Your browser doesn't support javascript.
loading
SARS-CoV-2 Variant Vaccine Boosters Trial: Preliminary Analyses
Angela R Branche; Nadine G Rouphael; David D Diemert; Ann R Falsey; Cecilia Losada; Lindsey R Baden; Sharon E Frey; Jennifer A Whitaker; Susan J Little; Evan J Anderson; Emmanuel B Walter; Richard M Novak; Richard Rupp; Lisa A Jackson; Tara M Babu; Angelica C Kottkamp; Anne F Luetkemeyer; Lilly C Immergluck; Rachel M Presti; Martin Backer; Patricia L Winokur; Siham M Mahgoub; Paul A Goepfert; Dahlene N Fusco; Elissa Malkin; Jeffrey M Bethony; Edward E Walsh; Daniel S Graciaa; Hady Samaha; Amy C Sherman; Stephen R Walsh; getahun Abate; Zacharoula Oikonomopoulou; Hana M El Sahly; Thomas CS Martin; Christina A. Rostad; Michael Smith; Benjamin G Ladner; Laura Porterfield; Maya Dunstan; Anna Wald; Tamia Davis; Robert L Atmar; Mark J Mulligan; Kirsten E Lyke; Christine M Posavad; Megan A Meagher; David S Stephens; Kathleen M Neuzil; Kuleni Abebe; Heather Hill; Jim Albert; Teri C Lewis; Lisa A Giebeig; Amanda Eaton; Antonia Netzl; Samuel Hedley Wilks; Sina Tureli; Mamodikoe Mahkene; Sonja Crandon; Marina Lee; Seema U Nayak; David C Montefiori; Mat Matkowski; Derek J Smith; Paul C Roberts; John H Beigel.
Afiliação
  • Angela R Branche; University of Rochester
  • Nadine G Rouphael; Emory University
  • David D Diemert; George Washington University
  • Ann R Falsey; University of Rochester
  • Cecilia Losada; Emory University
  • Lindsey R Baden; Brigham and Women's Hospital, Harvard Medical School
  • Sharon E Frey; Saint Louis University
  • Jennifer A Whitaker; Baylor College of Medicine
  • Susan J Little; University of California San Diego
  • Evan J Anderson; Emory University
  • Emmanuel B Walter; Duke University
  • Richard M Novak; University of Illinois at Chicago
  • Richard Rupp; University of Texas Medical Branch
  • Lisa A Jackson; Kaiser Permanente Washington Health
  • Tara M Babu; University of Washington
  • Angelica C Kottkamp; NYU Langone Manhattan
  • Anne F Luetkemeyer; Zuckerberg San Francisco General Hospital UCSF
  • Lilly C Immergluck; Moorehouse School of Medicine
  • Rachel M Presti; Washington University
  • Martin Backer; NYU Langone Long Island
  • Patricia L Winokur; University of Iowa
  • Siham M Mahgoub; Howard University Hospital
  • Paul A Goepfert; University of Alabama at Birmingham
  • Dahlene N Fusco; Tulane University
  • Elissa Malkin; George Washington University
  • Jeffrey M Bethony; George Washington University
  • Edward E Walsh; University of Rochester
  • Daniel S Graciaa; Emory University
  • Hady Samaha; Emory University
  • Amy C Sherman; Brigham and Women's Hospital, Harvard Medical School
  • Stephen R Walsh; Brigham and Women's Hospital, Harvard Medical School
  • getahun Abate; Saint Louis University
  • Zacharoula Oikonomopoulou; Saint Louis University
  • Hana M El Sahly; Baylor College of Medicine
  • Thomas CS Martin; University of California San Diego
  • Christina A. Rostad; Emory University School of Medicine
  • Michael Smith; Duke University School of Medicine
  • Benjamin G Ladner; University of Illinois at Chicago
  • Laura Porterfield; University of Texas Medical Branch
  • Maya Dunstan; Kaiser Permanente Washington Health
  • Anna Wald; University of Washington
  • Tamia Davis; NYu Langone Manhattan
  • Robert L Atmar; Baylor College of Medicine
  • Mark J Mulligan; New York University Grossman School of Medicine
  • Kirsten E Lyke; University of Maryland, Baltimore
  • Christine M Posavad; University of Washington, Fred Hutchinson Cancer Center
  • Megan A Meagher; University of Washington, Fred Hutchinson Cancer Center
  • David S Stephens; Emory University
  • Kathleen M Neuzil; University of Maryland School of Medicine
  • Kuleni Abebe; FHI360
  • Heather Hill; The Emmes Company
  • Jim Albert; The Emmes Company
  • Teri C Lewis; Frederick National Laboratory for Cancer Research
  • Lisa A Giebeig; Frederick National Laboratory for Cancer Research
  • Amanda Eaton; Duke University School of Medicine
  • Antonia Netzl; University of Cambridge
  • Samuel Hedley Wilks; University of Cambridge
  • Sina Tureli; University of Cambridge
  • Mamodikoe Mahkene; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Sonja Crandon; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Marina Lee; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • Seema U Nayak; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • David C Montefiori; Duke University School of Medicine
  • Mat Matkowski; The Emmes Company
  • Derek J Smith; Cambridge University
  • Paul C Roberts; National Institute of Allergy and Infectious Diseases, National Institutes of Health
  • John H Beigel; National Institute of Allergy and Infectious Diseases, National Institutes of Health
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22277336
ABSTRACT
BackgroundProtection from SARS-CoV-2 vaccines wanes over time and is compounded by emerging variants including Omicron subvariants. This study evaluated safety and immunogenicity of SARS-CoV-2 variant vaccines. MethodsThis phase 2 open-label, randomized trial enrolled healthy adults previously vaccinated with a SARS-CoV-2 primary series and a single boost. Eligible participants were randomized to one of six Moderna COVID19 mRNA vaccine arms (50{micro}g dose) Prototype (mRNA-1273), Omicron BA.1+Beta (1 or 2 doses), Omicron BA.1+Delta, Omicron BA.1 monovalent, and Omicron BA.1+Prototype. Neutralization antibody titers (ID50) were assessed for D614G, Delta, Beta and Omicron BA.1 variants and Omicron BA.2.12.1 and BA.4/BA.5 subvariants 15 days after vaccination. ResultsFrom March 30 to May 6, 2022, 597 participants were randomized and vaccinated. Median age was 53 years, and 20% had a prior SARS-CoV-2 infection. All vaccines were safe and well-tolerated. Day 15 geometric mean titers (GMT) against D614G were similar across arms and ages, and higher with prior infection. For uninfected participants, Day 15 Omicron BA.1 GMTs were similar across Omicron-containing vaccine arms (3724-4561) and higher than Prototype (1,997 [95%CI1,482-2,692]). The Omicron BA.1 monovalent and Omicron BA.1+Prototype vaccines induced a geometric mean ratio (GMR) to Prototype for Omicron BA.1 of 2.03 (97.5%CI1.37-3.00) and 1.56 (97.5%CI1.06-2.31), respectively. A subset of samples from uninfected participants in four arms were also tested in a different laboratory at Day 15 for neutralizing antibody titers to D614G and Omicron subvariants BA.1, BA.2.12.2 and BA.4/BA.5. Omicron BA.4/BA.5 GMTs were approximately one third BA.1 GMTs (Prototype 517 [95%CI324-826] vs. 1503 [95%CI949-2381]; Omicron BA.1+Beta 628 [95%CI367-1,074] vs. 2125 [95%CI1139-3965]; Omicron BA.1+Delta 765 [95%CI443-1,322] vs. 2242 [95%CI1218-4128] and Omicron BA.1+Prototype 635 [95%CI447-903] vs. 1972 [95%CI1337-2907). ConclusionsHigher Omicron BA.1 titers were observed with Omicron-containing vaccines compared to Prototype vaccine and titers against Omicron BA.4/BA.5 were lower than against BA.1 for all candidate vaccines. Clinicaltrials.govNCT05289037
Licença
cc_no
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint