Single Dose of a VSV-Based Vaccine Rapidly Protects Macaques From Marburg Virus Disease

  • Andrea Marzi
  • , Allen Jankeel
  • , Andrea R. Menicucci
  • , Julie Callison
  • , Kyle L. O’Donnell
  • , Friederike Feldmann
  • , Amanda N. Pinski
  • , Patrick W. Hanley
  • , Ilhem Messaoudi

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Marburg virus (MARV) is a member of the filovirus family that causes hemorrhagic disease with high case fatality rates. MARV is on the priority list of the World Health Organization for countermeasure development highlighting its potential impact on global public health. We developed a vesicular stomatitis virus (VSV)-based vaccine expressing the MARV glycoprotein (VSV-MARV) and previously demonstrated uniform protection of nonhuman primates (NHPs) with a single dose. Here, we investigated the fast-acting potential of this vaccine by challenging NHPs with MARV 14, 7 or 3 days after a single dose vaccination with VSV-MARV. We found that 100% of the animals survived when vaccinated 7 or 14 days and 75% of the animal survived when vaccinated 3 days prior to lethal MARV challenge. Transcriptional analysis of whole blood samples indicated activation of B cells and antiviral defense after VSV-MARV vaccination. In the day -14 and -7 groups, limited transcriptional changes after challenge were observed with the exception of day 9 post-challenge in the day -7 group where we detected gene expression profiles indicative of a recall response. In the day -3 group, transcriptional analysis of samples from surviving NHPs revealed strong innate immune activation. In contrast, the animal that succumbed to disease in this group lacked signatures of antiviral immunity. In summary, our data demonstrate that the VSV-MARV is a fast-acting vaccine suitable for the use in emergency situations like disease outbreaks in Africa.

Original languageEnglish
Article number774026
JournalFrontiers in Immunology
Volume12
DOIs
StatePublished - Oct 27 2021

Bibliographical note

Publisher Copyright:
© Copyright © 2021 Marzi, Jankeel, Menicucci, Callison, O’Donnell, Feldmann, Pinski, Hanley and Messaoudi.

Funding

We thank the staff of the Rocky Mountain Veterinary Branch (NIAID) for their support of the animal study. This work was supported by the Intramural Research Program NIAID, NIH and in part by the National Center for Research

FundersFunder number
Rocky Mountain Veterinary Branch
National Institutes of Health (NIH)
National Institute of Allergy and Infectious Diseases
National Center for Advancing Translational Sciences (NCATS)UL1TR001414

    Keywords

    • Filovirus
    • MARV Angola
    • MVD
    • time to immunity
    • transcriptomics
    • vesicular stomatitis virus

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology

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