Broad and potent neutralizing human antibodies to tick-borne flaviviruses protect mice from disease

Author:

Agudelo Marianna1ORCID,Palus Martin23ORCID,Keeffe Jennifer R.4ORCID,Bianchini Filippo15ORCID,Svoboda Pavel36ORCID,Salát Jiří23ORCID,Peace Avery7ORCID,Gazumyan Anna1ORCID,Cipolla Melissa1ORCID,Kapoor Tania1ORCID,Guidetti Francesca1ORCID,Yao Kai-Hui1ORCID,Elsterová Jana23ORCID,Teislerová Dana8ORCID,Chrdle Aleš8910ORCID,Hönig Václav23ORCID,Oliveira Thiago1ORCID,West Anthony P.4ORCID,Lee Yu E.4ORCID,Rice Charles M.7ORCID,MacDonald Margaret R.7ORCID,Bjorkman Pamela J.4ORCID,Růžek Daniel23ORCID,Robbiani Davide F.15ORCID,Nussenzweig Michel C.111ORCID

Affiliation:

1. Laboratory of Molecular Immunology, The Rockefeller University, New York, NY

2. Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic

3. Veterinary Research Institute, Brno, Czech Republic

4. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA

5. Institute for Research in Biomedicine, Università della Svizzera italiana, Bellinzona, Switzerland

6. Department of Pharmacology and Pharmacy, Faculty of Veterinary Medicine, University of Veterinary and Pharmaceutical Sciences Brno, Brno, Czech Republic

7. Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY

8. Hospital České Budějovice, České Budějovice, Czech Republic

9. Faculty of Social and Health Sciences, University of South Bohemia, České Budějovice, Czech Republic

10. Royal Liverpool University Hospital, Liverpool, UK

11. Howard Hughes Medical Institute, The Rockefeller University, New York, NY

Abstract

Tick-borne encephalitis virus (TBEV) is an emerging human pathogen that causes potentially fatal disease with no specific treatment. Mouse monoclonal antibodies are protective against TBEV, but little is known about the human antibody response to infection. Here, we report on the human neutralizing antibody response to TBEV in a cohort of infected and vaccinated individuals. Expanded clones of memory B cells expressed closely related anti-envelope domain III (EDIII) antibodies in both groups of volunteers. However, the most potent neutralizing antibodies, with IC50s below 1 ng/ml, were found only in individuals who recovered from natural infection. These antibodies also neutralized other tick-borne flaviviruses, including Langat, louping ill, Omsk hemorrhagic fever, Kyasanur forest disease, and Powassan viruses. Structural analysis revealed a conserved epitope near the lateral ridge of EDIII adjoining the EDI–EDIII hinge region. Prophylactic or early therapeutic antibody administration was effective at low doses in mice that were lethally infected with TBEV.

Funder

National Institutes of Health

Czech Science Foundation

Czech Academy of Sciences

Ministry of Health of the Czech Republic

U.S. Department of Energy

Howard Hughes Medical Institute

Swiss National Science Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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