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10.1038/s41467-021-24377-1

http://scihub22266oqcxt.onion/10.1038/s41467-021-24377-1
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suck abstract from ncbi


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pmid34193870      Nat+Commun 2021 ; 12 (1): 4043
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  • SARS-CoV-2-specific T cell memory is sustained in COVID-19 convalescent patients for 10 months with successful development of stem cell-like memory T cells #MMPMID34193870
  • Jung JH; Rha MS; Sa M; Choi HK; Jeon JH; Seok H; Park DW; Park SH; Jeong HW; Choi WS; Shin EC
  • Nat Commun 2021[Jun]; 12 (1): 4043 PMID34193870show ga
  • 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 (T(SCM)) cells is increased, peaking at approximately 120 DPSO. Development of T(SCM) cells is confirmed by SARS-CoV-2-specific MHC-I multimer staining. Considering the self-renewal capacity and multipotency of T(SCM) 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.
  • |Antibodies, Viral/blood[MESH]
  • |CD4-Positive T-Lymphocytes/*immunology[MESH]
  • |CD8-Positive T-Lymphocytes/*immunology[MESH]
  • |COVID-19 Vaccines/immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Humans[MESH]
  • |Immunologic Memory/*immunology[MESH]
  • |Interferon-gamma/blood[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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