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Dynamics of SARS-CoV-2 VOC neutralization and novel mAb reveal protection against Omicron
Linhui Hao; Tien-Ying Hsiang; Ronit R. Dalmat; Renee Ireton; Jennifer Morton; Caleb Stokes; Jason Netland; Malika Hale; Chris Thouvenel; Anna Wald; Nicholas M Franko; Kristen Huden; Helen Chu; Alex Greninger; Sasha Tilles; Lynn K. Barrett; Wesley C. Van Voorhis; Jennifer Munt; Trevor Scobey; Ralph S. Baric; David Rawlings; Marion Pepper; Paul K. Drain; Michael Gale Jr..
Affiliation
  • Linhui Hao; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Tien-Ying Hsiang; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Ronit R. Dalmat; International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA
  • Renee Ireton; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Jennifer Morton; International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA
  • Caleb Stokes; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Jason Netland; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Malika Hale; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Chris Thouvenel; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Anna Wald; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA
  • Nicholas M Franko; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA
  • Kristen Huden; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA
  • Helen Chu; Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA
  • Alex Greninger; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA
  • Sasha Tilles; Center for Emerging & Re-emerging Infectious Diseases, University of Washington, Seattle, WA
  • Lynn K. Barrett; Center for Emerging & Re-emerging Infectious Diseases, University of Washington, Seattle, WA
  • Wesley C. Van Voorhis; Center for Emerging & Re-emerging Infectious Diseases, University of Washington, Seattle, WA
  • Jennifer Munt; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill NC
  • Trevor Scobey; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill NC
  • Ralph S. Baric; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill NC
  • David Rawlings; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Marion Pepper; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
  • Paul K. Drain; International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA
  • Michael Gale Jr.; Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA
Preprint in English | medRxiv | ID: ppmedrxiv-22278720
ABSTRACT
To evaluate SARS-CoV-2 variants we isolated SARS-CoV-2 temporally during the pandemic starting with first appearance of virus in the Western hemisphere near Seattle, WA, USA, and isolated each known major variant class, revealing the dynamics of emergence and complete take-over of all new cases by current Omicron variants. We assessed virus neutralization in a first-ever full comparison across variants and evaluated a novel monoclonal antibody (Mab). We found that convalescence greater than 5-months provides little-to-no protection against SARS-CoV-2 variants, vaccination enhances immunity against variants with the exception of Omicron BA.1, and paired testing of vaccine sera against ancestral virus compared to Omicron BA.1 shows that 3-dose vaccine regimen provides over 50-fold enhanced protection against Omicron BA.1 compared to a 2-dose regimen. We also reveal a novel Mab that effectively neutralizes Omicron BA.1 and BA.2 variants over clinically-approved Mabs. Our observations underscore the need for continued vaccination efforts, with innovation for vaccine and Mab improvement, for protection against variants of SARS-CoV-2. SummaryWe isolated SARS-CoV-2 temporally starting with emergence of virus in the Western hemisphere. Neutralization analyses across all variant lineages show that vaccine-boost regimen provides protection against Omicron BA.1. We reveal a Mab that protects against Omicron BA.1 and BA.2 variants.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
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