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Ciabattini, Annalisa; Pastore, Gabiria; Lucchesi, Simone; Montesi, Giorgio; Costagli, Simone; Polvere, Jacopo; Fiorino, Fabio; Pettini, Elena; Lippi, Arianna; Ancillotti, Leonardo; Tumbarello, Mario; Fabbiani, Massimiliano; Montagnani, Francesca; Medaglini, Donata
Cells, 06/2023, Letnik: 12, Številka: 13Journal Article
The mRNA vaccines for SARS-CoV-2 have demonstrated efficacy and immunogenicity in the real-world setting. However, most of the research on vaccine immunogenicity has been centered on characterizing the antibody response, with limited exploration into the persistence of spike-specific memory B cells. Here we monitored the durability of the memory B cell response up to 9 months post-vaccination, and characterized the trajectory of spike-specific B cell phenotypes in healthy individuals who received two doses of the BNT162b2 vaccine. To profile the spike-specific B cell response, we applied the tSNE and Cytotree automated approaches. Spike-specific IgA and IgG plasmablasts and IgA activated cells were observed 7 days after the second dose and disappeared 3 months later, while subsets of spike-specific IgG resting memory B cells became predominant 9 months after vaccination, and they were capable of differentiating into spike-specific IgG secreting cells when restimulated in vitro. Other subsets of spike-specific B cells, such as IgM or unswitched IgM IgD or IgG double negative/atypical cells, were also elicited by the BNT162b2 vaccine and persisted up to month 9. The analysis of circulating spike-specific IgG, IgA, and IgM was in line with the plasmablasts observed. The longitudinal analysis of the antigen-specific B cell response elicited by mRNA-based vaccines provides valuable insights into our understanding of the immunogenicity of this novel vaccine platform destined for future widespread use, and it can help in guiding future decisions and vaccination schedules.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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in: SICRIS
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