BioAcyl Corp |
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| Resource type: Journal Article DOI: 10.1016/j.cell.2020.05.015 ID no. (ISBN etc.): 0092-8674 BibTeX citation key: Grifoni2020 View all bibliographic details |
Categories: BioAcyl Corp Subcategories: Cross immunity Creators: Carlin, Crotty, Dan, de Silva, Frazier, Greenbaum, Grifoni, Jadi, Krammer, Marrama, Mateus, Moderbacher, Peters, Premkumar, Ramirez, Rawlings, Sette, Smith, Sutherland, Weiskopf Collection: Cell |
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| Abstract |
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{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. Graphical Abstract Download : Download high-res image (143KB)Download : Download full-size image}
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