Crucitti Giuliana C, Botta Maurizio, Di Santo Roberto
Pasteur Institute, Fondazione Cenci Bolognetti, Dipartimento di Chimica e Tecnologie del Farmaco, Facoltà di Farmacia e Medicina, Sapienza Università di Roma, I-00185 Roma, Italy.
Curr HIV Res. 2012 Jan 1;10(1):36-41. doi: 10.2174/157016212799304706.
Microbicides are products that can be applied to vaginal or rectal mucosal surfaces with the goal of preventing, or at least significantly reducing, the transmission of sexually transmitted infections including HIV-1. Despite more than two decades of HIV-1 research, there is still no efficacious HIV-1 vaccine, and the scientific community appears sceptical about the short or long-term feasibility of developing a vaccine that has the ability to induce sterilizing immunity against HIV-1. In this setting, microbicide research has been developed. Among the promising candidate microbicides, the integrase inhibitors are the most recently developed compounds. In fact, since the beginning reverse transcriptase, fusion and entry inhibitors were identified as possible HIV-specific candidate microbicides along with the non-specific topical microbicides. In the case of integrase inhibitors, only a few have demonstrated to block HIV-1 infection in models that mimic sexual transmission of the virus. These compounds have been tested in in vitro and ex vivo assays to determine their efficacy in pre- and/or post-exposure prophylactic settings. In particular, the naphthyridinecarboxyamide L-870,812 has been shown to block viral infection in pre- and post-exposure studies obtaining comparable results to the reverse transcriptase inhibitor PMPA. The purpose of this article is to provide an overview of integrase inhibitors as potential topical microbicides and their comparative evaluation with HIV-specific and non-specific microbicides.
杀微生物剂是可应用于阴道或直肠粘膜表面的产品,目的是预防或至少显著减少包括HIV-1在内的性传播感染的传播。尽管对HIV-1进行了二十多年的研究,但仍然没有有效的HIV-1疫苗,科学界似乎对开发一种能够诱导对HIV-1产生绝育免疫力的疫苗的短期或长期可行性持怀疑态度。在这种情况下,杀微生物剂研究得到了发展。在有前景的候选杀微生物剂中,整合酶抑制剂是最近开发的化合物。事实上,自一开始,逆转录酶、融合和进入抑制剂就与非特异性局部杀微生物剂一起被确定为可能的HIV特异性候选杀微生物剂。就整合酶抑制剂而言,只有少数在模拟病毒性传播的模型中证明能阻断HIV-1感染。这些化合物已在体外和离体试验中进行测试,以确定它们在暴露前和/或暴露后预防环境中的功效。特别是,萘啶羧酰胺L-870,812在暴露前和暴露后研究中均显示能阻断病毒感染,获得了与逆转录酶抑制剂替诺福韦酯相当的结果。本文的目的是概述整合酶抑制剂作为潜在局部杀微生物剂的情况,以及它们与HIV特异性和非特异性杀微生物剂的比较评估。