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10.1016/j.xcrm.2020.100081

http://scihub22266oqcxt.onion/10.1016/j.xcrm.2020.100081
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suck abstract from ncbi


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pmid32839763      Cell+Rep+Med 2020 ; 1 (6): 100081
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  • SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential #MMPMID32839763
  • Neidleman J; Luo X; Frouard J; Xie G; Gill G; Stein ES; McGregor M; Ma T; George AF; Kosters A; Greene WC; Vasquez J; Ghosn E; Lee S; Roan NR
  • Cell Rep Med 2020[Sep]; 1 (6): 100081 PMID32839763show ga
  • Convalescing coronavirus disease 2019 (COVID-19) patients mount robust T cell responses against SARS-CoV-2, suggesting an important role of T cells in viral clearance. To date, the phenotypes of SARS-CoV-2-specific T cells remain poorly defined. Using 38-parameter CyTOF, we phenotyped longitudinal specimens of SARS-CoV-2-specific CD4+ and CD8+ T cells from nine individuals who recovered from mild COVID-19. SARS-CoV-2-specific CD4+ T cells were exclusively Th1 cells and predominantly Tcm cells with phenotypic features of robust helper function. SARS-CoV-2-specific CD8+ T cells were predominantly Temra cells in a state of less terminal differentiation than most Temra cells. Subsets of SARS-CoV-2-specific T cells express CD127, can proliferate homeostatically, and can persist for over 2 months. Our results suggest that long-lived and robust T cell immunity is generated following natural SARS-CoV-2 infection and support an important role of SARS-CoV-2-specific T cells in host control of COVID-19.
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