Incidence and Risk Factors of COVID-19 Vaccine Breakthrough Infections: A Prospective Cohort Study in Belgium.

COVID-19 SARS-CoV-2 breakthrough infection hybrid immunity mRNA booster vaccine mRNA vaccines symptoms vaccination viral vector vaccines

Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
13 04 2022
Historique:
received: 10 03 2022
revised: 07 04 2022
accepted: 08 04 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 27 4 2022
Statut: epublish

Résumé

The objective of this study was to investigate the incidence and risk factors associated with COVID-19 vaccine breakthrough infections. We included all persons ≥18 years that had been fully vaccinated against COVID-19 for ≥14 days, between 1 February 2021 and 5 December 2021, in Belgium. The incidence of breakthrough infections (laboratory confirmed SARS-CoV-2-infections) was determined. Factors associated with breakthrough infections were analyzed using COX proportional hazard models. Among 8,062,600 fully vaccinated adults, we identified 373,070 breakthrough infections with an incidence of 11.2 (95%CI 11.2-11.3)/100 person years. Vaccination with Ad26.COV2.S (HR1.54, 95%CI 1.52-1.56) or ChAdOx1 (HR1.68, 95%CI 1.66-1.69) was associated with a higher risk of a breakthrough infection compared to BNT162b2, while mRNA-1273 was associated with a lower risk (HR0.68, 95%CI 0.67-0.69). A prior COVID-19-infection was protective against a breakthrough infection (HR0.23, 95%CI 0.23-0.24), as was an mRNA booster (HR0.44, 95%CI 0.43-0.45). During a breakthrough infection, those who had a prior COVID-19 infection were less likely to have COVID-19 symptoms of almost all types than naïve persons. We identified risk factors associated with breakthrough infections, such as vaccination with adenoviral-vector vaccines, which could help inform future decisions on booster vaccination strategies. A prior COVID-19 infection lowered the risk of breakthrough infections and of having symptoms, highlighting the protective effect of hybrid immunity.

Identifiants

pubmed: 35458532
pii: v14040802
doi: 10.3390/v14040802
pmc: PMC9029338
pii:
doi:

Substances chimiques

Ad26COVS1 JT2NS6183B
COVID-19 Vaccines 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Veerle Stouten (V)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Pierre Hubin (P)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Freek Haarhuis (F)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Joris A F van Loenhout (JAF)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Matthieu Billuart (M)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Ruben Brondeel (R)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Toon Braeye (T)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Herman Van Oyen (H)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.
Department of Public Health and Primary Care, Ugent, 9000 Gent, Belgium.

Chloé Wyndham-Thomas (C)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

Lucy Catteau (L)

Department of Epidemiology and Public Health, Sciensano, 1050 Brussels, Belgium.

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