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A Topical Microbicide Gel Formulation of CCR5 Antagonist Maraviroc Prevents HIV-1 Vaginal Transmission in Humanized RAG-hu Mice

机译:CCR5拮抗剂Maraviroc的局部杀菌凝胶制剂可预防人源化RAG-hu小鼠中的HIV-1阴道传播。

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摘要

For prevention of HIV infection many currently licensed anti-HIV drugs and new ones in the pipeline show potential as topically applied microbicides. While macaque models have been the gold standard for in vivo microbicide testing, they are expensive and sufficient numbers are not available. Therefore, a small animal model that facilitates rapid evaluation of potential candidates for their preliminary efficacy is urgently needed in the microbicide field. We previously demonstrated that RAG-hu humanized mouse model permits HIV-1 mucosal transmission via both vaginal and rectal routes and that oral pre-exposure chemo-prophylactic strategies could be tested in this system. Here in these proof-of-concept studies, we extended this system for topical microbicide testing using HIV-1 as the challenge virus. Maraviroc, a clinically approved CCR5 inhibitor drug for HIV treatment, was formulated as a microbicide gel at 5 mM concentration in 2.2% hydroxyl ethyl cellulose. Female RAG-hu mice were challenged vaginally with HIV-1 an hour after intravaginal application of the maraviroc gel. Our results showed that maraviroc gel treated mice were fully protected against vaginal HIV-1 challenge in contrast to placebo gel treated mice which all became infected. These findings highlight the utility of the humanized mouse models for microbicide testing and, together with the recent data from macaque studies, suggest that maraviroc is a promising candidate for future microbicide clinical trials in the field.
机译:为了预防HIV感染,许多当前许可的抗HIV药物和正在开发中的新药显示出作为局部应用杀微生物剂的潜力。尽管猕猴模型已成为体内杀微生物剂测试的金标准,但它们昂贵且无法提供足够的数量。因此,在杀微生物剂领域迫切需要一种小型动物模型,该模型有助于快速评估潜在候选物的初步功效。我们以前证明了RAG-hu人源化小鼠模型允许HIV-1通过阴道和直肠途径进行粘膜传播,并且可以在该系统中测试口服暴露前的化学预防策略。在这些概念验证研究中,我们将该系统扩展为使用HIV-1作为攻击病毒进行局部杀微生物剂测试。 Maraviroc是临床批准的用于HIV治疗的CCR5抑制剂药物,被配制为在2.2%羟乙基纤维素中浓度为5 mM的杀菌剂凝胶。在阴道内施用maraviroc凝胶一小时后,对雌性RAG-hu小鼠进行阴道HIV-1攻击。我们的结果表明,与所有被感染的安慰剂凝胶治疗的小鼠相比,马拉维罗凝胶治疗的小鼠可充分防御阴道HIV-1攻击。这些发现凸显了人源化小鼠模型在杀微生物剂测试中的实用性,以及猕猴研究的最新数据,表明maraviroc是该领域未来杀微生物剂临床试验的有希望的候选者。

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