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评估融合抑制剂 P3 肽作为一种预防女性 HIV 传播的潜在杀微生物剂。

Evaluation of the fusion inhibitor P3 peptide as a potential microbicide to prevent HIV transmission in women.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculdade de Farmácia da Universidade de Lisboa, Lisboa, Portugal.

Centro de Administração e Políticas Públicas (CAPP), Instituto Superior de Ciências Sociais e Políticas (ISCSP) da Universidade de Lisboa, Lisboa, Portugal.

出版信息

PLoS One. 2018 Apr 18;13(4):e0195744. doi: 10.1371/journal.pone.0195744. eCollection 2018.

Abstract

Microbicides are an important strategy for preventing the sexual transmission of HIV but, so far, the most advanced tenofovir-based microbicides have had modest efficacy. This has been related to adherence problems and high prevalence of tenofovir-resistant HIV-1 strains. P3 is a new peptide with potent activity against HIV that may be a good microbicide candidate. In this work P3 was formulated in a gel of hydroxyethyl cellulose and its activity, stability and safety profile in Balb/c mice were evaluated. HIV infection was fully blocked by a 1.5% gel containing P3 at the IC90 (366.4 nM) concentration. The antiviral activity did not change at 4°C during 4 months and at 25, 37 and 65°C for 1 week. P3 was stable and fully functional at acidic pH up to 24h, under different concentrations of hydrogen peroxide and in the presence of genital fluids up to 48h. P3 had no antibacterial activity and did not affect sperm motility and vitality. Finally, P3 didn't cause significant alterations in the vaginal epithelium of Balb/c mice at 0.06 (456.8 μM) and 0.2 mg/day (1522.7 μM) doses. These findings indicate that P3 is an excellent candidate for further development as a microbicide gel for the prevention of HIV transmission in women.

摘要

杀微生物剂是预防 HIV 性传播的重要策略,但迄今为止,最先进的基于替诺福韦的杀微生物剂的疗效有限。这与依从性问题和高流行的替诺福韦耐药 HIV-1 株有关。P3 是一种针对 HIV 具有强大活性的新型肽,可能是一种很好的杀微生物候选药物。在这项工作中,P3 被配制在羟乙基纤维素凝胶中,并在 Balb/c 小鼠中评估了其活性、稳定性和安全性。在 IC90(366.4 nM)浓度下,含有 P3 的 1.5%凝胶可完全阻断 HIV 感染。在 4 个月内,在 4°C 下,在 25、37 和 65°C 下放置 1 周,抗病毒活性均未发生变化。P3 在酸性 pH 值下稳定且功能完整,可维持长达 24 小时,在不同浓度的过氧化氢和存在生殖液的情况下,可维持长达 48 小时。P3 无抗菌活性,不影响精子活力和活力。最后,P3 在 0.06(456.8 μM)和 0.2mg/天(1522.7 μM)剂量下,不会引起 Balb/c 小鼠阴道上皮的显著改变。这些发现表明,P3 是进一步开发作为女性预防 HIV 传播的杀微生物凝胶的优秀候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c6d/5905968/9206d6c912f1/pone.0195744.g001.jpg

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