A lipid nanoparticle mRNA vaccine expressing the Ebola virus glycoprotein elicits strong immunological response and provides protection against challenge
作者
Sandia National Laboratories (SNL-CA), Livermore, CA (United States),Elvia E. Silva,Defense Threat Reduction Agency,USDOE National Nuclear Security Administration (NNSA),Iris K. A. Jones,Zachary R. Stromberg,Steven B. Bradfute,Jason T. Ladner,Jay W. Hooper,Amy Rasley,Nicholas Fisher,Oscar A Negrete
Zaire Ebola virus (ZEBOV) is the causative agent behind ebola virus disease (EVD), a disease characterized by hemorrhagic fever and a high case fatality rate.Current countermeasures for EVD are limited to monoclonal antibody therapies, and a vesicular stomatitis virus (VSV)-vectored vaccine.Although the available therapies and vaccine have shown promise during recent ZEBOV outbreaks, long term protection and cross-protection against other viral species associated with EVD remain unknown.The rVSV-ZEBOV glycoprotein (gp) vaccine is currently considered the gold-standard and is recommended for pre-exposure prophylactic use in the US among high-risk populations, including military and health-care workers deployed in EVD response areas.Here, we developed a lipid nanoparticle (LNP) mRNA vaccine expressing the EBOVgp antigen and compared immunological responses from a prime-boost regimen of a lipid nanoparticle (LNP) mRNA vaccine formulation versus a rVSV-EBOVgp platform vaccine in wild type and immunocompromised mouse models.