Olasunkanmi Oluwatayo Israel, Zhong Zhao-Hua
Department of Microbiology, Harbin Medical University, Harbin, 150081, China.
J Virus Erad. 2022 Jun 20;8(2):100074. doi: 10.1016/j.jve.2022.100074. eCollection 2022 Jun.
Coxsackievirus B3 (CVB3) infections may cause life-threatening diseases and have no approved specific treatment. Some promising approaches to treat viral diseases include drug repurposing and combination therapy. We have selected in this study dasabuvir, an approved antiviral drug, and PSI-6206, an experimental drug and determined their individual and combined antiviral activity against CVB3 replication . Our results show that the individual drugs inhibited CVB3 infection in a dose-dependent manner, at a selective index >10 with a strong synergetic antiviral effect of the two compounds. Given that dasabuvir has already been approved for the treatment of hepatitis C virus infection, treatment of CVB3-related disease with this drug may represent a promising treatment strategy.
柯萨奇病毒B3(CVB3)感染可能导致危及生命的疾病,且尚无获批的特异性治疗方法。一些治疗病毒性疾病的有前景的方法包括药物再利用和联合疗法。在本研究中,我们选择了已获批的抗病毒药物达沙布韦和一种实验性药物PSI-6206,并确定了它们针对CVB3复制的单独及联合抗病毒活性。我们的结果表明,这两种药物均以剂量依赖性方式抑制CVB3感染,选择性指数>10,且两种化合物具有很强的协同抗病毒作用。鉴于达沙布韦已获批用于治疗丙型肝炎病毒感染,用该药物治疗CVB3相关疾病可能是一种有前景的治疗策略。