抗病毒治疗的未来展望。

E H Wiltink
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引用次数: 0

摘要

开发有效无毒抗病毒药物的两个重要障碍是病毒的细胞内定位和病毒利用宿主细胞功能繁殖的事实。因此,新的抗病毒药物必须作用于病毒特异性功能。目前大多数可用的抗病毒药物都是对大量可能的药物进行复合筛选的结果。我们对病毒增殖周期的分子生物学和生物化学的理解的进步,以及用于确定作用分子位点的新实验室技术,现在使得以更有目的的方式开发和筛选新的抗病毒药物成为可能。抗病毒治疗的另一种可能的选择是使用增强治疗效果或减少副作用的药物进行联合治疗。根据它们在病毒增殖过程中作用的不同步骤,讨论了最有前途的新型抗病毒药物。并对联合治疗进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future prospects in antiviral therapy.

Two important stumbling blocks to the development of effective and nontoxic antiviral drugs are the intracellular localization of the virus and the fact that a virus uses host cell functions to multiply. Therefore, new antiviral drugs must act on a virus-specific function. Most currently available useful antiviral drugs are the result of compound screening of large numbers of possible agents. Advances in our understanding of the molecular biology and biochemistry of the viral multiplication cycle and new laboratory techniques for determining the molecular sites of action have now made it possible to develop and screen new antiviral drugs in a more purposeful manner. Another possible option in antiviral therapy is combination therapy using drugs that enhance the therapeutic effect or diminish side-effects. The most promising new antiviral drugs are discussed according to the different steps they affect in the viral multiplication process. Combination therapy is also reviewed.

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