登革热病毒
免疫学
丙型肝炎病毒
干扰素
生物
T细胞受体
病毒
细胞因子
体内
病毒学
病毒复制
登革热
T细胞
免疫系统
生物技术
作者
Bonnie van Wilgenburg,Iris Scherwitzl,Edward C. Hutchinson,Tianqi Leng,Ayako Kurioka,Corinna A. Kulicke,Catherine de Lara,Suzanne Cole,Sirijitt Vasanawathana,Wannee Limpitikul,Prida Malasit,Duncan Young,Laura Denney,Eleanor J. Barnes,Jonathan K. Ball,Gary Burgess,Graham Cooke,John Francis Dillon,Charles Gore,Graham R. Foster
摘要
Mucosal-associated invariant T (MAIT) cells are abundant in humans and recognize bacterial ligands. Here, we demonstrate that MAIT cells are also activated during human viral infections in vivo. MAIT cells activation was observed during infection with dengue virus, hepatitis C virus and influenza virus. This activation-driving cytokine release and Granzyme B upregulation-is TCR-independent but dependent on IL-18 in synergy with IL-12, IL-15 and/or interferon-α/β. IL-18 levels and MAIT cell activation correlate with disease severity in acute dengue infection. Furthermore, HCV treatment with interferon-α leads to specific MAIT cell activation in vivo in parallel with an enhanced therapeutic response. Moreover, TCR-independent activation of MAIT cells leads to a reduction of HCV replication in vitro mediated by IFN-γ. Together these data demonstrate MAIT cells are activated following viral infections, and suggest a potential role in both host defence and immunopathology.
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