MHC Class I Molecules Exacerbate Viral Infection by Disrupting Type I Interferon Signaling

被引:18
作者
Xia, Simo [1 ]
Tao, Yijie [1 ]
Cui, Likun [1 ]
Yu, Yizhi [1 ]
Xu, Sheng [1 ]
机构
[1] Second Mil Med Univ, Inst Immunol, Natl Key Lab Med Immunol, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
CELLS; TRANSDUCTION; BETA(2)-MICROGLOBULIN; RECEPTORS;
D O I
10.1155/2019/5370706
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MHC class I molecules are key in the presentation of antigen and initiation of adaptive CD8+ T cell responses. In addition to its classical activity, MHC I may possess nonclassical functions. We have previously identified a regulatory role of MHC I in TLR signaling and antibacterial immunity. However, its role in innate antiviral immunity remains unknown. In this study, we found a reduced viral load in MHC I-deficient macrophages that was independent of type I IFN production. Mechanically, MHC I mediated viral suppression by inhibiting the type I IFN signaling pathway, which depends on SHP2. Cross-linking MHC I at the membrane increased SHP2 activation and further suppressed STAT1 phosphorylation. Therefore, our data revealed an inhibitory role of MHC I in type I IFN response to viral infection and expanded our understanding of MHC I and antigen presentation.
引用
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页数:9
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