AI Article Synopsis

  • The study examines the immunity of individuals who received two doses of an mRNA vaccine alongside different experiences with breakthrough infections and booster doses.
  • It finds that either recovering from a delta variant infection or receiving a booster improves B cell immunity significantly more than just two vaccine doses, especially in the case of breakthrough infections with the omicron variant.
  • Additionally, hybrid immunity from a combination of vaccination and infection leads to better overall immune response than vaccination alone, while T cell responses remain largely unaffected by further exposures.

Article Abstract

The elicited anti-SARS-CoV-2 immunity is becoming increasingly complex with individuals receiving a different number of vaccine doses paired with or without recovery from breakthrough infections with different variants. Here we analyze the immunity of individuals that initially received two doses of mRNA vaccine and either received a booster vaccination, recovered from a breakthrough infection, or both. Our data suggest that two vaccine doses and delta breakthrough infection or three vaccine doses and optionally omicron or delta infection provide better B cell immunity than the initial two doses of mRNA vaccine with or without alpha breakthrough infection. A particularly potent B cell response against the currently circulating omicron variant (B. 1.1.529) was observed for thrice vaccinated individuals with omicron breakthrough infection; a 46-fold increase in plasma neutralization compared to two vaccine doses (p < 0.0001). The T cell response after two vaccine doses is not significantly influenced by additional antigen exposures. Of note, individuals with hybrid immunity show better correlated adaptive immune responses compared to those only vaccinated. Taken together, our data provide a detailed insight into SARS-CoV-2 immunity following different antigen exposure scenarios.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894521PMC
http://dx.doi.org/10.1038/s41467-023-36250-4DOI Listing

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