Koizumi Yoshiki, Iwami Shingo
Department of Biology, Faculty of Sciences, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
Theor Biol Med Model. 2014 Sep 25;11:41. doi: 10.1186/1742-4682-11-41.
In the current era of antiviral drug therapy, combining multiple drugs is a primary approach for improving antiviral effects, reducing the doses of individual drugs, relieving the side effects of strong antiviral drugs, and preventing the emergence of drug-resistant viruses. Although a variety of new drugs have been developed for HIV, HCV and influenza virus, the optimal combinations of multiple drugs are incompletely understood. To optimize the benefits of multi-drugs combinations, we must investigate the interactions between the combined drugs and their target viruses. Mathematical models of viral infection dynamics provide an ideal tool for this purpose. Additionally, whether drug combinations computed by these models are synergistic can be assessed by two prominent drug combination theories, Loewe additivity and Bliss independence. By combining the mathematical modeling of virus dynamics with drug combination theories, we could show the principles by which drug combinations yield a synergistic effect. Here, we describe the theoretical aspects of multi-drugs therapy and discuss their application to antiviral research.
在当前抗病毒药物治疗时代,联合使用多种药物是提高抗病毒效果、降低单一药物剂量、减轻强效抗病毒药物副作用以及预防耐药病毒出现的主要方法。尽管已经针对艾滋病毒、丙型肝炎病毒和流感病毒开发了多种新药,但多种药物的最佳组合尚未完全明确。为了优化多药联合的益处,我们必须研究联合药物与其靶病毒之间的相互作用。病毒感染动力学的数学模型为此提供了理想工具。此外,通过两种著名的药物联合理论——洛伊相加性和布利斯独立性,可以评估这些模型计算出的药物组合是否具有协同作用。通过将病毒动力学的数学建模与药物联合理论相结合,我们可以展示药物组合产生协同效应的原理。在此,我们描述多药治疗的理论方面,并讨论它们在抗病毒研究中的应用。