Early antibody response in health-care professionals after two doses of SARS-CoV-2 mRNA vaccine (BNT162b2).
Adult
Aged
Antibodies, Viral
/ blood
BNT162 Vaccine
Belgium
COVID-19
/ epidemiology
COVID-19 Vaccines
/ administration & dosage
Case-Control Studies
Drug Administration Schedule
Female
Health Personnel
Humans
Immunity, Humoral
Male
Middle Aged
Prospective Studies
SARS-CoV-2
/ immunology
Spike Glycoprotein, Coronavirus
/ immunology
Time Factors
Young Adult
Antibody
BNT162b2
Coronavirus disease 2019
Humoral response
Severe acute respiratory syndrome coronavirus 2
Vaccine
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
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.e7Informations de copyright
Copyright © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.