AI Article Synopsis

  • SARS-CoV-2 infection results in varying immune responses, with neutralizing antibodies generally protecting against reinfection.
  • The study investigated mild cases linked to a single event, revealing sex-specific differences in T cell responses and their correlation with antibody levels, particularly in males.
  • Additionally, single-cell immunoprofiling indicated variations in type I IFN signaling that may influence antibody production, emphasizing the importance of sex-based factors in immune responses to SARS-CoV-2.

Article Abstract

SARS-CoV-2 infection leads to a broad range of outcomes and immune responses, with the development of neutralizing antibodies generally correlated with protection against reinfection. Here, we have characterized both neutralizing activity and T cell responses in a cluster of subjects with mild disease linked to a single spreading event. Surprisingly, we observed sex-specific associations between spike- and particularly nucleoprotein-specific T cell responses and neutralization, with pro-inflammatory cytokines being linked to higher titers only in males. Using single cell immunoprofiling, which provided matched transcriptome and T-cell receptor (TCR) profiles in restimulated CD4 + and CD8 + cells from these subjects, we identified differences in type I IFN signaling that may underlie this difference in antibody generation. Finally, we also identified several TCRs associated with cytokine producing T cells. Altogether, our work maps the breadth of immunological outcomes of SARS-CoV2 infections and highlight the potential role of sex-specific feedback loops during the generation of neutralizing antibodies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8936123PMC
http://dx.doi.org/10.21203/rs.3.rs-1416969/v1DOI Listing

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