Authors
Ryan E Wiegand, Sean Chickery, Duck-Hye Yang, Sarah W Ball, Malini B DeSilva, Kristin Dascomb, Stephanie A Irving, Karthik Natarajan, Nicola P Klein, Shaun J Grannis, Toan C Ong, Elizabeth A K Rowley, Adam Yates, Yan Zhuang, Sarah Wilson, Charlene E McEvoy, Inih J Essien, Omobosola O Akinsete, Allison L Naleway, Padma Koppolu, Ousseny Zerbo, John R Hansen, Karen B Jacobson, Lawrence Block, Brian E Dixon, Thomas Duszynski, Colin Rogerson, Michelle A Barron, Catia Chavez, Josephine Mak, Allison Avrich Ciesla, Monica Godfrey, Amber Kautz, Morgan Najdowski, Ruth Link-Gelles, Jennifer DeCuir, Amanda B Payne
Published in
JAMA network open. Volume 9. Issue 6. Pages e2625152. Jun 01, 2026. Epub Jun 01, 2026.
Abstract
The 2025-2026 COVID-19 vaccine, targeting JN.1 and JN.1-derived sublineages, became available in the US in September 2025.
To assess the estimated interim effectiveness of 2025-2026 COVID-19 vaccines against medically attended COVID-19 among immunocompetent adults aged 18 years or older in the US.
This case-control study used a test-negative design to investigate patient encounters captured in the Virtual SARS-CoV-2, Influenza, and Other Respiratory Viruses Network, an electronic medical record-based network of health care systems (253 emergency departments/urgent cares [ED/UCs] and 179 hospitals in 7 states) from September 3, 2025, to December 31, 2025. Patient encounters with COVID-19-like illness and a molecular or antigen SARS-CoV-2 test 10 days before to 3 days after the encounter date were included.
2025-2026 COVID-19 vaccination regardless of prior COVID-19 vaccination.
The main outcomes were COVID-19-associated ED/UC encounters and COVID-19-associated hospitalizations. Cases were defined as encounters with a positive molecular or antigen SARS-CoV-2 test and controls as encounters with a negative molecular SARS-CoV-2 test. The odds of 2025-2026 COVID-19 vaccination among cases and controls, adjusting for confounders, were compared and used to estimate vaccine effectiveness (VE) as (1 - adjusted odds ratio) × 100%.
In 85 725 ED/UC encounters among adults aged 18 years and older (51 841 [60%] aged 18-64 years; 51 775 female [60%]), 206 of 3941 cases (5%) and 9453 of 81 784 controls (12%) received a 2025-2026 COVID-19 vaccination. Estimated VE against COVID-19-associated ED/UC encounters was 50% (95% CI, 42%-57%; median [IQR] time since 2025-2026 COVID-19 vaccine dose receipt, 47 [27-69] days). In 26 073 hospitalizations with a COVID-19-like illness (17 530 [67%] aged ≥65 years; 13 985 female [54%]), 60 of 1022 cases (6%) received a 2025-2026 COVID-19 vaccination compared with 3080 of 25 051 controls (12%). Estimated VE against COVID-19-associated hospitalization was 55% (95% CI, 41%-66%; median [IQR] time since 2025-2026 COVID-19 vaccine dose receipt, 46 [26-68] days). Among patients aged 65 years or older, estimated VE against ED/UC encounters was 48% (95% CI, 37%-56%; median [IQR] time since dose receipt, 48 [27-69] days; 33 884 encounters) and against hospitalization was 53% (95% CI, 37%-65%; median [IQR] time since dose receipt, 46 [26-69] days; 17 530 hospitalizations).
In this study, receipt of 2025-2026 COVID-19 vaccination was associated with additional protection beyond existing immunity in adults against medically attended COVID-19, including ED/UC encounters and hospitalizations, compared with no receipt of a 2025-2026 vaccine dose. These findings suggest that adults can reduce their likelihood of severe COVID-19-associated outcomes by obtaining a 2025-2026 COVID-19 vaccination.
PMID:
42334917
Bibliographic data and abstract were imported from PubMed on 24 Jun 2026.
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