| Literature DB >> 34193870 |
Jae Hyung Jung1, Min-Seok Rha1,2, Moa Sa1,3, Hee Kyoung Choi4, Ji Hoon Jeon4, Hyeri Seok4, Dae Won Park4, Su-Hyung Park1,3, Hye Won Jeong5, Won Suk Choi6, Eui-Cheol Shin7,8.
Abstract
Memory T cells contribute to rapid viral clearance during re-infection, but the longevity and differentiation of SARS-CoV-2-specific memory T cells remain unclear. Here we conduct ex vivo assays to evaluate SARS-CoV-2-specific CD4+ and CD8+ T cell responses in COVID-19 convalescent patients up to 317 days post-symptom onset (DPSO), and find that memory T cell responses are maintained during the study period regardless of the severity of COVID-19. In particular, we observe sustained polyfunctionality and proliferation capacity of SARS-CoV-2-specific T cells. Among SARS-CoV-2-specific CD4+ and CD8+ T cells detected by activation-induced markers, the proportion of stem cell-like memory T (TSCM) cells is increased, peaking at approximately 120 DPSO. Development of TSCM cells is confirmed by SARS-CoV-2-specific MHC-I multimer staining. Considering the self-renewal capacity and multipotency of TSCM cells, our data suggest that SARS-CoV-2-specific T cells are long-lasting after recovery from COVID-19, thus support the feasibility of effective vaccination programs as a measure for COVID-19 control.Entities:
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Year: 2021 PMID: 34193870 DOI: 10.1038/s41467-021-24377-1
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919