PT - JOURNAL ARTICLE AU - Alison Tarke AU - John Sidney AU - Conner K Kidd AU - Jennifer M. Dan AU - Sydney I. Ramirez AU - Esther Dawen Yu AU - Jose Mateus AU - Ricardo da Silva Antunes AU - Erin Moore AU - Paul Rubiro AU - Nils Methot AU - Elizabeth Phillips AU - Simon Mallal AU - April Frazier AU - Stephen A. Rawlings AU - Jason A. Greenbaum AU - Bjoern Peters AU - Davey M. Smith AU - Shane Crotty AU - Daniela Weiskopf AU - Alba Grifoni AU - Alessandro Sette TI - Comprehensive analysis of T cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases AID - 10.1101/2020.12.08.416750 DP - 2020 Jan 01 TA - bioRxiv PG - 2020.12.08.416750 4099 - http://biorxiv.org/content/early/2020/12/09/2020.12.08.416750.short 4100 - http://biorxiv.org/content/early/2020/12/09/2020.12.08.416750.full AB - 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 studied epitope-specific T cell responses of approximately 100 convalescent COVID-19 cases. The SARS-CoV-2 proteome was probed using 1,925 peptides spanning the entire genome, ensuring an unbiased coverage of HLA alleles for class II responses. For HLA class I, we studied an additional 5,600 predicted binding epitopes for 28 prominent HLA class I alleles, accounting for wide global coverage. We identified several hundred HLA-restricted SARS-CoV-2-derived epitopes. Distinct patterns of immunodominance were observed, which differed for CD4+ T cells, CD8+ T cells, and antibodies. The class I and class II epitopes were combined into new epitope megapools to facilitate identification and quantification of SARS-CoV-2-specific CD4+ and CD8+ T cells.Competing Interest StatementA.S. is a consultant for Gritstone, Flow Pharma, Merck, Epitogenesis, Gilead and Avalia. S.C. is a consultant for Avalia. All other authors declare no conflict of interest. LJI has filed for patent protection for various aspects of vaccine design and identification of specific epitopes.