COVID-19: imbalanced cell-mediated immune response drives to immunopathology

被引:20
|
作者
Wang, Jun [1 ,2 ,3 ]
Li, Qian [1 ,2 ]
Qiu, YuanWang [3 ,4 ]
Lu, Hongzhou [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Peoples Hosp 3, Natl Clin Res Ctr Infect Dis, Dept Infect Dis, Shenzhen, Peoples R China
[2] Southern Univ Sci & Technol, Affiliated Hosp 2, Shenzhen, Peoples R China
[3] Jiangnan Univ, Peoples Hosp Wuxi 5, Clin Lab, Wuxi, Jiangsu, Peoples R China
[4] Jiangnan Univ, Peoples Hosp Wuxi 5, Dept Hepatol, 1314 Guangrui Rd, Wuxi 215006, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
COVID-19; SARS-CoV-2; NETs; pathogenesis; cytokine storm; III INTERFERONS; CYTOKINE STORM; CORONAVIRUS; INDUCTION;
D O I
10.1080/22221751.2022.2122579
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), poses an imminent threat to humanity. SARS-CoV-2 invades host cells, causing a failure of host immune recognition. Instead of an effective antiviral immunological response after SARS-CoV-2 invasion, the cascading pathological syndrome of COVID-19, especially in severe disease, is exacerbated by an overt inflammatory response and the suppression of SARS-CoV-2-specific immune responses. As is known, excessive inflammation leads to pathophysiological changes in virus-infected tissues or organs, manifested by imbalanced immune responses, cytokine storm, and aggressive neutrophil activation, ultimately leading to lung damage, such as alveolar damage, endotheliitis, and fluid overload. However, the triggers and consequences of a disruption to immune system homeostasis and the underlying mechanisms of uncontrolled immunopathology following viral infection remain unclear. Here, we review the dynamic and systemic immune progression from an imbalance in cell-mediated immune responses to COVID-19 lung injury. Our understanding of key mechanisms involved in pathogenesis is critical for the development of therapeutic agents and to optimize therapeutic strategies.
引用
收藏
页码:2393 / 2404
页数:12
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