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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 6

Killing of target cells.

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Killing of target cells.
Intravital 2-photon microscopy in the bone marr...
Intravital 2-photon microscopy in the bone marrow: Killing was determined in FV-infected, CTL-transferred C57BL/6 or DEREG mice (for Treg depletion) at 8, 10, and 14 dpi with and without Treg depletion. Target cell death was assessed based on fading of fluorescence and loss of clear cell structure. (A) Representative killing event caused by multiple CTL contacts 10 dpi in a time series. Contact was assessed based on a distance of less than 3 μm between an FV-specific tdTom+ CTL and target and highlighted by green surrounding the contacting CTL. The contact duration is indicated by the length of the track. Red: FV-specific tdTom+ CTLs. Green: target cells. Blue: control cells. Yellow track: CTL track while in contact with target cell. Scale bars: 100 μm (overview image) and 20 μm (zoomed-in images). For the full movie, see Supplemental Video 5. (B) Number of target cells over imaging time. Target count was evaluated at the beginning and at 1 and 2 hours of imaging. Data represent the median ± IQR of 6 individual mice per group. (C) Expression of cytotoxicity-associated molecules. Flow cytometry was used to identify the intracellular expression of GZMB, GZMA, and IFN-γ and the surface expression of CD107a on activated CD43+ CTLs in FV-infected mice 10 dpi and 14 dpi with and without Treg depletion. Radar chart represents the mean number of GZMB+, GZMA+, IFN-γ+, or CD107+CD43+ CTLs per million. The mean value was calculated from 1 experiment with 4 mice per group.

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