Analysis of the Effectiveness of the Ad26.COV2.S Adenoviral Vector Vaccine for Preventing COVID-19.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 11 2021
Historique:
entrez: 2 11 2021
pubmed: 3 11 2021
medline: 16 11 2021
Statut: epublish

Résumé

Continuous assessment of the effectiveness and safety of the US Food and Drug Administration-authorized SARS-CoV-2 vaccines is critical to amplify transparency, build public trust, and ultimately improve overall health outcomes. To evaluate the effectiveness of the Johnson & Johnson Ad26.COV2.S vaccine for preventing SARS-CoV-2 infection. This comparative effectiveness research study used large-scale longitudinal curation of electronic health records from the multistate Mayo Clinic Health System (Minnesota, Arizona, Florida, Wisconsin, and Iowa) to identify vaccinated and unvaccinated adults between February 27 and July 22, 2021. The unvaccinated cohort was matched on a propensity score derived from age, sex, zip code, race, ethnicity, and previous number of SARS-CoV-2 polymerase chain reaction tests. The final study cohort consisted of 8889 patients in the vaccinated group and 88 898 unvaccinated matched patients. Single dose of the Ad26.COV2.S vaccine. The incidence rate ratio of SARS-CoV-2 infection in the vaccinated vs unvaccinated control cohorts, measured by SARS-CoV-2 polymerase chain reaction testing. The study was composed of 8889 vaccinated patients (4491 men [50.5%]; mean [SD] age, 52.4 [16.9] years) and 88 898 unvaccinated patients (44 748 men [50.3%]; mean [SD] age, 51.7 [16.7] years). The incidence rate ratio of SARS-CoV-2 infection in the vaccinated vs unvaccinated control cohorts was 0.26 (95% CI, 0.20-0.34) (60 of 8889 vaccinated patients vs 2236 of 88 898 unvaccinated individuals), which corresponds to an effectiveness of 73.6% (95% CI, 65.9%-79.9%) and a 3.73-fold reduction in SARS-CoV-2 infections. This study's findings are consistent with the clinical trial-reported efficacy of Ad26.COV2.S and the first retrospective analysis, suggesting that the vaccine is effective at reducing SARS-CoV-2 infection, even with the spread of variants such as Alpha or Delta that were not present in the original studies, and reaffirm the urgent need to continue mass vaccination efforts globally.

Identifiants

pubmed: 34726743
pii: 2785664
doi: 10.1001/jamanetworkopen.2021.32540
pmc: PMC8564583
doi:

Substances chimiques

Ad26COVS1 JT2NS6183B
COVID-19 Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2132540

Commentaires et corrections

Type : CommentIn

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Auteurs

Juan Corchado-Garcia (J)

nference, Cambridge, Massachusetts.

David Zemmour (D)

nference, Cambridge, Massachusetts.

Travis Hughes (T)

nference, Cambridge, Massachusetts.

Hari Bandi (H)

nference, Cambridge, Massachusetts.

Tudor Cristea-Platon (T)

nference, Cambridge, Massachusetts.

Patrick Lenehan (P)

nference, Cambridge, Massachusetts.

Colin Pawlowski (C)

nference, Cambridge, Massachusetts.

Sairam Bade (S)

nference Labs, Murgesh Pallya, Bengaluru, Karnataka, India.

John C O'Horo (JC)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Gregory J Gores (GJ)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Amy W Williams (AW)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Andrew D Badley (AD)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

John Halamka (J)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Abinash Virk (A)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Melanie D Swift (MD)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Tyler Wagner (T)

nference, Cambridge, Massachusetts.

Venky Soundararajan (V)

nference, Cambridge, Massachusetts.
nference Labs, Murgesh Pallya, Bengaluru, Karnataka, India.

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Classifications MeSH