Effectiveness of a bivalent mRNA vaccine dose against symptomatic SARS-CoV-2 infection among U.S. Healthcare personnel, September 2022–May 2023

dc.contributor.authorPlumb, Ian D.
dc.contributor.authorBriggs Hagen, Melissa
dc.contributor.authorWiegand, Ryan
dc.contributor.authorDumyati, Ghinwa
dc.contributor.authorMyers, Christopher
dc.contributor.authorHarland, Karisa K.
dc.contributor.authorKrishnadasan, Anusha
dc.contributor.authorJames Gist, Jade
dc.contributor.authorAbedi, Glen
dc.contributor.authorFleming-Dutra, Katherine E.
dc.contributor.authorChea, Nora
dc.contributor.authorLee, Jane E.
dc.contributor.authorKellogg, Melissa
dc.contributor.authorEdmundson, Alexandra
dc.contributor.authorBritton, Amber
dc.contributor.authorWilson, Lucy
dc.contributor.authorLovett, Sara A.
dc.contributor.authorOcampo, Valerie
dc.contributor.authorMarkus, Tiffanie M.
dc.contributor.authorSmithline, Howard A.
dc.contributor.authorHou, Peter C.
dc.contributor.authorLee, Lilly C.
dc.contributor.authorMower, William
dc.contributor.authorRwamwejo, Fernand
dc.contributor.authorSteele, Mark T.
dc.contributor.authorLim, Stephen C.
dc.contributor.authorSchrading, Walter A.
dc.contributor.authorChinnock, Brian
dc.contributor.authorBeiser, David G.
dc.contributor.authorFaine, Brett
dc.contributor.authorHaran, John P.
dc.contributor.authorNandi, Utsav
dc.contributor.authorChipman, Anne K.
dc.contributor.authorLoVecchio, Frank
dc.contributor.authorEucker, Stephanie
dc.contributor.authorFemling, Jon
dc.contributor.authorFuller, Matthew
dc.contributor.authorRothman, Richard E.
dc.contributor.authorCurlin, Marcel E.
dc.contributor.authorTalan, David A.
dc.contributor.authorMohr, Nicholas M.
dc.date.accessioned2024-06-11T13:30:02Z
dc.date.available2024-06-11T13:30:02Z
dc.date.issued2024-04-11
dc.description.abstractBackground: Bivalent mRNA vaccines were recommended since September 2022. However, coverage with a recent vaccine dose has been limited, and there are few robust estimates of bivalent VE against symptomatic SARS-CoV-2 infection (COVID-19). We estimated VE of a bivalent mRNA vaccine dose against COVID-19 among eligible U.S. healthcare personnel who had previously received monovalent mRNA vaccine doses. Methods: We conducted a case-control study in 22 U.S. states, and enrolled healthcare personnel with COVID-19 (case-participants) or without COVID-19 (control-participants) during September 2022–May 2023. Participants were considered eligible for a bivalent mRNA dose if they had received 2–4 monovalent (ancestral-strain) mRNA vaccine doses, and were >=67 days after the most recent vaccine dose. We estimated VE of a bivalent mRNA dose using conditional logistic regression, accounting for matching by region and four-week calendar period. We adjusted estimates for age group, sex, race and ethnicity, educational level, underlying health conditions, community COVID-19 exposure, prior SARS-CoV-2 infection, and days since the last monovalent mRNA dose. Results: Among 3,647 healthcare personnel, 1,528 were included as case-participants and 2,119 as control-participants. Participants received their last monovalent mRNA dose a median of 404 days previously; 1,234 (33.8%) also received a bivalent mRNA dose a median of 93 days previously. Overall, VE of a bivalent dose was 34.1% (95% CI, 22.6%–43.9%) against COVID-19 and was similar by product, days since last monovalent dose, number of prior doses, age group, and presence of underlying health conditions. However, VE declined from 54.8% (95% CI, 40.7%–65.6%) after 7–59 days to 21.6% (95% CI 5.6%–34.9%) after >=60 days. Conclusions: Bivalent mRNA COVID-19 vaccines initially conferred approximately 55% protection against COVID-19 among U.S. healthcare personnel. However, protection waned after two months. These findings indicate moderate initial protection against symptomatic SARS-CoV-2 infection by remaining up-to-date with COVID-19 vaccines.
dc.description.sponsorshipThis project was funded by the Centers for Disease Control and Prevention (CDC) (U01CK000480). The project is additionally supported by the Institute for Clinical and Translational Science at the University of Iowa through a grant from the National Center for Advancing Translational Sciences at the National Institutes of Health (UL1TR002537).
dc.description.urihttps://www.sciencedirect.com/science/article/pii/S0264410X23012872
dc.format.extent10 pages
dc.genrejournal articles
dc.identifierdoi:10.13016/m2gi5a-2l6r
dc.identifier.citationPlumb, Ian D., Melissa Briggs Hagen, Ryan Wiegand, Ghinwa Dumyati, Christopher Myers, Karisa K. Harland, Anusha Krishnadasan, et al. “Effectiveness of a Bivalent MRNA Vaccine Dose against Symptomatic SARS-CoV-2 Infection among U.S. Healthcare Personnel, September 2022–May 2023.” Vaccine 42, no. 10 (April 11, 2024): 2543–52. https://doi.org/10.1016/j.vaccine.2023.10.072.
dc.identifier.urihttps://doi.org/10.1016/j.vaccine.2023.10.072
dc.identifier.urihttp://hdl.handle.net/11603/34547
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Emergency and Distaster Health Systems
dc.rightsThis work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
dc.rightsPublic Domain
dc.rights.urihttps://creativecommons.org/publicdomain/mark/1.0/
dc.subjectBivalent
dc.subjectCOVID-19
dc.subjectCOVID-19 vaccines
dc.subjectHealthcare personnel
dc.subjectmRNA vaccines
dc.subjectSARS-CoV-2
dc.subjectVaccine effectiveness
dc.titleEffectiveness of a bivalent mRNA vaccine dose against symptomatic SARS-CoV-2 infection among U.S. Healthcare personnel, September 2022–May 2023
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0003-0092-1750

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
1-s2.0-S0264410X23012872-main.pdf
Size:
1.01 MB
Format:
Adobe Portable Document Format