Innate immune and inflammatory responses to SARS-CoV-2: Implications for COVID-19

被引:174
|
作者
Lowery, Shea A. [1 ]
Sariol, Alan [2 ]
Perlman, Stanley [1 ,2 ]
机构
[1] Univ Iowa, Dept Microbiol & Immunol, Iowa City, IA 52242 USA
[2] Univ Iowa, Interdisciplinary Program Immunol, Iowa City, IA 52242 USA
关键词
MOUSE HEPATITIS-VIRUS; I INTERFERON; INFECTED MACROPHAGES; PNEUMONIA; INDUCTION;
D O I
10.1016/j.chom.2021.05.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
COVID-19 can result in severe disease characterized by significant immunopathology that is spurred by an exuberant, yet dysregulated, innate immune response with a poor adaptive response. A limited and delayed interferon I (IFN-I) and IFN-III response results in exacerbated proinflammatory cytokine production and in extensive cellular infiltrates in the respiratory tract, resulting in lung pathology. The development of effective therapeutics for patients with severe COVID-19 depends on our understanding of the pathological elements of this unbalanced innate immune response. Here, we review the mechanisms by which SARS-CoV-2 both activates and antagonizes the IFN and inflammatory response following infection, how a dysregulated cytokine and cellular response contributes to immune-mediated pathology in COVID-19, and therapeutic strategies that target elements of the innate response.
引用
收藏
页码:1052 / 1062
页数:11
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