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Timeline kinetics of protective immunity to SARS-CoV-2 upon primary vaccination and humoral response to variants after booster dose.

Authors :
da Penha Gomes Gouvea M
Lira Machado KLL
de Oliveira YGP
Moulaz IR
Henriques AG
Gouveia TM
Thompson BP
Lança KEM
de Souza Ramos S
Lacerda GCC
Lenzi JPG
de Castro Pimentel F
Miossi JPM
Rassele ML
Camacho LAB
Villela DAM
de Lima SMB
de Souza Azevedo A
Horbach IS
de Araújo MF
Tort LFL
de Oliveira ACA
Siqueira MM
Garcia CC
da Costa-Rocha IA
Campi-Azevedo AC
Peruhype-Magalhães V
da Silva VG
Miyamoto ST
Dos Santos Fantoni RN
Pinto-Neto LF
Magda Domingues C
de Medeiros Junior NF
Burian AP
Teixeira-Carvalho A
Mota LMH
Mill JG
Martins-Filho OA
Valim V
Source :
Vaccine [Vaccine] 2023 Oct 20; Vol. 41 (44), pp. 6514-6528. Date of Electronic Publication: 2023 Sep 01.
Publication Year :
2023

Abstract

New variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have emerged, imposing the need for periodic booster doses. However, whether booster doses should be applied to the entire population or groups, and the booster doses interval, remains unclear. In this study, we evaluated humoral reactivity kinetics from before the first dose to 180 days after the third booster dose in different schedules in a well-controlled health worker cohort. Among the 2,506 employees, the first 500 vaccinated health workers were invited to participate. The third booster dose was administered 8 months after the first dose. Among the invited participants, 470 were included in the study; 258 received inactivated vaccine CoronaVac (VAC group) and 212 received viral vector vaccine ChAdOx1 (AZV group). The groups were homogeneous in terms of age and sex. 347 participants were followed up after the booster dose with AZV or BNT162b2 (Pfizer, BNT group): 63 with VAC/AZV, 117 with VAC/BNT, 72 with the AZV/AZV and 95 with AZV/BNT schedules. Blood samples were collected immediately before, 28 days after each dose and 180 days after the primary vaccination and booster dose. Anti-SARS-CoV-2 antibodies were measured by chemiluminescence and plaque reduction neutralization test (PRNT). Plasma immune mediators were quantified using a multiplex immunoassay. Geometric mean of antibodies increased 28 days after the second dose with 100 % seroconversion rate in both groups and decreased 180 days after the first dose. In the baseline-seropositive VAC group, the levels of plasma immune mediators increased after the second dose. Booster dose was applied at 4-6 months after the primary vaccination. Heterologous booster in VAC or AZV primary vaccinees were effective maintaining the titers of anti-SARS-CoV-2 antibodies even after 6 months of follow-up. The heterologous schedule induced higher and stable antibody reactivity, even after 180 days, protecting to ancestral (Wuhan), Delta, and Omicron variants.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023. Published by Elsevier Ltd.)

Details

Language :
English
ISSN :
1873-2518
Volume :
41
Issue :
44
Database :
MEDLINE
Journal :
Vaccine
Publication Type :
Academic Journal
Accession number :
37661534
Full Text :
https://doi.org/10.1016/j.vaccine.2023.08.022