Immunogenicity and safety of COVID-19 booster vaccination: A population-based clinical trial to identify the best vaccination strategy.

COVID-19 Immune response Immunogenicity Neutralizing antibodies Population-based study Vaccination

Journal

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
ISSN: 1873-5967
Titre abrégé: J Clin Virol
Pays: Netherlands
ID NLM: 9815671

Informations de publication

Date de publication:
28 Feb 2024
Historique:
received: 09 03 2023
revised: 21 02 2024
accepted: 25 02 2024
medline: 20 3 2024
pubmed: 20 3 2024
entrez: 19 3 2024
Statut: aheadofprint

Résumé

Various SARS-CoV-2 variants of concerns (VOCs) characterized by higher transmissibility and immune evasion have emerged. Despite reduced vaccine efficacy against VOCs, currently available vaccines provide protection. Population-based evidence on the humoral immune response after booster vaccination is crucial to guide future vaccination strategies and in preparation for imminent COVID-19 waves. This multicenter, population-based cohort study included 4697 individuals ≥18 years of age who received a booster vaccination. Antibody levels against SARS-CoV-2 receptor binding domain (RBD) and neutralizing antibodies against wild-type (WT) virus and Omicron variants were assessed at baseline (day of booster vaccination) and after four weeks. Safety was evaluated daily within the first week using a participant-completed electronic diary. Antibody levels were compared across different vaccination strategies, taking into account individual host factors. Our main model including 3838 participants revealed that individuals who received a booster with mRNA-1273 compared to BNT162b2 vaccine had a significantly higher increase (95 %CI) in anti-RBD-antibody levels (37,707 BAU/mL [34,575-40,839] vs. 27,176 BAU/mL [26,265-28,087]), and of neutralization levels against WT (1,681 [1490-1872] vs. 1141 [1004-1278] and Omicron variant (422 [369-474] vs. 329 [284-374]). Neutralizing antibody titres highly correlated with anti-RBD antibodies, with neutralizing capacity 4.4 fold higher against WT compared to Omicron. No differences in safety were found between the two booster vaccines. Our study underlines the superiority of a booster vaccination with mRNA-1273, independent of the primary vaccination and therefore provides guidance on the vaccination strategy.

Sections du résumé

BACKGROUND BACKGROUND
Various SARS-CoV-2 variants of concerns (VOCs) characterized by higher transmissibility and immune evasion have emerged. Despite reduced vaccine efficacy against VOCs, currently available vaccines provide protection. Population-based evidence on the humoral immune response after booster vaccination is crucial to guide future vaccination strategies and in preparation for imminent COVID-19 waves.
METHODS METHODS
This multicenter, population-based cohort study included 4697 individuals ≥18 years of age who received a booster vaccination. Antibody levels against SARS-CoV-2 receptor binding domain (RBD) and neutralizing antibodies against wild-type (WT) virus and Omicron variants were assessed at baseline (day of booster vaccination) and after four weeks. Safety was evaluated daily within the first week using a participant-completed electronic diary. Antibody levels were compared across different vaccination strategies, taking into account individual host factors.
RESULTS RESULTS
Our main model including 3838 participants revealed that individuals who received a booster with mRNA-1273 compared to BNT162b2 vaccine had a significantly higher increase (95 %CI) in anti-RBD-antibody levels (37,707 BAU/mL [34,575-40,839] vs. 27,176 BAU/mL [26,265-28,087]), and of neutralization levels against WT (1,681 [1490-1872] vs. 1141 [1004-1278] and Omicron variant (422 [369-474] vs. 329 [284-374]). Neutralizing antibody titres highly correlated with anti-RBD antibodies, with neutralizing capacity 4.4 fold higher against WT compared to Omicron. No differences in safety were found between the two booster vaccines.
CONCLUSION CONCLUSIONS
Our study underlines the superiority of a booster vaccination with mRNA-1273, independent of the primary vaccination and therefore provides guidance on the vaccination strategy.

Identifiants

pubmed: 38503118
pii: S1386-6532(24)00023-4
doi: 10.1016/j.jcv.2024.105661
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105661

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

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.

Auteurs

Daniela Sieghart (D)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Claudia A Hana (CA)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Caroline Dürrschmid (C)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Leonhard X Heinz (LX)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Helmuth Haslacher (H)

Department of Laboratory Medicine, Medical University of Vienna, Austria.

Markus Zlesak (M)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Giulia Piccini (G)

Vismederi srl, Siena, Italy.

Alessandro Manenti (A)

Vismederi srl, Siena, Italy.

Emanuele Montomoli (E)

Vismederi srl, Siena, Italy; Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

Anselm Jorda (A)

Department of Clinical Pharmacology, Medical University Vienna, Vienna, Austria.

Clemens Fedrizzi (C)

Department of Clinical Pharmacology, Medical University Vienna, Vienna, Austria.

Timothy Hasenoehrl (T)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Andrej Zdravkovic (A)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Karolina Anderle (K)

Department of Clinical Pharmacology, Medical University Vienna, Vienna, Austria.

Ursula Wiedermann (U)

Center of Pathophysiology, Infectiology & Immunology, Institute of Specific Prophylaxis and Tropical Medicine, Medical University Vienna, Austria.

Susanne Drapalik (S)

Arbeiter-Samariter-Bund Wien, Austria.

Helmut Steinbrecher (H)

Arbeiter-Samariter-Bund Wien, Austria.

Felix Bergmann (F)

Department of Clinical Pharmacology, Medical University Vienna, Vienna, Austria.

Christa Firbas (C)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Galateja Jordakieva (G)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Barbara Wagner (B)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Margherita Leonardi (M)

Vismederi srl, Siena, Italy.

Giulio Pierleoni (G)

Vismederi srl, Siena, Italy.

Matilde Ballini (M)

Vismederi srl, Siena, Italy.

Linda Benincasa (L)

Vismederi srl, Siena, Italy.

Serena Marchi (S)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

Claudia Trombetta (C)

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

Thomas Perkmann (T)

Department of Laboratory Medicine, Medical University of Vienna, Austria.

Richard Crevenna (R)

Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University Vienna, Vienna, Austria.

Markus Zeitlinger (M)

Department of Clinical Pharmacology, Medical University Vienna, Vienna, Austria.

Michael Bonelli (M)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Daniel Aletaha (D)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria. Electronic address: daniel.aletaha@meduniwien.ac.at.

Helga Radner (H)

Department of Internal Medicine III, Division of Rheumatology, Medical University Vienna, Vienna, Austria.

Classifications MeSH