Article Synopsis

  • The study focuses on how T cells react to SARS-CoV-2 infection by analyzing the immune responses of 99 recovered COVID-19 patients.
  • Researchers use a comprehensive approach, examining 1,925 peptides for class II T cell responses and an additional 5,600 peptides for class I responses across various HLA alleles to ensure broad representation.
  • They identify numerous specific viral epitopes and observe different patterns of immunodominance among CD4 T cells, CD8 T cells, and antibodies, combining findings into epitope megapools for better identification and quantification of T cell responses.

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Article Abstract

T cells are involved in control of SARS-CoV-2 infection. To establish the patterns of immunodominance of different SARS-CoV-2 antigens and precisely measure virus-specific CD4 and CD8 T cells, we study epitope-specific T cell responses of 99 convalescent coronavirus disease 2019 (COVID-19) cases. The SARS-CoV-2 proteome is probed using 1,925 peptides spanning the entire genome, ensuring an unbiased coverage of human leukocyte antigen (HLA) alleles for class II responses. For HLA class I, we study an additional 5,600 predicted binding epitopes for 28 prominent HLA class I alleles, accounting for wide global coverage. We identify several hundred HLA-restricted SARS-CoV-2-derived epitopes. Distinct patterns of immunodominance are observed, which differ for CD4 T cells, CD8 T cells, and antibodies. The class I and class II epitopes are combined into epitope megapools to facilitate identification and quantification of SARS-CoV-2-specific CD4 and CD8 T cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837622PMC
http://dx.doi.org/10.1016/j.xcrm.2021.100204DOI Listing

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