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10.1016/j.bbrc.2020.10.060

http://scihub22266oqcxt.onion/10.1016/j.bbrc.2020.10.060
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33190827!7584424!33190827
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suck abstract from ncbi


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pmid33190827      Biochem+Biophys+Res+Commun 2021 ; 538 (ä): 211-217
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  • T cell immunity to SARS-CoV-2 following natural infection and vaccination #MMPMID33190827
  • DiPiazza AT; Graham BS; Ruckwardt TJ
  • Biochem Biophys Res Commun 2021[Jan]; 538 (ä): 211-217 PMID33190827show ga
  • SARS-CoV-2 first emerged in the human population in late 2019 in Wuhan, China, and in a matter of months, spread across the globe resulting in the Coronavirus Disease 19 (COVID-19) pandemic and substantial economic fallout. SARS-CoV-2 is transmitted between humans via respiratory particles, with infection presenting a spectrum of clinical manifestations ranging from asymptomatic to respiratory failure with multiorgan dysfunction and death in severe cases. Prior experiences with human pathogenic coronaviruses and respiratory virus diseases in general have revealed an important role for cellular immunity in limiting disease severity. Here, we review some of the key mechanisms underlying cell-mediated immunity to respiratory viruses and summarize our current understanding of the functional capacity and role of SARS-CoV-2-specific T cells following natural infection and vaccination.
  • |COVID-19 Vaccines/immunology/*therapeutic use[MESH]
  • |COVID-19/*immunology/*prevention & control[MESH]
  • |Humans[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |T-Lymphocytes/*immunology[MESH]


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