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Abstract
Studies of comparative mRNA booster effectiveness among high-risk populations can inform mRNA booster-specific guidelines. The study emulated a target trial of COVID-19 vaccinated U.S. Veterans who received three doses of either mRNA-1273 or BNT162b2 vaccines. Participants were followed for up to 32 weeks between July 1, 2021 to May 30, 2022. Non-overlapping populations were average and high risk; high-risk sub-groups were age ≥65 years, high-risk co-morbid conditions, and immunocompromising conditions. Of 1,703,189 participants, 10.9 per 10,000 persons died or were hospitalized with COVID-19 pneumonia over 32 weeks (95% CI: 10.2, 11.8). Although relative risks of death or hospitalization with COVID-19 pneumonia were similar across at-risk groups, absolute risk varied when comparing three doses of BNT162b2 with mRNA-1273 (BNT162b2 minus mRNA-1273) between average-risk and high-risk populations, confirmed by the presence of additive interaction. The risk difference of death or hospitalization with COVID-19 pneumonia for high-risk populations was 2.2 (0.9, 3.6). Effects were not modified by predominant viral variant. In this work, the risk of death or hospitalization with COVID-19 pneumonia over 32 weeks was lower among high-risk populations who received three doses of mRNA-1273 vaccine instead of BNT162b2 vaccine; no difference was found among the average-risk population and age >65 sub-group.
mRNA boosters have been shown to be effective against severe COVID-19 illness. In this work, the authors show that in high-risk populations, three doses of mRNA-1273 vaccine instead of BNT162b2 vaccine conferred a small benefit against death or hospitalization with COVID-19 pneumonia.
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1 San Francisco VA Medical Center, San Francisco, USA (GRID:grid.410372.3) (ISNI:0000 0004 0419 2775); University of California, San Francisco (UCSF), Department of Medicine, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); UCSF, Department of Epidemiology and Biostatistics, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); UCSF, F.I. Proctor Foundation, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
2 San Francisco VA Medical Center, San Francisco, USA (GRID:grid.410372.3) (ISNI:0000 0004 0419 2775)
3 UCSF, Department of Epidemiology and Biostatistics, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
4 San Francisco VA Medical Center, San Francisco, USA (GRID:grid.410372.3) (ISNI:0000 0004 0419 2775); University of California, San Francisco (UCSF), Department of Medicine, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
5 Richard L. Roudebush VA Medical Center, Department of Veterans Affairs (VA) Health Services and Development (HSR&D) Center for Health Information and Communication (CHIC) and the Department of Medicine, Indianapolis, USA (GRID:grid.280828.8) (ISNI:0000 0000 9681 3540); Veterans Affairs Medical Center, Indianapolis, USA (GRID:grid.280828.8)
6 Institute for Clinical Evaluative Sciences, Toronto, Canada (GRID:grid.418647.8) (ISNI:0000 0000 8849 1617)
7 Richard L. Roudebush VA Medical Center, Department of Veterans Affairs (VA) Health Services and Development (HSR&D) Center for Health Information and Communication (CHIC) and the Department of Medicine, Indianapolis, USA (GRID:grid.280828.8) (ISNI:0000 0000 9681 3540); Indiana University School of Medicine, Department of Medicine, Indianapolis, USA (GRID:grid.257413.6) (ISNI:0000 0001 2287 3919); Regenstrief Institute, Indianapolis, USA (GRID:grid.448342.d) (ISNI:0000 0001 2287 2027)