Gupta Satish Kumar
Reproductive Cell Biology Laboratory, National Institute of Immunology, New Delhi, India.
HIV AIDS (Auckl). 2013 Oct 22;5:295-307. doi: 10.2147/HIV.S39164.
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.
杀菌剂主要用作局部暴露前预防药物,已被提议用于预防艾滋病毒的性传播。本综述涵盖了开发安全有效的杀菌剂以预防性传播艾滋病毒的趋势和挑战。杀菌剂开发的初始阶段使用了诸如壬苯醇醚-9(N-9)、C13G和月桂醇硫酸酯钠等表面活性剂,旨在使病毒失活。基于N-9和C31G的杀菌剂临床试验未能抑制艾滋病毒的性传播。相反,N-9增强了对HIV-1性传播的易感性。随后,对基于聚阴离子和多种其他抑制病毒与宿主细胞结合、融合或进入的化合物的杀菌剂在不同临床环境中的疗效进行了评估。这些试验中的大多数未能显示出预防艾滋病毒传播的安全性或有效性。杀菌剂开发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菌剂在一项IIb期试验(CAPRISA 004)中以性交依赖方式进行测试时发现,与安慰剂对照相比,使用替诺福韦凝胶的人感染艾滋病毒的可能性降低了39%。然而,在另一项试验(VOICE MTN 003)中,以性交独立模式每日使用一次的替诺福韦凝胶未能显示出预防艾滋病毒感染的任何疗效。替诺福韦凝胶目前正在南非进行一项III期安全性和疗效试验(FACTS 001),采用性交依赖给药方案。此外,用于缓慢释放诸如达匹韦林等抗逆转录病毒药物的长效杀菌剂递送系统(阴道环)也正在进行临床试验。发现新的作为保护效力相关指标的标志物、具有改善的杀菌剂使用依从性的新型长效递送系统、发现对广泛的艾滋病毒株有效的新化合物、开发包含针对其他性传播感染的额外疗效特征的多用途技术以及避孕将有助于推动杀菌剂开发领域向前发展。