Evaluation of a Single-Dose Nucleoside-Modified Messenger RNA Vaccine Encoding Hendra Virus-Soluble Glycoprotein Against Lethal Nipah virus Challenge in Syrian Hamsters

Author:

Lo Michael K1ORCID,Spengler Jessica R1,Welch Stephen R1,Harmon Jessica R1,Coleman-McCray JoAnn D1,Scholte Florine E M1,Shrivastava-Ranjan Punya1,Montgomery Joel M1,Nichol Stuart T1,Weissman Drew2,Spiropoulou Christina F1

Affiliation:

1. Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

2. Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA

Abstract

Abstract In the absence of approved vaccines and therapeutics for use in humans, Nipah virus (NiV) continues to cause fatal outbreaks of encephalitis and respiratory disease in Bangladesh and India on a near-annual basis. We determined that a single dose of a lipid nanoparticle nucleoside-modified messenger RNA vaccine encoding the soluble Hendra virus glycoprotein protected up to 70% of Syrian hamsters from lethal NiV challenge, despite animals having suboptimally primed immune responses before challenge. These data provide a foundation from which to optimize future messenger RNA vaccination studies against NiV and other highly pathogenic viruses.

Funder

Oak Ridge Institute for Science and Education

U.S. Department of Energy

CDC Emerging Infectious Disease Research Core funds

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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