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Estimated Effectiveness of 2024-2025 COVID-19 Vaccination Against Severe COVID-19
Kevin C Ma1, Alexander Webber1, Adam S Lauring2,3
1Coronavirus and Other Respiratory Viruses Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia.
Insights
The 2024-2025 COVID-19 vaccines demonstrated effectiveness against hospitalization and severe outcomes, including invasive mechanical ventilation or death, amidst evolving SARS-CoV-2 JN.1 descendant lineages. Continued monitoring of vaccine effectiveness is crucial for guiding future vaccination strategies and vaccine composition.
Area of Science:
- Virology and Immunology
- Public Health and Epidemiology
- Vaccinology
Background:
- The continuous evolution of SARS-CoV-2, particularly JN.1 lineage descendants, necessitates ongoing evaluation of COVID-19 vaccine effectiveness (VE).
- Understanding VE against severe outcomes is critical for informing and adapting public vaccination strategies in response to emerging viral variants.
Purpose of the Study:
- To estimate the VE of 2024-2025 COVID-19 vaccines against COVID-19-associated hospitalization and severe in-hospital outcomes.
- To analyze VE stratified by time since vaccination, specific JN.1 descendant lineages (KP.3.1.1, XEC, LP.8.1), and immune-evasive spike protein mutations.
Main Methods:
- A multicenter, test-negative, case-control study involving adult patients hospitalized with COVID-19-like illness between September 2024 and April 2025.
- Case patients tested positive for SARS-CoV-2, while control patients tested negative.
- Logistic regression was employed to calculate VE as (1 - adjusted odds ratio) × 100%, adjusting for relevant covariates.
Main Results:
- Overall VE against COVID-19-associated hospitalization was 40%, with sustained protection up to 179 days post-vaccination.
- VE against severe outcomes, including invasive mechanical ventilation or death, was notably high at 79%.
- Effectiveness varied by lineage, with VE against KP.3.1.1 hospitalization at 49%, XEC at 34%, and LP.8.1 at 24%.
Conclusions:
- The 2024-2025 COVID-19 vaccines provided significant protection against hospitalization and severe outcomes during the circulation of JN.1 descendant lineages.
- VE varied across different SARS-CoV-2 lineages and was influenced by spike protein mutations, highlighting the need for lineage-specific analysis.
- Continued monitoring and stratification of VE by viral lineage and mutations are essential for optimizing COVID-19 vaccine composition and recommendations.
Importance:
As SARS-CoV-2 JN.1 lineage descendants continue to evolve, evaluating COVID-19 vaccine effectiveness (VE) against severe COVID-19 remains important to guide vaccination strategies.
Objective:
To estimate the VE of the 2024-2025 COVID-19 vaccines against COVID-19-associated hospitalization and severe in-hospital outcomes overall and by time since dose (7-89, 90-179, and ≥180 days), JN.1 descendant lineage (KP.3.1.1, XEC, LP.8.1), and spike protein mutations associated with immune evasion.
Design, Setting, And Participants:
This multicenter, test-negative, case-control study conducted by the Investigating Respiratory Viruses in the Acutely Ill Network included adult patients (aged ≥18 years) hospitalized between September 1, 2024, and April 30, 2025, at 26 hospitals in 20 US states. Case patients presented with COVID-19-like illness and positive SARS-CoV-2 nucleic acid or antigen test results; control patients had COVID-19-like illness but tested negative for SARS-CoV-2.
Exposure:
Receipt of a 2024-2025 COVID-19 vaccine at least 7 days before illness onset.
Main Outcomes And Measures:
Main outcomes were COVID-19-associated hospitalization and severe in-hospital outcomes (supplemental oxygen therapy, acute respiratory failure, intensive care unit admission, and invasive mechanical ventilation or death). Logistic regression was used to estimate the odds of vaccination in case and control patients, adjusting for demographics, clinical characteristics, and enrollment region. The VE was estimated as (1 - adjusted odds ratio) × 100%.
Results:
A total of 8493 patients (median [IQR] age, 66 [54-76] years; 4338 female [51.1%]), including 1888 case patients with COVID-19 (among whom 951 [50.4%] had successful whole-genome sequencing, including 348 [36.6%] with KP.3.1.1, 218 [22.9%] with XEC, and 134 [14.1%] with LP.8.1 infections) and 6605 control patients were enrolled. Vaccine effectiveness against COVID-19-associated hospitalization was 40% (95% CI, 27%-51%), and protection was sustained through 90 to 179 days after vaccination. Vaccine effectiveness was higher against the most severe outcome of invasive mechanical ventilation or death at 79% (95% CI, 55%-92%). It was 49% (95% CI, 25%-67%) against hospitalization with KP.3.1.1, 34% (95% CI, 4%-56%) against XEC, and 24% (95% CI, -19% to 53%) against LP.8.1, with increasing median time since dose receipt among vaccinated case patients due to sequential circulation patterns (60, 89, and 141 days, respectively). The VE was similar against lineages with spike protein S31 deletion (41% [95% CI, 22%-56%]) and T22N and F59S substitutions (37% [95% CI, 9%-57%]).
Conclusions And Relevance:
In this multicenter, case-control analysis of VE, 2024-2025 COVID-19 vaccines may have provided protection against hospitalizations and severe in-hospital outcomes as multiple JN.1 descendant lineages circulated. Monitoring COVID-19 VE, including stratifying by SARS-CoV-2 lineage and spike protein mutations, remains important to guide COVID-19 vaccine composition and recommendations.
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