jaana Westmeier, Kim J. Hasenkrug, Ulf Dittmer, Matthias Gunzer
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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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 5

Contact with CTL targets.

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Contact with CTL targets.
Intravital 2-photon microscopy in the bone mar...
Intravital 2-photon microscopy in the bone marrow: FV-infected, CTL-transferred C57BL/6 or DEREG mice (for Treg depletion) were inoculated with a 1:1 mix of target and control cells 5 minutes before bone marrow imaging. Contact with target or control cells was assessed based on a distance of less than 3 μm. Contact duration was determined through automated CTL track generation from the moment of contact until contact disruption. (A) Representative contact between CTLs and targets 10 dpi and 14 dpi. Contact with target at 10 dpi is shown in a time series. Contact is indicated by green surrounding a CTL, and no contact by red surrounding a CTL. Red: FV-specific tdTom+ CTL. Green: target cell. Blue: control cell. Yellow track: CTL track without target cell contact. Blue track: CTL track with target cell contact. Scale bars: 50 μm. For full movies, see Supplemental Video 3 (10 dpi) and Supplemental Video 4 (14 dpi). (B) Contact duration of CTLs and target cells, in minutes. (C) Contact duration of CTLs and unloaded control cells, in minutes. (D) Comparison of CTL contact duration between contact with targets and control cells as shown in panels A and B. Data represent the values of individual cells in 3 individual mice per group (median ± IQR). P values were obtained by Kruskal-Wallis test followed by Dunn’s multiple-comparison test. *P < 0.05.

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