Antibody titres decline 3-month post-vaccination with BNT162b2.


Journal

Emerging microbes & infections
ISSN: 2222-1751
Titre abrégé: Emerg Microbes Infect
Pays: United States
ID NLM: 101594885

Informations de publication

Date de publication:
Dec 2021
Historique:
pubmed: 8 7 2021
medline: 4 8 2021
entrez: 7 7 2021
Statut: ppublish

Résumé

Several studies reported on the humoral response in subjects having received the BNT162b2 mRNA COVID-19 vaccine. However, data on the kinetics of antibodies 3 months post-vaccination are currently lacking and are important to drive the future vaccination strategy. The CRO-VAX HCP study is an ongoing multicentre, prospective and interventional study designed to assess the antibody response in a population of healthcare professionals who had received two doses of the BNT162b2 mRNA COVID-19 vaccine. Two hundred individuals underwent a blood drawn within 2 days before the first vaccine dose. One-hundred and forty-two persons (71%) were categorized as seronegative at baseline while 58 (29%) were seropositive. Samples were then collected after 14, 28, 42, 56, and 90 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. Using a one-compartment kinetics model, the time to maximum concentration was estimated at 36 ± 3 days after the first dose and the estimated half-life of antibodies was 55 days (95% CI: 37-107 days) in seronegative participants. In seropositive participants, the time to maximum concentration was estimated at 24 ± 4 days and the estimated half-life was 80 days (95% CI: 46-303 days). The antibody response was higher in seropositive compared to seronegative participants. In both seropositive and seronegative subjects, a significant antibody decline was observed at 3 months compared to the peak response. Nevertheless, the humoral response remained robust in all participants.

Identifiants

pubmed: 34232116
doi: 10.1080/22221751.2021.1953403
pmc: PMC8300930
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1495-1498

Références

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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, Namur, Belgium.

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, Namur, Belgium.

Marc Elsen (M)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Christine Eucher (C)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Sandrine Van Eeckhoudt (S)

Department of Internal Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Tatiana Roy (T)

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

Gregoire Wieers (G)

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

Christine Laurent (C)

Department of Internal Medicine, Université catholique de Louvain, CHU UCL Namur, Namur, Belgium.

Jean-Michel Dogné (JM)

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

Mélanie Closset (M)

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

Jonathan Douxfils (J)

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

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Classifications MeSH