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• W2892314541 abstract "The therapeutic efficacy of oncolytic viral therapy often comes as a tradeoff with safety, such that potent vectors are often associated with toxicity, while safer viruses tend to have attenuated therapeutic effects. Despite promising preclinical data, the development of VSV as a clinical agent has been substantially hampered by the fact that severe neurotoxicity and hepatotoxicity have been observed in rodents and nonhuman primates in response to treatment with wild-type VSV. Although NDV has been shown to have an attractive safety profile in humans and to have promising oncolytic effects, its further development has been severely restricted due to the environmental risks that it poses. The hybrid rVSV-NDV vector, therefore, represents an extremely promising vector platform in that it has been rationally designed to be safe, with respect to both the recipient and the environment, while being simultaneously effective, both through its direct oncolytic actions and through induction of immunogenic cell death." @default.
• W2892314541 created "2018-09-27" @default.
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• W2892314541 date "2018-12-01" @default.
• W2892314541 modified "2023-10-12" @default.
• W2892314541 title "A Novel Chimeric Oncolytic Virus Vector for Improved Safety and Efficacy as a Platform for the Treatment of Hepatocellular Carcinoma" @default.
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• W2892314541 doi "https://doi.org/10.1128/jvi.01386-18" @default.
• W2892314541 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6232488" @default.
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