Early antibody response in health-care professionals after two doses of SARS-CoV-2 mRNA vaccine (BNT162b2).


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 22 03 2021
revised: 19 04 2021
accepted: 01 05 2021
pubmed: 12 5 2021
medline: 14 9 2021
entrez: 11 5 2021
Statut: ppublish

Résumé

Data on the immune response after two doses of BNT162b2 are so far limited. Previously infected individuals were excluded from pivotal clinical trials and the optimum dose regimen in this population has not been clearly studied. The CRO-VAX HCP study aims to investigate the early antibody response in a population of health-care professionals having received two doses of the BNT162b2 mRNA coronavirus disease 2019 (COVID-19) vaccine. The CRO-VAX HCP study is a multicentre, prospective, interventional study conducted in several sites in Belgium. The study included 231 health-care professional volunteers who received the two-dose regimen of the BNT162b2 mRNA COVID-19 vaccine. Of these, 73 were previously infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and 158 were uninfected and seronegative. In the first group, blood samples were collected at baseline and after 2, 4, 7, 10, 14, 21 and 28 days. In the second group, samples were obtained at baseline and after 14 and 28 days. Antibodies against the SARS-CoV-2 nucleocapsid and the receptor binding domain of the S1 subunit of the spike protein were measured in all individuals at different time-points. In uninfected individuals, 95.5% (95% CI 91.0%-98.2%) developed anti-spike antibodies after 14 days and a 24.9-fold rise (95% CI 21.4%-28.9%) in antibody titre was observed after the second dose. In previously infected individuals, peak antibody response was reached after 7 days (i.e. 6347 U/mL) and the second dose did not lead to significantly higher antibody titres (i.e. 8856-11 911 U/mL). Antibody titres were higher in previously infected individuals. This study supports the concept that a single dose of BNT162b2 would be sufficient in previously infected individuals.

Identifiants

pubmed: 33975007
pii: S1198-743X(21)00224-X
doi: 10.1016/j.cmi.2021.05.004
pmc: PMC8106520
pii:
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0
BNT162 Vaccine N38TVC63NU

Types de publication

Clinical Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1351.e5-1351.e7

Informations de copyright

Copyright © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

Julien Favresse (J)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium; Department of Pharmacy, Namur Research Institute for LIfe Sciences, University of Namur, Belgium. Electronic address: j.favresse@labstluc.be.

Jean-Louis Bayart (JL)

Department of Laboratory Medicine, Clinique St-Pierre, Ottignies, Belgium.

François Mullier (F)

Department of Laboratory Medicine, Université Catholique de Louvain, CHU UCL Namur, Yvoir, Namur, Belgium.

Jean-Michel Dogné (JM)

Department of Pharmacy, Namur Research Institute for LIfe Sciences, University of Namur, Belgium.

Mélanie Closset (M)

Department of Laboratory Medicine, Université Catholique de Louvain, CHU UCL Namur, Yvoir, Namur, Belgium.

Jonathan Douxfils (J)

Department of Pharmacy, Namur Research Institute for LIfe Sciences, University of Namur, Belgium; Qualiblood sa, Namur, Belgium.

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Classifications MeSH