Tam R C, Lau J Y, Hong Z
Research and Development, ICN Pharmaceuticals, Costa Mesa, Calif, USA.
Antivir Chem Chemother. 2001 Sep;12(5):261-72. doi: 10.1177/095632020101200501.
Although ribavirin was originally synthesized over 30 years ago and has been used to treat viral infections as monotherapy (respiratory syncytial virus and Lassa fever virus) or with interferon-alpha (IFN-alpha) as combination therapy (hepatitis C virus), the precise mechanism of its therapeutic activities remains controversial. In this review we focus on two main biological properties of ribavirin: its indirect and direct antiviral activities (with particular emphasis on its efficacy against chronic hepatitis C infection). Each property could individually or collectively account for its clinical efficacy against viral infections. First, with emphasis on the evidence for indirect activities of ribavirin, we will review the clinical observations that suggest that the immunomodulatory properties of ribavirin can in part account for its antiviral activities in vivo. We will then describe the mode of ribavirin's direct antiviral activities. These direct activities can be ascribed to several possible mechanisms, including the recently described activity as an RNA mutagen, a property that may be important in driving a rapidly mutating RNA virus over the threshold to 'error catastrophe'.
尽管利巴韦林在30多年前就已首次合成,并已被用于单药治疗病毒感染(呼吸道合胞病毒和拉沙热病毒)或与α干扰素(IFN-α)联合治疗(丙型肝炎病毒),但其治疗活性的确切机制仍存在争议。在本综述中,我们聚焦于利巴韦林的两个主要生物学特性:其间接和直接抗病毒活性(特别强调其对慢性丙型肝炎感染的疗效)。每种特性都可能单独或共同解释其对病毒感染的临床疗效。首先,着重于利巴韦林间接活性的证据,我们将回顾临床观察结果,这些结果表明利巴韦林的免疫调节特性在一定程度上可以解释其在体内的抗病毒活性。然后我们将描述利巴韦林直接抗病毒活性的模式。这些直接活性可归因于几种可能的机制,包括最近描述的作为RNA诱变剂的活性,这一特性在促使快速突变的RNA病毒超过阈值达到“错误灾难”方面可能很重要。