Evaluation of Antibody Kinetics Following COVID-19 Vaccination in Greek SARS-CoV-2 Infected and Naïve Healthcare Workers

Author:

Pavlidis George1ORCID,Giannoulis Vasileios2,Pirounaki Maria3,Lampropoulos Ioannis C.4ORCID,Siafi Eirini1,Nitsa Alkippi5,Pavlou Efthymia2,Xanthaki Anna5,Perlepe Garyfallia4ORCID,Fortis Sotirios P.6,Charalambous George1,Kampolis Christos F.1,Pantazopoulos Ioannis47ORCID

Affiliation:

1. Department of Emergency Medicine, Hippokration General Hospital, 11527 Athens, Greece

2. Transfusion and Haemophilia Centre, Hippokration General Hospital, 11527 Athens, Greece

3. Second Department of Internal Medicine, National and Kapodistrian University of Athens, School of Medicine, Hippokration General Hospital, 11527 Athens, Greece

4. Respiratory Medicine Department, Faculty of Medicine, University of Thessaly, 41500 Larissa, Greece

5. Microbiology Department, Hippokration General Hospital, 11527 Athens, Greece

6. Laboratory of Reliability and Quality Control in Laboratory Hematology (HemQcR), Department of Biomedical Sciences, School of Health and Caring Sciences, University of West Attica, 12243 Egaleo, Greece

7. Department of Emergency Medicine, Faculty of Medicine, University of Thessaly, 41500 Larissa, Greece

Abstract

We investigated the antibody kinetics after vaccination against COVID-19 in healthcare workers of a Greek tertiary hospital. Eight hundred and three subjects were included, of whom 758 (94.4%) received the BNT162b2 vaccine (Pfizer-BioNTech), eight (1%) mRNA-1273 (Moderna), 14 (1.7%) ChAdOx1 (Oxford-AstraZeneca) and 23 (2.9%) Ad26.COV2.S (Janssen). Before the second dose, at 2, 6 and 9 months after the second dose and at 2 and 6 months after the third dose, anti-spike IgG were quantified by the chemiluminescence microparticle immunoassay method. One hundred subjects were infected before vaccination (group A), 335 were infected after receiving at least one vaccine dose (group B), while 368 had never been infected (group C). Group A presented a greater number of hospitalizations and reinfections compared to group B (p < 0.05). By multivariate analysis, younger age was associated with an increased risk of reinfection (odds ratio: 0.956, p = 0.004). All subjects showed the highest antibody titers at 2 months after the second and third dose. Group A showed higher antibody titers pre-second dose, which remained elevated 6 months post-second dose compared to groups B and C (p < 0.05). Pre-vaccine infection leads to rapid development of high antibody titer and a slower decline. Vaccination is associated with fewer hospitalizations and fewer reinfections.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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