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宿主细胞固有先天免疫识别 SARS-CoV-2。

Host cell-intrinsic innate immune recognition of SARS-CoV-2.

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 631100, USA; Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA; The Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Curr Opin Virol. 2022 Feb;52:30-38. doi: 10.1016/j.coviro.2021.11.002. Epub 2021 Nov 11.

Abstract

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) emerged at the end of 2019 and caused the pandemic of coronavirus disease 2019 (COVID-19). Basic and clinical investigations indicate that severe forms of COVID-19 are due in part to dysregulated immune responses to virus infection. The innate immune system is the first line of host defense against most virus infections, with pathogen recognition receptors detecting SARS-CoV-2 RNA and protein components and initiating pro-inflammatory and antiviral responses. Notwithstanding this response, SARS-CoV-2 proteins evade, inhibit, and skew innate immune signaling early in infection. In this review, we highlight the components of cell-based recognition of SARS-CoV-2 infection and the mechanisms employed by the virus to modulate these innate immune host defense pathways.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)于 2019 年末出现,引发了 2019 年冠状病毒病(COVID-19)大流行。基础和临床研究表明,COVID-19 的严重形式部分是由于对病毒感染的免疫反应失调。先天免疫系统是宿主抵御大多数病毒感染的第一道防线,病原体识别受体检测 SARS-CoV-2 RNA 和蛋白成分,并启动促炎和抗病毒反应。尽管有这种反应,SARS-CoV-2 蛋白在感染早期逃避、抑制和扭曲先天免疫信号。在这篇综述中,我们强调了细胞识别 SARS-CoV-2 感染的组成部分,以及病毒用来调节这些先天免疫宿主防御途径的机制。

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