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TNF-α+ CD4+ T cells dominate the SARS-CoV-2 specific T cell response in COVID-19 outpatients and are associated with durable antibodies

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific CD4+ T cells are likely important in immunity against coronavirus 2019 (COVID-19), but our understanding of CD4+ longitudinal dynamics following infection and of specific features that correlate with the maintenance of neutralizin...

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Published in:Cell Reports Medicine 2022-06, Vol.3 (6), p.100640-100640, Article 100640
Main Authors: van der Ploeg, Kattria, Kirosingh, Adam S., Mori, Diego A.M., Chakraborty, Saborni, Hu, Zicheng, Sievers, Benjamin L., Jacobson, Karen B., Bonilla, Hector, Parsonnet, Julie, Andrews, Jason R., Press, Kathleen D., Ty, Maureen C., Ruiz-Betancourt, Daniel R., de la Parte, Lauren, Tan, Gene S., Blish, Catherine A., Takahashi, Saki, Rodriguez-Barraquer, Isabel, Greenhouse, Bryan, Singh, Upinder, Wang, Taia T., Jagannathan, Prasanna
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Language:English
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Summary:Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-specific CD4+ T cells are likely important in immunity against coronavirus 2019 (COVID-19), but our understanding of CD4+ longitudinal dynamics following infection and of specific features that correlate with the maintenance of neutralizing antibodies remains limited. Here, we characterize SARS-CoV-2-specific CD4+ T cells in a longitudinal cohort of 109 COVID-19 outpatients enrolled during acute infection. The quality of the SARS-CoV-2-specific CD4+ response shifts from cells producing interferon gamma (IFNγ) to tumor necrosis factor alpha (TNF-α) from 5 days to 4 months post-enrollment, with IFNγ-IL-21-TNF-α+ CD4+ T cells the predominant population detected at later time points. Greater percentages of IFNγ-IL-21-TNF-α+ CD4+ T cells on day 28 correlate with SARS-CoV-2-neutralizing antibodies measured 7 months post-infection (⍴ = 0.4, p = 0.01). mRNA vaccination following SARS-CoV-2 infection boosts both IFNγ- and TNF-α-producing, spike-protein-specific CD4+ T cells. These data suggest that SARS-CoV-2-specific, TNF-α-producing CD4+ T cells may play an important role in antibody maintenance following COVID-19. [Display omitted] •SARS-CoV-2-specific CD4+ response shifts from cells producing IFNγ to TNF-α•SARS-CoV-2-specific IFNγ−TNF-α+ CD4+ T cells predominate at later timepoints•IFNγ-TNF-α+ CD4+ T cells correlate with durable SARS-CoV-2-neutralizing antibodies•Post-infection mRNA vaccination boosts both IFNγ+ and TNF-α+ S-specific CD4+ T cells Van der Ploeg et al. provide a better understanding of CD4+ T cell longitudinal dynamics following SARS-CoV-2 infection and specific features that correlate with the maintenance of neutralizing antibodies. Their data suggest that SARS-CoV-2-specific, TNF-α-producing CD4+ T cells may play an important role in antibody maintenance following COVID-19.
ISSN:2666-3791
2666-3791
DOI:10.1016/j.xcrm.2022.100640