Abstract The current COVID-19 pandemic represents a global challenge. A better understanding of the immune response against SARS-CoV-2 is key to unveil the differences in disease severity and to develop future vaccines targeting novel SARS-CoV-2 variants. Feature barcode technology combined with CITE-seq antibodies and DNA-barcoded peptide-MHC I Dextramer reagents enabled us to identify relevant SARS-CoV-2-derived epitopes and compare epitope-specific CD8 + T cell populations between mild and severe COVID-19. We identified a strong CD8 + T cell response against an S protein-derived epitope. CD8 + effector cells in severe COVID-19 displayed hyperactivation, T cell exhaustion and were missing characteristics of long-lived memory T cells. We identify A*0101 WTAGAAAYY as an immunogenic CD8 + T cell epitope with the ability to drive clonal expansion. We provide an in-depth characterization of the CD8 + T cell-mediated response to SARS-CoV-2 infection which will be relevant for the development of molecular and targeted therapies and potential adjustments of vaccination strategies.

Dissecting CD8+ T cell pathology of severe SARS-CoV-2 infection by single-cell epitope mapping