Initial COVID-19 severity influenced by SARS-CoV-2-specific T cells imprints T-cell memory and inversely affects reinfection

SARS-CoV-2特异性T细胞会影响COVID-19的初始严重程度,从而影响T细胞记忆,并反过来影响再次感染。

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作者:Gang Yang #,Jinpeng Cao #,Jian Qin #,Xinyue Mei #,Shidong Deng,Yingjiao Xia,Jun Zhao,Junxiang Wang,Tao Luan,Daxiang Chen,Peiyu Huang,Cheng Chen,Xi Sun,Qi Luo,Jie Su,Yunhui Zhang,Nanshan Zhong ,Zhongfang Wang

Abstract

The immunoprotective components control COVID-19 disease severity, as well as long-term adaptive immunity maintenance and subsequent reinfection risk discrepancies across initial COVID-19 severity, remain unclarified. Here, we longitudinally analyzed SARS-CoV-2-specific immune effectors during the acute infection and convalescent phases of 165 patients with COVID-19 categorized by severity. We found that early and robust SARS-CoV-2-specific CD4+ and CD8+ T cell responses ameliorate disease progression and shortened hospital stay, while delayed and attenuated virus-specific CD8+ T cell responses are prominent severe COVID-19 features. Delayed antiviral antibody generation rather than titer level associates with severe outcomes. Conversely, initial COVID-19 severity imprints the long-term maintenance of SARS-CoV-2-specific adaptive immunity, demonstrating that severe convalescents exhibited more sustained virus-specific antibodies and memory T cell responses compared to mild/moderate counterparts. Moreover, initial COVID-19 severity inversely correlates with SARS-CoV-2 reinfection risk. Overall, our study unravels the complicated interaction between temporal characteristics of virus-specific T cell responses and COVID-19 severity to guide future SARS-CoV-2 wave management.

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