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5P12-RANTES(一种直肠微生态制剂候选物)在人体直肠灌洗液中的稳定性

Stability of 5P12-RANTES, A Candidate Rectal Microbicide, in Human Rectal Lavage.

作者信息

Cerini Fabrice, Offord Robin, McGowan Ian, Hartley Oliver

机构信息

1 Department of Pathology and Immunology, Faculty of Medicine, University of Geneva , Geneva, Switzerland .

2 The Mintaka Foundation for Medical Research , Geneva, Switzerland .

出版信息

AIDS Res Hum Retroviruses. 2017 Aug;33(8):768-777. doi: 10.1089/AID.2016.0199. Epub 2017 Mar 6.

DOI:10.1089/AID.2016.0199
PMID:28177261
Abstract

In the absence of an effective vaccine, strategies to prevent HIV transmission are urgently needed. Condomless receptive anal intercourse represents a major route of transmission, and efforts are being made to develop strategies, in which potent anti-HIV drugs are formulated for topical application to the rectum before sex. 5P12-RANTES is a promising candidate for such a purpose. It is an analog of the human chemokine RANTES/CCL5, which potently blocks CCR5, the principal coreceptor used by HIV to enter and infect target cells. As a protein, 5P12-RANTES is potentially vulnerable to attack by proteases in the rectal environment. In this study, we tested the stability of 5P12-RANTES on exposure to rectal lavage samples obtained from healthy volunteers, using a sensitive HIV entry inhibition assay as an indicator of stability. Varying levels of inactivating activity toward 5P12-RANTES were detected across the different lavage samples. Analysis of even the most aggressive samples indicated that protease activity in the rectal environment is unlikely to impact on the anti-HIV activity of 5P12-RANTES when applied pericoitally at the envisaged clinical dose (1 mM). This study indicates that 5P12-RANTES has adequate stability for further development as an HIV prevention drug for rectal use.

摘要

在缺乏有效疫苗的情况下,迫切需要预防艾滋病毒传播的策略。无保护的接受性肛交是主要的传播途径,目前正在努力制定相关策略,即在性行为前将强效抗艾滋病毒药物制成直肠局部应用制剂。5P12-RANTES是实现这一目的的一个有前景的候选药物。它是人类趋化因子RANTES/CCL5的类似物,能有效阻断CCR5,而CCR5是艾滋病毒进入和感染靶细胞所使用的主要共受体。作为一种蛋白质,5P12-RANTES在直肠环境中可能易受蛋白酶攻击。在本研究中,我们使用灵敏的艾滋病毒进入抑制试验作为稳定性指标,检测了5P12-RANTES在暴露于从健康志愿者获得的直肠灌洗样本时的稳定性。在不同的灌洗样本中检测到了对5P12-RANTES不同程度的失活活性。对即使是最具侵袭性的样本进行分析表明,当按照设想的临床剂量(1 mM)在性交时应用5P12-RANTES时,直肠环境中的蛋白酶活性不太可能影响其抗艾滋病毒活性。本研究表明,5P12-RANTES具有足够的稳定性,可进一步开发作为直肠用艾滋病毒预防药物。

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