| Literature DB >> 30499341 |
Yang Wang1, Xiaobing Zhou2, Zhen Wu1, Han Hu1, Jing Jin1, Yanping Hu2, Yuting Dong3, Jianwen Zou3, Zeyong Mao3, Xiaotai Shi3, Yan Huo2, Jianjun Lyu2, Zhizheng Fang3, Wen Zhang4, Yujie Zhu4, Bo Li2, Binlei Liu1,3.
Abstract
Oncolytic virotherapy is a new and safe therapeutic strategy based on the inherent cytotoxicity of oncolytic viruses and their ability to replicate and spread within tumors in a selective manner. In a previous study, a new type of oncolytic herpes simplex virus type 2 (oHSV-2, named OH2) was constructed to treat human cancers. That study demonstrated that OH2 is genetically and biologically stable. Its antitumor activity was maintained, even after passaging the virus for >20 generations. To advance OH2 into a clinical trial, a systematic preclinical safety evaluation was performed, which included: an acute toxicity test of OH2 in BALB/c mice; repeated dose toxicity tests of OH2 in BALB/c mice and cynomolgus monkeys; and biodistribution assays of OH2 in BALB/c mice, tumor-bearing mice, tumor-bearing nude mice, and cynomolgus monkeys. The results of this preclinical safety evaluation of OH2 indicate that OH2 is safe and suitable for clinical trials.Entities:
Keywords: antitumor effect; herpes simplex virus type 2; safety evaluation
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Year: 2019 PMID: 30499341 DOI: 10.1089/hum.2018.170
Source DB: PubMed Journal: Hum Gene Ther ISSN: 1043-0342 Impact factor: 5.695