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HTNV infection induces activation and deficiency of CD8 +MAIT cells in HFRS patients.

Yu-Si ZhangMeng WangXiyue ZhangKang TangChunmei ZhangXiaozhou JiaHaifeng HuHe LiuNa LiRan ZhuangBoquan JinYing MaYun Zhang
Published in: Clinical and experimental immunology (2022)
Hantaan virus (HTNV) infection causes an epidemic of hemorrhagic fever with renal syndrome (HFRS) mainly in Asia. Mucosal-associated invariant T (MAIT) cells are innate-like T lymphocytes known to play an important role in innate host defense during virus infection. However, their roles and phenotypes during HTNV infection have not yet been explored. We characterized CD8 +MAIT cells from HFRS patients based on scRNA-seq data combined with flow cytometry data. We showed that HTNV infection caused the loss and activation of CD8 +MAIT cells in the peripheral blood, which were correlated with disease severity. The production of granzyme B and IFN-γ from CD8 +MAIT cells and the limitation of HTNV replication in endothelia cells indicated the anti-viral property of CD8 +MAIT cells. In addition, in vitro infection of MAIT cells by HTNV or HTNV-exposed monocytes showed that the activation of MAIT cells was IL-18-mediated. In conclusion, this study identified, for the first time, gene expression profiles of MAIT cells, provided underlying molecular mechanisms for activation of MAIT cells during HTNV infection, and suggested a potential anti-viral role of MAIT cells in HFRS.
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