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10.1172/jci.insight.158126

http://scihub22266oqcxt.onion/10.1172/jci.insight.158126
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suck abstract from ncbi


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pmid35133988      JCI+Insight 2022 ; 7 (6): ä
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  • T cell response to intact SARS-CoV-2 includes coronavirus cross-reactive and variant-specific components #MMPMID35133988
  • Jing L; Wu X; Krist MP; Hsiang TY; Campbell VL; McClurkan CL; Favors SM; Hemingway LA; Godornes C; Tong DQ; Selke S; LeClair AC; Pyo CW; Geraghty DE; Laing KJ; Wald A; Gale M Jr; Koelle DM
  • JCI Insight 2022[Mar]; 7 (6): ä PMID35133988show ga
  • SARS-CoV-2 provokes a robust T cell response. Peptide-based studies exclude antigen processing and presentation biology, which may influence T cell detection studies. To focus on responses to whole virus and complex antigens, we used intact SARS-CoV-2 and full-length proteins with DCs to activate CD8 and CD4 T cells from convalescent people. T cell receptor (TCR) sequencing showed partial repertoire preservation after expansion. Resultant CD8 T cells recognize SARS-CoV-2-infected respiratory tract cells, and CD4 T cells detect inactivated whole viral antigen. Specificity scans with proteome-covering protein/peptide arrays show that CD8 T cells are oligospecific per subject and that CD4 T cell breadth is higher. Some CD4 T cell lines enriched using SARS-CoV-2 cross-recognize whole seasonal coronavirus (sCoV) antigens, with protein, peptide, and HLA restriction validation. Conversely, recognition of some epitopes is eliminated for SARS-CoV-2 variants, including spike (S) epitopes in the Alpha, Beta, Gamma, and Delta variant lineages.
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