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10.1101/2022.01.23.22269497

http://scihub22266oqcxt.onion/10.1101/2022.01.23.22269497
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suck abstract from ncbi


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pmid35118477      medRxiv 2022 ; ä (ä): ä
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  • T cell response to intact SARS-CoV-2 includes coronavirus cross-reactive and variant-specific components #MMPMID35118477
  • 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; Koelle DM
  • medRxiv 2022[Jan]; ä (ä): ä PMID35118477show ga
  • SARS-CoV-2 provokes a brisk T cell response. Peptide-based studies exclude antigen processing and presentation biology and 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 DC to activate CD8 and CD4 T cells from convalescent persons. T cell receptor (TCR) sequencing showed partial repertoire preservation after expansion. Resultant CD8 T cells recognize SARS-CoV-2-infected respiratory 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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