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Booster of mRNA-1273 Vaccine Reduces SARS-CoV-2 Omicron Escape from Neutralizing Antibodies
Nicole Doria-Rose; Xiaoying Shen; Stephen D Schmidt; Sijy O'Dell; Charlene McDanal; Wenhong Feng; Jin Tong; Amanda Eaton; Maha Maglinao; Haili Tang; Kelly E Manning; Venkata-Viswanadh Edara; Linlin Lai; Madison Ellis; Kathryn Moore; Katharine Floyd; Stephanie L Foster; Robert L Atmar; Kirsten E Lyke; Tongqing Zhou; Lingshu Wang; yi Zhang; Martin R Gaudinski; Walker P Black; Ingelise Gordon; Mercy Guech; Julie E Ledgerwood; John N Misasi; Alicia Widge; Paul C Roberts; John Beigel; Bette Korber; Rolando Pajon; John R Mascola; Mehul S Suthar; David C Montefiori.
Affiliation
  • Nicole Doria-Rose; National Institutes of Health
  • Xiaoying Shen; DUKE UNIVERSITY MEDICAL CENTER
  • Stephen D Schmidt; National Institutes of Health
  • Sijy O'Dell; National Institutes of Health
  • Charlene McDanal; Duke University Medical Center
  • Wenhong Feng; Duke University Medical Center
  • Jin Tong; Duke University Medical Center
  • Amanda Eaton; Duke University Medical Center
  • Maha Maglinao; Moderna, Inc.
  • Haili Tang; Duke University Medical Center
  • Kelly E Manning; Emory University
  • Venkata-Viswanadh Edara; Emory University
  • Linlin Lai; Emory University
  • Madison Ellis; Emory University
  • Kathryn Moore; Emory University
  • Katharine Floyd; Emory University
  • Stephanie L Foster; Emory University
  • Robert L Atmar; Baylor College of Medicine
  • Kirsten E Lyke; University of Maryland School of Medicine
  • Tongqing Zhou; National Institutes of Health
  • Lingshu Wang; National Institutes of Health
  • yi Zhang; National Institutes of Health
  • Martin R Gaudinski; National Institutes of Health
  • Walker P Black; National Institutes of Health
  • Ingelise Gordon; National Institutes of Health
  • Mercy Guech; National Institutes of Health
  • Julie E Ledgerwood; National Institutes of Health
  • John N Misasi; National Institutes of Health
  • Alicia Widge; National Institutes of Health
  • Paul C Roberts; National Institutes of Health
  • John Beigel; National Institutes of Health
  • Bette Korber; Los Alamos National Laboratory
  • Rolando Pajon; Moderna Inc.
  • John R Mascola; National Institutes of Health
  • Mehul S Suthar; Emory University
  • David C Montefiori; Duke University Medical Center
Preprint in English | medRxiv | ID: ppmedrxiv-21267805
ABSTRACT
The Omicron variant of SARS-CoV-2 is raising concerns because of its increased transmissibility and potential for reduced susceptibility to antibody neutralization. To assess the potential risk of this variant to existing vaccines, serum samples from mRNA-1273 vaccine recipients were tested for neutralizing activity against Omicron and compared to neutralization titers against D614G and Beta in live virus and pseudovirus assays. Omicron was 41-84-fold less sensitive to neutralization than D614G and 5.3-7.4-fold less sensitive than Beta when assayed with serum samples obtained 4 weeks after 2 standard inoculations with 100 {micro}g mRNA-1273. A 50 {micro}g boost increased Omicron neutralization titers and may substantially reduce the risk of symptomatic vaccine breakthrough infections.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Prognostic study Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Prognostic study Language: English Year: 2021 Document type: Preprint
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