Immune evasion of SARS-CoV-2 from interferon antiviral system

被引:45
作者
Min, Yuan-Qin [1 ,2 ]
Huang, Mengzhuo [1 ,3 ]
Sun, Xiulian [1 ,2 ]
Deng, Fei [1 ,2 ]
Wang, Hualin [1 ,2 ]
Ning, Yun-Jia [1 ,2 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
[2] Chinese Acad Sci, Ctr Biosafety Megasci, Wuhan 430071, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 101408, Peoples R China
基金
中国国家自然科学基金;
关键词
SARS-CoV-2; COVID-19; Coronavirus; Interferon; Immune evasion; Innate immunity; PAPAIN-LIKE PROTEASE; HOST GENE-EXPRESSION; CYCLIC GMP-AMP; I INTERFERON; NONSTRUCTURAL PROTEIN-1; III INTERFERONS; CORONAVIRUS; INNATE; INDUCTION; IRF3;
D O I
10.1016/j.csbj.2021.07.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The on-going pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has led to unprecedented medical and socioeconomic crises. Although the viral pathogenesis remains elusive, deficiency of effective antiviral interferon (IFN) responses upon SARS-CoV-2 infection has been recognized as a hallmark of COVID-19 contributing to the disease pathology and progress. Recently, multiple proteins encoded by SARS-CoV-2 have been shown to act as potential IFN antagonists with diverse possible mechanisms. Here, we summarize and discuss the strategies of SARS-CoV-2 for evasion of innate immunity (particularly the antiviral IFN responses), understanding of which will facilitate not only the elucidation of SARS-CoV-2 infection and pathogenesis but also the development of antiviral intervention therapies. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:4217 / 4225
页数:9
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