Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón, Madrid, Spain ; Instituto de Investigación Sanitaria del Gregorio Marañón, Madrid, Spain ; Networking Research Center on Bioengineering, Biomaterials and Nanomedicine, (CIBER-BBN), Madrid, Spain.
Networking Research Center on Bioengineering, Biomaterials and Nanomedicine, (CIBER-BBN), Madrid, Spain ; Dendrimers for Biomedical Applications Group (BioInDen), University of Alcalá, Madrid, Spain.
Int J Nanomedicine. 2014 Jul 29;9:3591-600. doi: 10.2147/IJN.S62673. eCollection 2014.
Self-administered topical microbicides or oral preexposure prophylaxis could be very helpful tools for all risk groups to decrease the human immunodeficiency virus (HIV)-1 infection rates. Up until now, antiretrovirals (ARVs) have been the most advanced microbicide candidates. Nevertheless, the majority of clinical trials has failed in HIV-1 patients. Nanotechnology offers suitable approaches to develop novel antiviral agents. Thereby, new nanosystems, such as carbosilane dendrimers, have been shown to be safe and effective compounds against HIV with great potential as topical microbicides. In addition, because most of the attempts to develop effective topical microbicides were unsuccessful, combinatorial strategies could be a valid approach when designing new microbicides. We evaluated various combinations of anionic carbosilane dendrimers with sulfated (G3-S16) and naphthyl sulfonated (G2-NF16) ended groups with different ARVs against HIV-1 infection. The G3-S16 and G2-NF16 dendrimers showed a synergistic or additive activity profile with zidovudine, efavirenz, and tenofovir in the majority of the combinations tested against the X4 and R5 tropic HIV-1 in cell lines, as well as in human primary cells. Therefore, the combination of ARVs and polyanionic carbosilane dendrimers enhances the antiviral potency of the individual compounds, and our findings support further clinical research on combinational approaches as potential microbicides to block the sexual transmission of HIV-1.
自我管理的局部外用杀微生物剂或口服暴露前预防可能是所有风险群体非常有用的工具,可以降低人类免疫缺陷病毒 (HIV)-1 的感染率。到目前为止,抗逆转录病毒药物 (ARV) 一直是最先进的杀微生物剂候选药物。然而,大多数临床试验都在 HIV-1 患者中失败了。纳米技术为开发新型抗病毒药物提供了合适的方法。因此,新型纳米系统,如碳硅烷树状大分子,已被证明是安全有效的抗 HIV 化合物,具有作为局部杀微生物剂的巨大潜力。此外,由于大多数开发有效局部杀微生物剂的尝试都不成功,因此在设计新的杀微生物剂时,组合策略可能是一种有效的方法。我们评估了不同阴离子碳硅烷树状大分子与带磺酸基(G3-S16)和萘基磺酸基(G2-NF16)端基的与不同 ARV 联合应用对 HIV-1 感染的抑制作用。在针对 X4 和 R5 嗜性 HIV-1 的细胞系以及人原代细胞中,G3-S16 和 G2-NF16 树状大分子与齐多夫定、依非韦伦和替诺福韦的大多数组合显示出协同或相加的活性谱。因此,ARV 和聚阴离子碳硅烷树状大分子的联合应用增强了单个化合物的抗病毒效力,我们的研究结果支持进一步研究联合应用作为潜在的杀微生物剂来阻断 HIV-1 的性传播的组合方法。