Dynamics of SARS-CoV-2 VOC Neutralization and Novel mAb Reveal Protection against Omicron

Author:

Hao Linhui12,Hsiang Tien-Ying12,Dalmat Ronit R.34ORCID,Ireton Renee12ORCID,Morton Jennifer F.34,Stokes Caleb125,Netland Jason1,Hale Malika1ORCID,Thouvenel Chris1,Wald Anna4678ORCID,Franko Nicholas M.6ORCID,Huden Kristen6,Chu Helen Y.6,Sigal Alex91011,Greninger Alex L.12ORCID,Tilles Sasha26ORCID,Barrett Lynn K.26,Van Voorhis Wesley C.26,Munt Jennifer13,Scobey Trevor13,Baric Ralph S.13ORCID,Rawlings David J.1,Pepper Marion1,Drain Paul K.346ORCID,Gale Michael12ORCID

Affiliation:

1. Department of Immunology, Center for Innate Immunity and Immune Disease, University of Washington, Seattle, WA 98109, USA

2. Center for Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA 98109, USA

3. International Clinical Research Center, Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA 98104, USA

4. Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA 98195, USA

5. Department of Pediatrics, School of Medicine, University of Washington, Seattle, WA 98195, USA

6. Division of Allergy and Infectious Diseases, Department of Medicine, School of Medicine, University of Washington, Seattle, WA 98195, USA

7. Allergy and Infectious Diseases Division, Laboratory Medicine & Pathology, & Epidemiology, University of Washington, Seattle, WA 98195, USA

8. Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA 98109, USA

9. Africa Health Research Institute, Durban 4001, South Africa

10. School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Mayville 4058, South Africa

11. Centre for the AIDS Program of Research in South Africa, Congella 4013, South Africa

12. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98195, USA

13. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC 27695, USA

Abstract

New variants of SARS-CoV-2 continue to emerge and evade immunity. We isolated SARS-CoV-2 temporally across the pandemic starting with the first emergence of the virus in the western hemisphere and evaluated the immune escape among variants. A clinic-to-lab viral isolation and characterization pipeline was established to rapidly isolate, sequence, and characterize SARS-CoV-2 variants. A virus neutralization assay was applied to quantitate humoral immunity from infection and/or vaccination. A panel of novel monoclonal antibodies was evaluated for antiviral efficacy. We directly compared all variants, showing that convalescence greater than 5 months post-symptom onset from ancestral virus provides little protection against SARS-CoV-2 variants. Vaccination enhances immunity against viral variants, except for Omicron BA.1, while a three-dose vaccine regimen provides over 50-fold enhanced protection against Omicron BA.1 compared to a two-dose. A novel Mab neutralizes Omicron BA.1 and BA.2 variants better than the clinically approved Mabs, although neither can neutralize Omicron BA.4 or BA.5. Thus, the need remains for continued vaccination-booster efforts, with innovation for vaccine and Mab improvement for broadly neutralizing activity. The usefulness of specific Mab applications links with the window of clinical opportunity when a cognate viral variant is present in the infected population.

Funder

National Institutes of Health

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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