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10.1016/j.cell.2020.05.015

http://scihub22266oqcxt.onion/10.1016/j.cell.2020.05.015
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C7237901!7237901!32473127
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suck abstract from ncbi


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pmid32473127      Cell 2020 ; 181 (7): 1489-1501.e15
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  • Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals #MMPMID32473127
  • Grifoni A; Weiskopf D; Ramirez SI; Mateus J; Dan JM; Moderbacher CR; Rawlings SA; Sutherland A; Premkumar L; Jadi RS; Marrama D; de Silva AM; Frazier A; Carlin AF; Greenbaum JA; Peters B; Krammer F; Smith DM; Crotty S; Sette A
  • Cell 2020[Jun]; 181 (7): 1489-1501.e15 PMID32473127show ga
  • Understanding adaptive immunity to SARS-CoV-2 is important for vaccine development, interpreting coronavirus disease 2019 (COVID-19) pathogenesis, and calibration of pandemic control measures. Using HLA class I and II predicted peptide ?megapools,? circulating SARS-CoV-2-specific CD8+ and CD4+ T cells were identified in ?70% and 100% of COVID-19 convalescent patients, respectively. CD4+ T cell responses to spike, the main target of most vaccine efforts, were robust and correlated with the magnitude of the anti-SARS-CoV-2 IgG and IgA titers. The M, spike, and N proteins each accounted for 11%?27% of the total CD4+ response, with additional responses commonly targeting nsp3, nsp4, ORF3a, and ORF8, among others. For CD8+ T cells, spike and M were recognized, with at least eight SARS-CoV-2 ORFs targeted. Importantly, we detected SARS-CoV-2-reactive CD4+ T cells in ?40%?60% of unexposed individuals, suggesting cross-reactive T cell recognition between circulating ?common cold? coronaviruses and SARS-CoV-2.
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