Persistence of Anti-S1 IgG against SARS-CoV-2 Eight Months after the Booster Dose of Vaccine in Naive and Previously Infected Healthcare Workers.
Sonia AlgarateLaura SerranoJessica BuenoBeatriz Herrero-CortinaElena AlvaradoMaría T González-BarrigaMaría DuconsJesica Montero-MarcoSara ArnalBeatriz AchaMaría RiesgoAna TaboadaPilar Sanz-BurilloCristina YusteRafael Benito-Ruescanull On Behalf Of The Ripovac Study GroupPublished in: International journal of molecular sciences (2023)
Our aim was to evaluate the immune response of healthcare workers included in the RIPOVAC study, after receiving a booster dose (third dose), in terms of intensity and persistence of induced antibodies. In the second phase of the RIPOVAC study, between December 2021 and January 2022, eight months after the second dose, 389 voluntary, immunocompetent, non-pregnant healthcare workers received a booster dose of SARS-CoV-2 vaccine, and a serum sample was obtained. Two groups of patients were established: with and without previous SARS-CoV-2 infection. In order to quantify anti-S1 IgG (AU/mL) we used CMIA (Abbott). All of the health workers were anti-S IgG positive 8 months after receiving the booster dose of the vaccine, with a mean of 17,040 AU/mL. In 53 patients without previous infection, antibody levels increased by a mean of 10,762 AU/mL. This figure is seven times higher than the one produced after the second dose (1506 AU/mL). The booster dose produces a robust elevation of the antibody level, which persists at 8 months, with levels significantly higher than those reached after the second dose, which allow one to predict a persistence of more than one year. The study demonstrates the efficacy of the booster dose of anti-SARS-CoV-2 vaccines.
Keyphrases
- sars cov
- immune response
- end stage renal disease
- ejection fraction
- healthcare
- sensitive detection
- chronic kidney disease
- peritoneal dialysis
- pregnant women
- reduced graphene oxide
- hiv infected
- oxidative stress
- coronavirus disease
- high intensity
- risk assessment
- toll like receptor
- stress induced
- antiretroviral therapy
- human health