AI Article Synopsis

  • The COVID-19 pandemic has severely impacted global health, economy, and society, with vaccinations being key to returning to normal.
  • A study compared the immune responses to the BNT162b2 and AZD1222 vaccines, analyzing antibody levels and T-cell responses in nearly 1,200 individuals over time.
  • Results showed that BNT162b2 produced higher antibody levels than AZD1222, but both vaccines effectively generated T-cells and provided sufficient immunity after the first dose, supporting their use for sero-surveillance efforts.

Article Abstract

COVID-19 pandemic has hit people's health, economy, and society worldwide. Great confidence in returning to normality has been placed in the vaccination campaign. The knowledge of individual immune profiles and the time required to achieve immunological protection is crucial to choose the best vaccination strategy. We compared anti-S1 antibody levels produced over time by BNT162b2 and AZD1222 vaccines and evaluated the induction of antigen-specific T-cells. A total of 2569 anti-SARS-CoV-2 IgG determination on dried blood spot samples were carried out, firstly in a cohort of 1181 individuals at random time-points, and subsequently, in an independent cohort of 88 vaccinated subjects, up to the seventeenth week from the first dose administration. Spike-specific T-cells were analysed in seronegative subjects between the two doses. AZD1222 induced lower anti-S1 IgG levels as compared to BNT162b2. Moreover, 40% of AZD1222 vaccinated subjects and 3% of BNT162b2 individuals resulted in seronegative during all the time-points, between the two doses. All these subjects developed antigen-specific T cells, already after the first dose. These results suggest that this test represents an excellent tool for a wide sero-surveillance. Both vaccines induce a favourable immune profile guaranteeing efficacy against severe adverse effects of SARS-CoV-2 infection, already after the first dose administration.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391252PMC
http://dx.doi.org/10.3390/biomedicines9081035DOI Listing

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