Immune recall improves antibody durability and breadth to SARS-CoV-2 variants
Antibody Repertoire
Original antigenic sin
Memory B cell
DOI:
10.1126/sciimmunol.abp8328
Publication Date:
2022-05-12T18:00:50Z
AUTHORS (15)
ABSTRACT
Key features of immune memory are greater and faster antigen-specific antibody responses to repeat infection. In the setting immune-evading viral evolution, it is important understand how far recognition stretches across variants when cells recalled action by invasions. It also recall influences longevity secreted responses. We analyzed SARS-CoV-2 variant recognition; dynamics B cells; over time after infection, vaccination, boosting. find that a two-dose vaccination regimen given natural infection generated longitudinal stability induced maximal magnitudes with enhanced breadth Beta, Gamma, Delta Omicron variants. A homologous third messenger RNA vaccine dose in COVID-naïve individuals conferred cross-variant evenness neutralization potency was equal hybrid immunity plus vaccination. Within unvaccinated who recovered from COVID, observed within subgroup more quickly COVID harbored significantly cross-reactive endemic coronaviruses early These clones map conserved S2 region spike higher somatic hypermutation levels target affinity. conclude antigen challenge histories humans influence not only speed magnitude but functional repertoire composition longevity.
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