Comparative effectiveness and duration of protection of ChAdOx1, CoronaVac, BNT162b2, mRNA-1273, and Ad26.COV2.S COVID-19 vaccines for symptomatic and hospitalized Mu, Delta, and Omicron: A test-negative case-control study.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
06 10 2023
Historique:
received: 02 04 2023
revised: 23 08 2023
accepted: 25 08 2023
medline: 3 10 2023
pubmed: 8 9 2023
entrez: 7 9 2023
Statut: ppublish

Résumé

We carried out a study to estimate the vaccine effectiveness (VE) of homologous vaccination schedules against COVID-19, using data from mandatory information systems from Bogota, Colombia. A test-negative case-control study in adults from Bogota (Colombia), between March 1st of 2021 and February 25th of 2022. We assess VE among symptomatic COVID-19 cases during the Mul, Delta, and Omicron predominance periods in Bogota, with controls matched by sex, age (±5 years), and date of testing (±7 days), using a case:control ratio of 1:1. We selected homologous vaccination schedules with ChAdOx1, CoronaVac, BNT162b2, mRNA-1273, and Ad26.COV2.S. VE was reported as one minus the odds ratio in adjusted conditional logistic regressions, with their 95% confidence intervals (CI). A p-value < 0.05 was considered statistically significant. 52,913 cases were matched to controls, 16,722 for Mu, 14,094 for Delta, and 22,097 for Omicron. VE was high against COVID-19 during Mu weeks with full vaccination using the monovalent BNT162b2 (VE: 69; 95% CI, 65 to 72) vaccine and ChAdOx1 (VE: 64; 95% CI, 31 to 81) and significantly lower with CoronaVac (P < 0.001) and Ad26.COV2.S (P = 0.005). During Delta, VE against COVID-19 was higher with BNT162b2 (VE: 55; 95% CI, 51 to 58). The VE for COVID-19 cases during Omicron was higher with a booster dose of monovalent BNT162b2 (VE: 45; 95% CI, 34 to 54). The VE of primary series and booster for ChAdOx1, Ad26.COV2.S, and CoronaVac did not show protection for Omicron. Our study provides further evidence on the protective effect of mRNA vaccines for Omicron, and warrant that the duration of protection against symptomatic infection may last for only a few months.

Identifiants

pubmed: 37679278
pii: S0264-410X(23)01028-9
doi: 10.1016/j.vaccine.2023.08.072
pii:
doi:

Substances chimiques

sinovac COVID-19 vaccine 0
COVID-19 Vaccines 0
2019-nCoV Vaccine mRNA-1273 EPK39PL4R4
BNT162 Vaccine 0
Ad26COVS1 JT2NS6183B

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

6291-6299

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Nelson Alvis-Zakzuk reports a relationship with Pfizer that includes: consulting or advisory and funding grants. Lina Moyano reports a relationship with Pfizer that includes: consulting or advisory.

Auteurs

Angel Paternina-Caicedo (A)

ALZAK Foundation, Cartagena, Colombia; Universidad del Sinú, Cartagena, Colombia. Electronic address: apaterninacaicedo@tulane.edu.

David Santiago Quevedo (DS)

Secretary of Health, Bogota, Colombia.

Diana Sofía Ríos (DS)

Secretary of Health, Bogota, Colombia.

Diane Moyano (D)

Secretary of Health, Bogota, Colombia.

Nelson Alvis-Guzmán (N)

ALZAK Foundation, Cartagena, Colombia; Universidad de Cartagena, Cartagena, Colombia.

Nelson Rafael Alviz-Zakzuk (NR)

ALZAK Foundation, Cartagena, Colombia.

Fernando Salcedo (F)

ALZAK Foundation, Cartagena, Colombia.

Lina Moyano (L)

ALZAK Foundation, Cartagena, Colombia.

Javier Ramírez-Suarez (J)

Universidad Nacional de Colombia, Bogotá, Colombia.

Adrian D Smith (AD)

University of Oxford, Oxford, UK.

Fernando De la Hoz-Restrepo (F)

Universidad Nacional de Colombia, Bogotá, Colombia.

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Classifications MeSH