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Rapid protection of nonhuman primates against Marburg virus disease using a single low-dose VSV-based vaccine.
- Source :
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EBioMedicine [EBioMedicine] 2023 Mar; Vol. 89, pp. 104463. Date of Electronic Publication: 2023 Feb 10. - Publication Year :
- 2023
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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