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B cell analyses after SARS-CoV-2 mRNA third vaccination reveals a hybrid immunity like antibody response.

Emanuele AndreanoIda PacielloGiulio PierleoniGiulia PicciniValentina AbbientoGiada AntonelliPiero PileriNoemi ManganaroElisa PantanoGiuseppe MaccariSilvia MarcheseLorena DonniciLinda BenincasaGinevra GiglioliMargherita LeonardiConcetta De SantiMassimiliano FabbianiIlaria RancanMario TumbarelloFrancesca MontagnaniClaudia SalaDuccio MediniRaffaele de FrancescoEmanuele MontomoliRino Rappuoli
Published in: Nature communications (2023)
The continuous evolution of SARS-CoV-2 generated highly mutated variants able to escape natural and vaccine-induced primary immunity. The administration of a third mRNA vaccine dose induces a secondary response with increased protection. Here we investigate the longitudinal evolution of the neutralizing antibody response in four donors after three mRNA doses at single-cell level. We sorted 4100 spike protein specific memory B cells identifying 350 neutralizing antibodies. The third dose increases the antibody neutralization potency and breadth against all SARS-CoV-2 variants as observed with hybrid immunity. However, the B cell repertoire generating this response is different. The increases of neutralizing antibody responses is largely due to the expansion of B cell germlines poorly represented after two doses, and the reduction of germlines predominant after primary immunization. Our data show that different immunization regimens induce specific molecular signatures which should be considered while designing new vaccines and immunization strategies.
Keyphrases
  • sars cov
  • single cell
  • respiratory syndrome coronavirus
  • binding protein
  • electronic health record
  • gene expression
  • oxidative stress
  • genome wide
  • big data
  • coronavirus disease
  • single molecule
  • amino acid