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Combined antiviral activity of interferon-α and RNA interference directed against hepatitis C without affecting vector delivery and gene silencing

机译:干扰素-α和RNA干扰物对丙型肝炎的联合抗病毒活性而不会影响载体的递送和基因沉默

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摘要

The current standard interferon-alpha (IFN-α)-based therapy for chronic hepatitis C virus (HCV) infection is only effective in approximately half of the patients, prompting the need for alternative treatments. RNA interference (RNAi) represents novel approach to combat HCV by sequence-specific targeting of viral or host factors involved in infection. Monotherapy of RNAi, however, may lead to therapeutic resistance by mutational escape of the virus. Here, we proposed that combining lentiviral vector-mediated RNAi and IFN-α could be more effective and avoid therapeutic resistance. In this study, we found that IFN-α treatment did not interfere with RNAi-mediated gene silencing. RNAi and IFN-α act independently on HCV replication showing combined antiviral activity when used simultaneously or sequentially. Transduction of mouse hepatocytes in vivo and in vitro was not effected by IFN-α treatment. In conclusion, RNAi and IFN-α can be effectively combined without cross-interference and may represent a promising combinational strategy for the treatment of hepatitis C.
机译:当前用于慢性丙型肝炎病毒(HCV)感染的基于标准干扰素-α(IFN-α)的疗法仅在大约一半的患者中有效,这提示需要其他治疗方法。 RNA干扰(RNAi)代表了一种新方法,可通过对感染涉及的病毒或宿主因子进行序列特异性靶向来对抗HCV。但是,RNAi的单药治疗可能会由于病毒的突变逸出而导致治疗耐药性。在这里,我们建议将慢病毒载体介导的RNAi和IFN-α结合使用可能更有效,并且避免了治疗耐药性。在这项研究中,我们发现IFN-α处理不会干扰RNAi介导的基因沉默。 RNAi和IFN-α独立作用于HCV复制,当同时或顺序使用时显示出联合的抗病毒活性。体内和体外小鼠肝细胞的转导不受IFN-α处理的影响。总之,RNAi和IFN-α可以有效地结合而不会产生交叉干扰,并且可能代表了有希望的丙型肝炎联合治疗策略。

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