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


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 10 09 2021
accepted: 12 10 2021
entrez: 15 11 2021
pubmed: 16 11 2021
medline: 11 2 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34777392
doi: 10.3389/fimmu.2021.774026
pmc: PMC8578864
doi:

Substances chimiques

Antibodies, Viral 0
Antigens, Viral 0
Biomarkers 0
Cytokines 0
Immunoglobulin G 0
Immunoglobulin M 0
Viral Vaccines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

774026

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001414
Pays : United States

Informations de copyright

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

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Andrea Marzi (A)

Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.

Allen Jankeel (A)

Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.

Andrea R Menicucci (AR)

Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.

Julie Callison (J)

Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.

Kyle L O'Donnell (KL)

Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.

Friederike Feldmann (F)

Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.

Amanda N Pinski (AN)

Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.

Patrick W Hanley (PW)

Rocky Mountain Veterinary Branch, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States.

Ilhem Messaoudi (I)

Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.

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Classifications MeSH