Single Dose of a VSV-Based Vaccine Rapidly Protects Macaques From Marburg Virus Disease.
Animals
Antibodies, Viral
/ immunology
Antigens, Viral
/ immunology
B-Lymphocytes
/ immunology
Biomarkers
Chlorocebus aethiops
Cytokines
/ blood
Disease Models, Animal
Immunization
Immunoglobulin G
/ immunology
Immunoglobulin M
/ immunology
Lymphocyte Activation
Marburg Virus Disease
/ blood
Marburgvirus
/ immunology
Vaccination
Vero Cells
Vesiculovirus
Viral Load
Viral Vaccines
/ administration & dosage
Filovirus
MARV Angola
MVD
time to immunity
transcriptomics
vesicular stomatitis virus
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
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
774026Subventions
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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