4.5 Article

Longitudinal determination of BNT162b2 vaccine induced strongly binding SARS-CoV-2 IgG antibodies in a cohort of Romanian healthcare workers

Journal

VACCINE
Volume 40, Issue 37, Pages 5445-5451

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2022.07.040

Keywords

SARS-CoV-2 immune response; Comirnaty; Antibody waning; Elisa assay; IgG antibodies

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Mass vaccination against COVID-19 is crucial for slowing the spread of the virus. A study on Romanian healthcare workers found that individuals who were previously infected with the virus had a quicker immune response after vaccination compared to those who were not infected. The previously infected group also maintained higher levels of IgG antibodies throughout the six-month observation period. A booster dose increased IgG antibody levels in the infection-naive group.
Mass vaccination against the disease caused by the novel coronavirus (COVID-19) was a crucial step in slowing the spread of SARS-CoV-2 in 2021. Even in the face of new variants, it still remains extremely important for reducing hospitalizations and COVID-19 deaths. In order to better understand the short -and long-term dynamics of humoral immune response, we present a longitudinal analysis of post -vaccination IgG levels in a cohort of 166 Romanian healthcare workers vaccinated with BNT162b2 with weekly follow-up until 35 days past the first dose and monthly follow-up up to 6 months post -vaccination. A subset of the patients continued with follow-up after 6 months and either received a boos-ter dose or got infected during the Delta wave in Romania. Tests were carried out on 1694 samples using a CE-marked IgG ELISA assay developed in-house, containing S1 and N antigens of the wild type virus. Participants infected with SARS-CoV-2 before vaccination mount a quick immune response, reaching peak IgG levels two weeks after the first dose, while IgG levels of previously uninfected participants mount gradually, increasing abruptly after the second dose. Overall higher IgG levels are maintained for the previously infected group throughout the six month primary observation period (e.g. 36-65 days after the first dose, the median value in the previously infected group is 5.29 AU/ml, versus 3.58 AU/ml in the infection naive group, p less than 0.001). The decrease of IgG levels is gradual, with lower median val-ues in the infection naive cohort even 7-8 months after vaccination, compared to the previously infected cohort (0.7 AU/ml versus 1.29 AU/ml, p = 0.006). Administration of a booster dose yielded higher median IgG antibody levels than post second dose in the infection naive group and comparable levels in the pre-viously infected group. (c) 2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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