Hendrix Craig W, Cao Ying Jun, Fuchs Edward J
Division of Clinical Pharmacology, Johns Hopkins University School of Medicine, USA.
Annu Rev Pharmacol Toxicol. 2009;49:349-75. doi: 10.1146/annurev.pharmtox.48.113006.094906.
Microbicides, substances applied topically to prevent sexual HIV infection, are needed to empower receptive sexual partners with effective prevention methods. Several large microbicide trials, however, failed to demonstrate efficacy, thus motivating a reevaluation of the current microbicide development paradigm, which has been largely empirically based. Microbicide use occurs in a highly complex environment involving multi-level interactions, behavioral and biochemical, among host, virus, and drug, yet many details of these interactions remain unknown. Fundamental information regarding virus and drug distribution over time in sexually receptive body compartments that is necessary to design a microbicide able to outdistance and outlast the virus is largely absent. Recent efforts have been made to establish a simple conceptual framework for obtaining the knowledge that is likely to inform a more mechanistic, model-based development paradigm. These efforts have also advanced the development of numerous methodological approaches to obtain the knowledge needed to improve microbicide development.
杀微生物剂是局部应用以预防性传播艾滋病毒感染的物质,需要通过有效的预防方法使性伴侣中的接受方获得保护。然而,几项大型杀微生物剂试验未能证明其有效性,因此促使人们重新评估当前主要基于经验的杀微生物剂开发模式。杀微生物剂的使用发生在一个高度复杂的环境中,涉及宿主、病毒和药物之间多层次的行为和生化相互作用,但这些相互作用的许多细节仍不清楚。对于设计一种能够超越并持久抵御病毒的杀微生物剂而言,至关重要的关于病毒和药物在性接受性身体腔室中随时间分布的基础信息基本缺失。最近已做出努力,建立一个简单的概念框架,以获取可能为更具机制性、基于模型的开发模式提供信息的知识。这些努力还推动了众多方法学途径的发展,以获取改善杀微生物剂开发所需的知识。