Antibodies Elicited by an NS1-Based Vaccine Protect Mice against Zika Virus

Author:

Bailey Mark J.12,Broecker Felix1,Duehr James12,Arumemi Fortuna3,Krammer Florian1ORCID,Palese Peter14,Tan Gene S.35

Affiliation:

1. Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA

2. Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA

3. Infectious Diseases, The J. Craig Venter Institute, La Jolla, California, USA

4. Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA

5. Department of Medicine, University of California San Diego, La Jolla, California, USA

Abstract

Zika virus is a global public health threat that causes microcephaly and congenital malformations in newborns and Guillain-Barré syndrome in adults. Currently, no vaccines or treatments are available. While antibodies targeting the envelope glycoprotein can neutralize virus, they carry the risk of antibody-dependent enhancement of disease (ADE). In contrast, antibodies generated against the NS1 protein can be protective without eliciting ADE. The present study demonstrates the effectiveness of an NS1-based vaccine in eliciting high titers of protective antibodies against Zika virus disease in a mouse model. Sera generated by this vaccine can elicit Fc-mediated effector functions against Zika virus-infected cells. Lastly, we provide human data suggesting that the antibody response against the Zika virus NS1 protein is long-lasting and functionally active. Overall, our work will inform the development of a safe and effective Zika virus vaccine.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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