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Mechanisms of mast cells and T cells interaction during viral infections

Subject Area Dermatology
Immunology
Term from 2016 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 322360721
 
Final Report Year 2021

Final Report Abstract

We investigated the role of MCs in the development of virus-specific CD8+ T cell responses using the well-characterized murine lymphocytic choriomeningitis virus (LCMV) model and the transgenic MasTRECK mice that contain the human diphtheria toxin receptor as an inducible MC-deficient model. Here, we report that MCs are essential for the activation and expansion of virus-specific CD8+ T cells. After MC depletion and subsequent LCMV infection, the CD8+ T cell effector phenotype and antiviral cytokine production were impaired at the peak of infection. Importantly, MC-deficient mice were unable to control the infection and exhibited significantly higher viral loads in the spleen and draining lymph nodes compared to that of wild type control mice. In the absence of MCs, dendritic cell (DC) activation was impaired upon LCMV infection and type-I interferon levels were reduced during the first days of infection. In summary, our results indicate that MCs play a pivotal role in the activation and antiviral functions of CD8+ T cells through proper DC activation. In addition, we can also report that Th2-polarized T cells lacking the transcription factor T-bet harbor strong immunomodulatory potential and suppress antigen-specific CD8+ T cells via IL-10.

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