| Literature DB >> 33352786 |
Joan G Tell1, Beth-Ann G Coller1, Sheri A Dubey1, Ursula Jenal2, William Lapps1, Liman Wang1, Jayanthi Wolf1.
Abstract
rVSVΔG-ZEBOV-GP is a live, attenuated, recombinant vesicular stomatitis virus (rVSV)-based vaccine for the prevention of Ebola virus disease caused by Zaire ebolavirus. As a replication-competent genetically modified organism, rVSVΔG-ZEBOV-GP underwent various environmental evaluations prior to approval, the most in-depth being the environmental risk assessment (ERA) required by the European Medicines Agency. This ERA, as well as the underlying methodology used to arrive at a sound conclusion about the environmental risks of rVSVΔG-ZEBOV-GP, are described in this review. Clinical data from vaccinated adults demonstrated only infrequent, low-level shedding and transient, low-level viremia, indicating a low person-to-person infection risk. Animal data suggest that it is highly unlikely that vaccinated individuals would infect animals with recombinant virus vaccine or that rVSVΔG-ZEBOV-GP would spread within animal populations. Preclinical studies in various hematophagous insect vectors showed that these species were unable to transmit rVSVΔG-ZEBOV-GP. Pathogenicity risk in humans and animals was found to be low, based on clinical and preclinical data. The overall risk for non-vaccinated individuals and the environment is thus negligible and can be minimized further through defined mitigation strategies. This ERA and the experience gained are relevant to developing other rVSV-based vaccines, including candidates under investigation for prevention of COVID-19.Entities:
Keywords: ERA; ERVEBO®; GMO; Zaire ebolavirus; environmental impact; rVSV; recombinant vaccine; shedding; vesicular stomatitis virus; viremia
Year: 2020 PMID: 33352786 PMCID: PMC7767225 DOI: 10.3390/vaccines8040779
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X