Clinical use of vaginal or rectally applied microbicides in patients suffering from HIV/AIDS.

Satish Kumar Gupta, Nutan
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引用次数: 22

Abstract

Microbicides, primarily used as topical pre-exposure prophylaxis, have been proposed to prevent sexual transmission of HIV. This review covers the trends and challenges in the development of safe and effective microbicides to prevent sexual transmission of HIV Initial phases of microbicide development used such surfactants as nonoxynol-9 (N-9), C13G, and sodium lauryl sulfate, aiming to inactivate the virus. Clinical trials of microbicides based on N-9 and C31G failed to inhibit sexual transmission of HIV. On the contrary, N-9 enhanced susceptibility to sexual transmission of HIV-1. Subsequently, microbicides based on polyanions and a variety of other compounds that inhibit the binding, fusion, or entry of virus to the host cells were evaluated for their efficacy in different clinical setups. Most of these trials failed to show either safety or efficacy for prevention of HIV transmission. The next phase of microbicide development involved antiretroviral drugs. Microbicide in the form of 1% tenofovir vaginal gel when tested in a Phase IIb trial (CAPRISA 004) in a coitally dependent manner revealed that tenofovir gel users were 39% less likely to become HIV-infected compared to placebo control. However, in another trial (VOICE MTN 003), tenofovir gel used once daily in a coitally independent mode failed to show any efficacy to prevent HIV infection. Tenofovir gel is currently in a Phase III safety and efficacy trial in South Africa (FACTS 001) employing a coitally dependent dosing regimen. Further, long-acting microbicide-delivery systems (vaginal ring) for slow release of such antiretroviral drugs as dapivirine are also undergoing clinical trials. Discovering new markers as correlates of protective efficacy, novel long-acting delivery systems with improved adherence in the use of microbicides, discovering new compounds effective against a broad spectrum of HIV strains, developing multipurpose technologies incorporating additional features of efficacy against other sexually transmitted infections, and contraception will help in moving the field of microbicide development forward.

Abstract Image

艾滋病毒/艾滋病患者阴道或直肠应用杀菌剂的临床应用。
杀微生物剂,主要用作局部暴露前预防,已被提议防止艾滋病毒的性传播。本文综述了安全有效的杀菌剂的发展趋势和面临的挑战,以防止艾滋病毒的性传播。杀菌剂开发的最初阶段使用的表面活性剂如壬氧醇-9 (N-9)、C13G和十二烷基硫酸钠,旨在灭活病毒。基于N-9和C31G的杀微生物剂的临床试验未能抑制HIV的性传播。相反,N-9增加了HIV-1性传播的易感性。随后,以多阴离子为基础的杀菌剂和多种其他化合物抑制病毒的结合、融合或进入宿主细胞,在不同的临床设置中评估了它们的功效。这些试验大多未能显示出预防艾滋病毒传播的安全性或有效性。杀菌剂发展的下一阶段涉及抗逆转录病毒药物。1%替诺福韦阴道凝胶形式的杀微生物剂在IIb期试验(CAPRISA 004)中以性交依赖的方式进行测试时显示,与安慰剂对照组相比,替诺福韦凝胶使用者感染hiv的可能性降低39%。然而,在另一项试验(VOICE MTN 003)中,在不依赖性交的模式下每天使用一次替诺福韦凝胶未能显示出预防艾滋病毒感染的任何功效。替诺福韦凝胶目前正在南非进行一项III期安全性和有效性试验(FACTS 001),采用的是一种两性依赖的给药方案。此外,用于缓慢释放抗逆转录病毒药物如达匹维林的长效杀微生物剂输送系统(阴道环)也正在进行临床试验。发现与保护功效相关的新标记,在使用杀微生物剂时提高依从性的新型长效给药系统,发现对广泛的艾滋病毒毒株有效的新化合物,开发包含其他性传播感染功效特征的多用途技术,以及避孕将有助于推动杀微生物剂领域的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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