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Effectiveness of a bivalent mRNA vaccine dose against symptomatic SARS-CoV-2 infection among U.S. Healthcare personnel, September 2022-May 2023.
Plumb, Ian D; Briggs Hagen, Melissa; Wiegand, Ryan; Dumyati, Ghinwa; Myers, Christopher; Harland, Karisa K; Krishnadasan, Anusha; James Gist, Jade; Abedi, Glen; Fleming-Dutra, Katherine E; Chea, Nora; Lee, Jane E; Kellogg, Melissa; Edmundson, Alexandra; Britton, Amber; Wilson, Lucy E; Lovett, Sara A; Ocampo, Valerie; Markus, Tiffanie M; Smithline, Howard A; Hou, Peter C; Lee, Lilly C; Mower, William; Rwamwejo, Fernand; Steele, Mark T; Lim, Stephen C; Schrading, Walter A; Chinnock, Brian; Beiser, David G; Faine, Brett; Haran, John P; Nandi, Utsav; Chipman, Anne K; LoVecchio, Frank; Eucker, Stephanie; Femling, Jon; Fuller, Matthew; Rothman, Richard E; Curlin, Marcel E; Talan, David A; Mohr, Nicholas M.
Afiliação
  • Plumb ID; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA. Electronic address: iplumb@cdc.gov.
  • Briggs Hagen M; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA.
  • Wiegand R; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA.
  • Dumyati G; University of Rochester Medical Center, Rochester, NY, USA.
  • Myers C; University of Rochester Medical Center, Rochester, NY, USA.
  • Harland KK; University of Iowa, Iowa City, IA, USA.
  • Krishnadasan A; Olive View- UCLA Education and Research Institute, CA, USA.
  • James Gist J; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA.
  • Abedi G; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA.
  • Fleming-Dutra KE; National Center for Immunizations and Respiratory Diseases, Centers for Disease Control & Prevention, Atlanta, GA, USA.
  • Chea N; National Center for Emerging and Zoonotic Diseases, Centers for Disease Control & Prevention, USA.
  • Lee JE; California Emerging Infections Program, Oakland, CA, USA.
  • Kellogg M; Colorado Department of Public Health & Environment, CO, USA.
  • Edmundson A; Connecticut Emerging Infections Program, Yale School of Public Health, CT, USA.
  • Britton A; Georgia Emerging Infections Program and Emory University School of Medicine, Atlanta, GA, USA.
  • Wilson LE; Maryland Emerging Infections Program, Maryland Department of Health and University of Maryland, Baltimore, MD, USA.
  • Lovett SA; Minnesota Department of Health, MN, USA.
  • Ocampo V; Public Health Division, Oregon Health Authority, OR, USA.
  • Markus TM; Vanderbilt University Medical Center, Nashville, TN, USA.
  • Smithline HA; Baystate Medical Center, Springfield, MA, USA.
  • Hou PC; Brigham and Women's Hospital, Boston, MA, USA.
  • Lee LC; Jackson Memorial Hospital, Miami, FL, USA.
  • Mower W; David Geffen School of Medicine, UCLA, CA, USA.
  • Rwamwejo F; Thomas Jefferson University Hospital, Philadelphia, PA, USA.
  • Steele MT; University of Missouri-Kansas City, Kansas City, MO, USA.
  • Lim SC; University Medical Center New Orleans, LSU Health Sciences Center, New Orleans, LA, USA.
  • Schrading WA; University of Alabama at Birmingham, Birmingham, AL, USA.
  • Chinnock B; University of California San Francisco, Fresno, CA, USA.
  • Beiser DG; University of Chicago, Chicago, IL, USA.
  • Faine B; University of Iowa, Iowa City, IA, USA.
  • Haran JP; University of Massachusetts Chan Medical School, Worcester, MA, USA.
  • Nandi U; University of Mississippi Medical Center, Jackson, MS, USA.
  • Chipman AK; University of Washington, Seattle, WA, USA.
  • LoVecchio F; Valleywise Health Medical Center, Phoenix, AZ, USA.
  • Eucker S; Duke University School of Medicine, NC, USA.
  • Femling J; University of New Mexico Health Science Center, USA.
  • Fuller M; University of Utah School of Medicine, USA.
  • Rothman RE; Department of Emergency Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Curlin ME; Oregon Health and Sciences University, USA.
  • Talan DA; David Geffen School of Medicine, UCLA, CA, USA.
  • Mohr NM; University of Iowa, Iowa City, IA, USA.
Vaccine ; 42(10): 2543-2552, 2024 Apr 11.
Article em En | MEDLINE | ID: mdl-37973512
ABSTRACT

BACKGROUND:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans / Newborn Idioma: En Revista: Vaccine Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Humans / Newborn Idioma: En Revista: Vaccine Ano de publicação: 2024 Tipo de documento: Article