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Rapid protection of nonhuman primates against Marburg virus disease using a single low-dose VSV-based vaccine.

Authors :
O'Donnell KL
Feldmann F
Kaza B
Clancy CS
Hanley PW
Fletcher P
Marzi A
Source :
EBioMedicine [EBioMedicine] 2023 Mar; Vol. 89, pp. 104463. Date of Electronic Publication: 2023 Feb 10.
Publication Year :
2023

Abstract

Background: Marburg virus (MARV) is the causative agent of Marburg virus disease (MVD) which has a case fatality rate up to ∼90% in humans. Recently, there were cases reported in Guinea and Ghana highlighting this virus as a high-consequence pathogen potentially threatening global public health. There are no licensed treatments or vaccines available today. We used a vesicular stomatitis virus (VSV)-based vaccine expressing the MARV-Angola glycoprotein (VSV-MARV) as the viral antigen. Previously, a single dose of 1 × 10 <superscript>7</superscript> plaque-forming units (PFU) administered 7 days before challenge resulted in uniform protection from disease in cynomolgus macaques.<br />Methods: As we sought to lower the vaccination dose to achieve a higher number of vaccine doses per vial, we administered 1 × 10 <superscript>5</superscript> or 1 × 10 <superscript>3</superscript>  PFU 14 days or 1 × 10 <superscript>3</superscript>  PFU 7 days before challenge to cohorts of cynomolgus macaques and investigated immunity as well as protective efficacy.<br />Results: Vaccination resulted in uniform protection with no detectable viremia. Antigen-specific IgG responses were induced by both vaccine concentrations and were sustained until the study endpoint. Neutralizing antibody responses and antibody-dependent cellular phagocytosis were observed. The cellular response after vaccination was characterized by an early induction of NK cell activation. Additionally, antigen-specific memory T cell subsets were detected in all vaccination cohorts indicating that while the primary protective mechanism of VSV-MARV is the humoral response, a functional cellular response is also induced.<br />Interpretation: Overall, this data highlights VSV-MARV as a viable and fast-acting MARV vaccine candidate suitable for deployment in emergency outbreak situations and supports its clinical development.<br />Funding: This work was funded by the Intramural Research Program NIAID, NIH.<br />Competing Interests: Declaration of interests The authors declare no conflict of interest.<br /> (Published by Elsevier B.V.)

Details

Language :
English
ISSN :
2352-3964
Volume :
89
Database :
MEDLINE
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
36774693
Full Text :
https://doi.org/10.1016/j.ebiom.2023.104463