| Literature DB >> 33603759 |
Ling Ni1,2, Meng-Li Cheng3,4, Yu Feng1, Hui Zhao4, Jingyuan Liu5, Fang Ye6, Qing Ye4, Gengzhen Zhu1, Xiaoli Li1, Pengzhi Wang1, Jing Shao1, Yong-Qiang Deng4, Peng Wei1, Fang Chen7, Cheng-Feng Qin4, Guoqing Wang3, Fan Li3,8, Hui Zeng5, Chen Dong1,2,9.
Abstract
The high infection rate and rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) make it a world-wide pandemic. Individuals infected by the virus exhibited different degrees of symptoms, and most convalescent individuals have been shown to develop both cellular and humoral immune responses. However, virus-specific adaptive immune responses in severe patients during acute phase have not been thoroughly studied. Here, we found that in a group of COVID-19 patients with acute respiratory distress syndrome (ARDS) during hospitalization, most of them mounted SARS-CoV-2-specific antibody responses, including neutralizing antibodies. However, compared to healthy controls, the percentages and absolute numbers of both NK cells and CD8+ T cells were significantly reduced, with decreased IFNγ expression in CD4+ T cells in peripheral blood from severe patients. Most notably, their peripheral blood lymphocytes failed in producing IFNγ against viral proteins. Thus, severe COVID-19 patients at acute infection stage developed SARS-CoV-2-specific antibody responses but were impaired in cellular immunity, which emphasizes on the role of cellular immunity in COVID-19.Entities:
Keywords: SARS-CoV-2; T cells; acute respiratory distress syndrome; adaptive immunity; interferon gamma; neutralization antibody
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Year: 2021 PMID: 33603759 PMCID: PMC7884325 DOI: 10.3389/fimmu.2021.603563
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561