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A Cloned Recombinant Vesicular Stomatitis Virus-Vectored Marburg Vaccine, PHV01, Protects Guinea Pigs from Lethal Marburg Virus Disease. | LitMetric

AI Article Synopsis

  • - Marburg virus (MARV) causes severe hemorrhagic fever with high mortality rates, and currently, there are no approved treatments or vaccines for it.
  • - Researchers tested a recombinant vesicular stomatitis virus (rVSV)-based vaccine, PHV01, which incorporates MARV's glycoprotein, and found that it provided full protection in guinea pigs against lethal MARV doses.
  • - The study suggests the guinea pig model is useful for evaluating MARV vaccines, and it highlights PHV01 as a promising candidate for further development.

Article Abstract

Marburg virus (MARV) is a negative-sense, single-stranded RNA virus that belongs to the family. Despite having caused numerous outbreaks of severe hemorrhagic fever with high case fatality rates, there are still no clinically approved therapeutics or vaccines to treat or prevent MARV disease. Recombinant vesicular stomatitis viruses (rVSVs) expressing heterologous viral glycoproteins have shown remarkable promise as live-attenuated vaccine vectors, with an rVSV-based Ebola virus vaccine having received regulatory approval in the United States and numerous other countries. Analogous rVSV vaccine vectors have also been developed for MARV and have shown efficacy in several preclinical studies conducted in nonhuman primates. Here, we used a guinea pig model to confirm the protective efficacy of a cloned, rVSV-based candidate vaccine, termed PHV01, expressing the MARV variant Angola glycoprotein. Our results demonstrated that a single dose (2 × 10 PFU) of vaccine administered 28 days prior to challenge with a uniformly lethal dose of guinea-pig-adapted MARV variant Angola provided complete protection from death and disease. Moreover, protection was robust, with as little as 200 PFU of vaccine conferring significant protection. Not only does this study highlight the potential predictive value of the guinea pig model in the evaluation of MARV countermeasures, but it also demonstrates consistent and reproducible protection afforded by a clonal vaccine candidate. Indeed, this study identifies PHV01 as a suitable vaccine candidate for advanced development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324024PMC
http://dx.doi.org/10.3390/vaccines10071004DOI Listing

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