Regulatory CD4+and CD8+T cells are negatively correlated with CD4+/CD8+T cell ratios in patients acutely infected with SARS-CoV-2
Regulatory CD4+and CD8+T cells are negatively correlated with CD4+/CD8+T cell ratios in patients acutely infected with SARS-CoV-2
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DOI:
10.1002/jlb.5cova0720-421rr
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发表时间:
2020-09-15
影响因子:
5.5
通讯作者:
Zhu, Zhaoqin
中科院分区:
文献类型:
--
作者:
Gao, Menglu;Liu, Yili;Zhu, Zhaoqin
Regulatory T cell can protect against severe forms of coronaviral infections attributable to host inflammatory responses. But its role in the pathogenesis of COVID-19 is still unclear. In this study, frequencies of total and multiple subsets of lymphocytes in peripheral blood of COVID-19 patients and discharged individuals were analyzed using a multicolor flow cytometry assay. Plasma concentration of IL-10 was measured using a microsphere-based immunoassay kit. Comparing to healthy controls, the frequencies of total lymphocytes and T cells decreased significantly in both acutely infected COVID-19 patients and discharged individuals. The frequencies of total lymphocytes correlated negatively with the frequencies of CD3(-)CD56(+)NK cells. The frequencies of regulatory CD8(+)CD25(+)T cells correlated with CD4(+)/CD8(+)T cell ratios positively, while the frequencies of regulatory CD4(+)CD25(+)CD127(-)T cells correlated negatively with CD4(+)/CD8(+)T cell ratios. Ratios of CD4(+)/CD8(+)T cells increased significantly in patients beyond age of 45 years. And accordingly, the frequencies of regulatory CD8(+)CD25(+)T cells were also found significantly increased in these patients. Collectively, the results suggest that regulatory CD4(+)and CD8(+)T cells may play distinct roles in the pathogenesis of COVID-19. Moreover, the data indicate that NK cells might contribute to the COVID-19 associated lymphopenia.