Effectiveness over time of a primary series of the original monovalent COVID-19 vaccines in adults in the United States

With data from 2 US claims databases (Optum, CVS Health) supplemented with Immunization Information System COVID-19 vaccine records, we evaluated overall and time-specific vaccine effectiveness (VE) of an initial primary series for 3 monovalent COVID-19 vaccines-BNT162b2, mRNA-1273, and JNJ-7836735-in adults (18-64 years). Vaccinated individuals were matched to unvaccinated comparators, and we estimated VE against any medically diagnosed COVID-19 and hospital/emergency department (ED)-diagnosed COVID-19. Additionally, we estimated VE by era of predominant variants, in subgroups, and compared across vaccine brands. The cohorts consisted of 341,097 (Optum) and 1,151,775 (CVS Health) matched pairs for BNT162b2; 201,604 (Optum) and 651,545 (CVS Health) for mRNA-1273; and 49,285 (Optum) and 149,813 (CVS Health) for JNJ-7836735. The study period began 11 December 2020 (date of first COVID-19 vaccine availability in the US) and ended 15 January 2022 in Optum and 31 March 2022 in CVS Health. Summary VE estimates from meta-analysis against hospital/ED-diagnosed COVID-19 were: BNT162b2, 77% (95% CI, 76%-78%); mRNA-1273, 84% (95% CI, 83%-85%), JNJ-7836735 66% (95% CI, 63%-68%). VE estimates were higher for hospital/ED-diagnosed COVID-19 than for medically diagnosed COVID-19, and VE estimates were highest in adults receiving mRNA-1273 for both outcomes. VE was sustained for approximately 7 months for medically diagnosed and up to 9 months for hospital/ED-diagnosed COVID-19. VE differed by brand and variant era. Ongoing real-world surveillance of COVID-19 vaccines using robust data sources and methodology is needed as new variants and recommendations for updated vaccines have evolved.

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Journal
PLoS ONE
Published
2025-05-06
DOI
https://doi.org/10.1371/journal.pone.0320434
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Effectiveness over time of a primary series of the original monovalent COVID-19 vaccines in adults in the United States

Ron Parambi, John D. Seeger, Steven A. Anderson, Tainya C. Clarke et al.
PLoS ONE
SARS-CoV-2 and COVID-19 Research
article

Effectiveness over time of a primary series of the original monovalent COVID-19 vaccines in adults in the United States

Ron Parambi, John D. Seeger, Steven A. Anderson, Tainya C. Clarke, Michael Miller, Jie Deng, Lisa B. Weatherby, Sylvia Cho, Rachel P. Ogilvie, Mary S. Anthony, Michael Wernecke, J. Bradley Layton, Yixin Jiao, Jennifer Song, Lauren Peetluk, Cheryl N. McMahill‐Walraven, Christine Bui, Jessica Rose Hervol, Hui‐Lee Wong, Joann F. Gruber, An‐Chi Lo, Morgan M. Richey, Yoganand Chillarige, Elizabeth Bell, Patricia C. Lloyd, Kandace L. Amend, Richard A. Forshee, Djeneba Audrey Djibo, Dóra Illei, Grace Wenya Yang, Azadeh Shoaibi
article en

Abstract

With data from 2 US claims databases (Optum, CVS Health) supplemented with Immunization Information System COVID-19 vaccine records, we evaluated overall and time-specific vaccine effectiveness (VE) of an initial primary series for 3 monovalent COVID-19 vaccines-BNT162b2, mRNA-1273, and JNJ-7836735-in adults (18-64 years). Vaccinated individuals were matched to unvaccinated comparators, and we estimated VE against any medically diagnosed COVID-19 and hospital/emergency department (ED)-diagnosed COVID-19. Additionally, we estimated VE by era of predominant variants, in subgroups, and compared across vaccine brands. The cohorts consisted of 341,097 (Optum) and 1,151,775 (CVS Health) matched pairs for BNT162b2; 201,604 (Optum) and 651,545 (CVS Health) for mRNA-1273; and 49,285 (Optum) and 149,813 (CVS Health) for JNJ-7836735. The study period began 11 December 2020 (date of first COVID-19 vaccine availability in the US) and ended 15 January 2022 in Optum and 31 March 2022 in CVS Health. Summary VE estimates from meta-analysis against hospital/ED-diagnosed COVID-19 were: BNT162b2, 77% (95% CI, 76%-78%); mRNA-1273, 84% (95% CI, 83%-85%), JNJ-7836735 66% (95% CI, 63%-68%). VE estimates were higher for hospital/ED-diagnosed COVID-19 than for medically diagnosed COVID-19, and VE estimates were highest in adults receiving mRNA-1273 for both outcomes. VE was sustained for approximately 7 months for medically diagnosed and up to 9 months for hospital/ED-diagnosed COVID-19. VE differed by brand and variant era. Ongoing real-world surveillance of COVID-19 vaccines using robust data sources and methodology is needed as new variants and recommendations for updated vaccines have evolved.

PLoS ONEVol. 20(5)
NatureServe (US), Center for Biologics Evaluation and Research (US), RTI International (US), New England College of Optometry (US), Acumen (United States) (US), RTI Health Solutions (US), Campbell Collaboration (NO)
U.S. Food and Drug Administration
Good health and well-being
Openalex Percentile: Top 87%
SARS-CoV-2 and COVID-19 Research
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