Prevention and Attenuation of Covid-19 with the BNT162b2 and mRNA-1273 Vaccines
Author
Thompson, M.G.Burgess, J.L.
Naleway, A.L.
Tyner, H.
Yoon, S.K.
Meece, J.
Olsho, L.E.W.
Caban-Martinez, A.J.
Fowlkes, A.L.
Lutrick, K.
Groom, H.C.
Dunnigan, K.
Odean, M.J.
Hegmann, K.
Stefanski, E.
Edwards, L.J.
Schaefer-Solle, N.
Grant, L.
Ellingson, K.
Kuntz, J.L.
Zunie, T.
Thiese, M.S.
Ivacic, L.
Wesley, M.G.
Lamberte, J.M.
Sun, X.
Smith, M.E.
Phillips, A.L.
Groover, K.D.
Yoo, Y.M.
Gerald, J.
Brown, R.T.
Herring, M.K.
Joseph, G.
Beitel, S.
Morrill, T.C.
Mak, J.
Rivers, P.
Poe, B.P.
Lynch, B.
Zhou, Y.
Zhang, J.
Kelleher, A.
Li, Y.
Dickerson, M.
Hanson, E.
Guenther, K.
Tong, S.
Bateman, A.
Reisdorf, E.
Barnes, J.
Azziz-Baumgartner, E.
Hunt, D.R.
Arvay, M.L.
Kutty, P.
Fry, A.M.
Gaglani, M.
Affiliation
Mel and Enid Zuckerman College of Public Health, University of ArizonaIssue Date
2021
Metadata
Show full item recordPublisher
Massachussetts Medical SocietyCitation
Thompson, M. G., Burgess, J. L., Naleway, A. L., Tyner, H., Yoon, S. K., Meece, J., Olsho, L. E. W., Caban-Martinez, A. J., Fowlkes, A. L., Lutrick, K., Groom, H. C., Dunnigan, K., Odean, M. J., Hegmann, K., Stefanski, E., Edwards, L. J., Schaefer-Solle, N., Grant, L., Ellingson, K., … Gaglani, M. (2021). Prevention and Attenuation of Covid-19 with the BNT162b2 and mRNA-1273 Vaccines. New England Journal of Medicine, 385(4), 320–329.Journal
New England Journal of MedicineRights
Copyright © 2021 Massachusetts Medical Society.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
BACKGROUND Information is limited regarding the effectiveness of the two-dose messenger RNA (mRNA) vaccines BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna) in preventing infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and in attenuating coronavirus disease 2019 (Covid-19) when administered in realworld conditions. METHODS We conducted a prospective cohort study involving 3975 health care personnel, first responders, and other essential and frontline workers. From December 14, 2020, to April 10, 2021, the participants completed weekly SARS-CoV-2 testing by providing mid-turbinate nasal swabs for qualitative and quantitative reverse-transcriptase-polymerase-chain-reaction (RT-PCR) analysis. The formula for calculating vaccine effectiveness was 100% × (1 - hazard ratio for SARS-CoV-2 infection in vaccinated vs. unvaccinated participants), with adjustments for the propensity to be vaccinated, study site, occupation, and local viral circulation. RESULTS SARS-CoV-2 was detected in 204 participants (5%), of whom 5 were fully vaccinated (≥14 days after dose 2), 11 partially vaccinated (=14 days after dose 1 and <14 days after dose 2), and 156 unvaccinated; the 32 participants with indeterminate vaccination status (<14 days after dose 1) were excluded. Adjusted vaccine effectiveness was 91% (95% confidence interval [CI], 76 to 97) with full vaccination and 81% (95% CI, 64 to 90) with partial vaccination. Among participants with SARS-CoV-2 infection, the mean viral RNA load was 40% lower (95% CI, 16 to 57) in partially or fully vaccinated participants than in unvaccinated participants. In addition, the risk of febrile symptoms was 58% lower (relative risk, 0.42; 95% CI, 0.18 to 0.98) and the duration of illness was shorter, with 2.3 fewer days spent sick in bed (95% CI, 0.8 to 3.7). CONCLUSIONS Authorized mRNA vaccines were highly effective among working-age adults in preventing SARS-CoV-2 infection when administered in real-world conditions, and the vaccines attenuated the viral RNA load, risk of febrile symptoms, and duration of illness among those who had breakthrough infection despite vaccination. (Funded by the National Center for Immunization and Respiratory Diseases and the Centers for Disease Control and Prevention.) Copyright © 2021 Massachusetts Medical Society.Note
No embargo COVID-19ISSN
0028-4793PubMed ID
34192428Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1056/NEJMoa2107058
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