Guihai Liu, Elie Antoun, Anastasia Fries, Xuan Yao, Zixi Yin, Danning Dong, Wenbo Wang, Peter A. C. Wing, Wanwisa Dejnirattisa, Piyada Supasa, Chang Liu, Timothy Rostron, Craig Waugh, Kevin Clark, Paul Sopp, Jeremy Fry, Iolanda Vendrell, Jane A. McKeating, Juthathip Mongkolsapaya, Gavin Screaton, Benedikt M. Kessler, Román Fischer, Graham S. Ogg, Alexander J. Mentzer, Julian C. Knight, Yanchun Peng, Tao Dong
Abstract The recent COVID-19 pandemic left behind the lingering question as whether new variants of concern might cause further waves of infection. Thus, it is important to investigate the long-term protection gained via vaccination or exposure to the SARS-CoV-2 virus. Here we compare the evolution of memory T-cell responses following primary infection with subsequent antigen exposures. Single-cell TCR analysis of three dominant SARS-CoV-2 spike-specific CD4 + T-cell responses identifies the dominant public TCRα clonotypes pairing with diverse TCRβ clonotypes that associated with mild disease at primary infection. These clonotypes are found at higher frequencies in pre-pandemic repertoires compared to other epitope-specific clonotypes. Longitudinal transcriptomics and TCR analysis, combined with functional evaluation, reveals that the clonotypes persisting 3–4 years post initial infection exhibit distinct functionality compared to those that were lost. Furthermore, spike-specific CD4 + T cells at this time point show decreased Th1 signatures and enhanced GZMA -driven cytotoxic transcriptomic profiles that were independent of TCR clonotype and associated with viral suppression. In summary, we identify common public TCRs used by immunodominant spike-specific memory CD4 + T-cells, associated with mild disease outcome, which likely play important protective roles to subsequent viral infection events.