Antigenic mapping and functional characterization of human New World hantavirus neutralizing antibodies

Author:

Engdahl Taylor B1ORCID,Binshtein Elad2,Brocato Rebecca L3,Kuzmina Natalia A45,Principe Lucia M3,Kwilas Steven A3ORCID,Kim Robert K3,Chapman Nathaniel S1,Porter Monique S1,Guardado-Calvo Pablo6ORCID,Rey Félix A6ORCID,Handal Laura S2,Diaz Summer M2,Zagol-Ikapitte Irene A7,Tran Minh H7,McDonald W Hayes7,Meiler Jens8ORCID,Reidy Joseph X2,Trivette Andrew2,Bukreyev Alexander459ORCID,Hooper Jay W3,Crowe James E1210ORCID

Affiliation:

1. Department of Pathology, Microbiology and Immunology, Vanderbilt University

2. Vanderbilt Vaccine Center, Vanderbilt University Medical Center

3. Virology Division, United States Army Medical Research Institute of Infectious Diseases

4. Department of Pathology, The University of Texas Medical Branch at Galveston

5. Galveston National Laboratory

6. Institut Pasteur, Université Paris Cité

7. Department of Biochemistry and Mass Spectrometry Research Center, Vanderbilt University

8. Department of Chemistry, Vanderbilt University

9. Department of Microbiology and Immunology, University of Texas Medical Branch

10. Department of Pediatrics, Vanderbilt University Medical Center

Abstract

Hantaviruses are high-priority emerging pathogens carried by rodents and transmitted to humans by aerosolized excreta or, in rare cases, person-to-person contact. While infections in humans are relatively rare, mortality rates range from 1 to 40% depending on the hantavirus species. There are currently no FDA-approved vaccines or therapeutics for hantaviruses, and the only treatment for infection is supportive care for respiratory or kidney failure. Additionally, the human humoral immune response to hantavirus infection is incompletely understood, especially the location of major antigenic sites on the viral glycoproteins and conserved neutralizing epitopes. Here, we report antigenic mapping and functional characterization for four neutralizing hantavirus antibodies. The broadly neutralizing antibody SNV-53 targets an interface between Gn/Gc, neutralizes through fusion inhibition and cross-protects against the Old World hantavirus species Hantaan virus when administered pre- or post-exposure. Another broad antibody, SNV-24, also neutralizes through fusion inhibition but targets domain I of Gc and demonstrates weak neutralizing activity to authentic hantaviruses. ANDV-specific, neutralizing antibodies (ANDV-5 and ANDV-34) neutralize through attachment blocking and protect against hantavirus cardiopulmonary syndrome (HCPS) in animals but target two different antigenic faces on the head domain of Gn. Determining the antigenic sites for neutralizing antibodies will contribute to further therapeutic development for hantavirus-related diseases and inform the design of new broadly protective hantavirus vaccines.

Funder

National Institute of Allergy and Infectious Diseases

Military Infectious Diseases Program

NIH Office of the Director

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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