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Comparative Analysis of Antibody Titers against the Spike Protein of SARS-CoV-2 Variants in Infected Patient Cohorts and Diverse Vaccination Regimes.

Alexandru OdainicJasper SpitzerJennifer Barbara SzlapaSimon SchadeTim Jonas KrämerJakob NeubergerChristian BodeFolkert SteinhagenRicarda Maria SchmithausenGero WilbringEsther SibNico Tom MuttersFrederik RabenschlagLisa KettelMaike WoznitzaKathrin van BremenTina PeersGez MedingerAnushka KudaliyanageMaike KreutzenbeckUlrike StrubeJoseph M JohnsonDawn MattoonAndrew J BallStefan ScoryRichard McGuireChristian PutensenZeinab AbdullahCatharina LatzSusanne Viktoria Schmidt
Published in: International journal of molecular sciences (2022)
The presence of neutralizing antibodies against SARS-CoV-2 correlates with protection against infection and severe COVID-19 disease courses. Understanding the dynamics of antibody development against the SARS-CoV-2 virus is important for recommendations on vaccination strategies and on control of the COVID-19 pandemic. This study investigates the dynamics and extent of α-Spike-Ab development by different vaccines manufactured by Johnson & Johnson, AstraZeneca, Pfizer-BioNTech and Moderna. On day 1 after vaccination, we observed a temporal low-grade inflammatory response. α-Spike-Ab titers were reduced after six months of vaccination with mRNA vaccines and increased 14 days after booster vaccinations to a maximum that exceeded titers from mild and critical COVID-19 and Long-COVID patients. Within the group of critical COVID-19 patients, we observed a trend for lower α-Spike-Ab titers in the group of patients who survived COVID-19. This trend accompanied higher numbers of pro-B cells, fewer mature B cells and a higher frequency of T follicular helper cells. Finally, we present data demonstrating that past infection with mild COVID-19 does not lead to long-term increased Ab titers and that even the group of previously infected SARS-CoV-2 patients benefit from a vaccination six months after the infection.
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