Broadly neutralizing monoclonal antibodies protect against multiple tick-borne flaviviruses

Author:

VanBlargan Laura A.1ORCID,Errico John M.2ORCID,Kafai Natasha M.12ORCID,Burgomaster Katherine E.3ORCID,Jethva Prashant N.4ORCID,Broeckel Rebecca M.5ORCID,Meade-White Kimberly5ORCID,Nelson Christopher A.2ORCID,Himansu Sunny6ORCID,Wang David7ORCID,Handley Scott A.2ORCID,Gross Michael L.4ORCID,Best Sonja M.5ORCID,Pierson Theodore C.3ORCID,Fremont Daved H.2789ORCID,Diamond Michael S.1279ORCID

Affiliation:

1. Department of Medicine, Washington University School of Medicine, St. Louis, MO

2. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO

3. Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD

4. Department of Chemistry, Washington University, St. Louis, MO

5. Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT

6. Moderna, Inc., Cambridge, MA

7. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO

8. Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO

9. Andrew M. and Jane M. Bursky Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO

Abstract

Although Powassan virus (POWV) is an emerging tick-transmitted flavivirus that causes severe or fatal neuroinvasive disease in humans, medical countermeasures have not yet been developed. Here, we developed a panel of neutralizing anti-POWV mAbs recognizing six distinct antigenic sites. The most potent of these mAbs bind sites within domain II or III of the envelope (E) protein and inhibit postattachment viral entry steps. A subset of these mAbs cross-react with other flaviviruses. Both POWV type–specific and cross-reactive neutralizing mAbs confer protection in mice against POWV infection when given as prophylaxis or postexposure therapy. Several cross-reactive mAbs mapping to either domain II or III also protect in vivo against heterologous tick-transmitted flaviviruses including Langat and tick-borne encephalitis virus. Our experiments define structural and functional correlates of antibody protection against POWV infection and identify epitopes targeted by broadly neutralizing antibodies with therapeutic potential against multiple tick-borne flaviviruses.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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