Latinovic Olga, Kuruppu Janaki, Davis Charles, Le Nhut, Heredia Alonso
Institute of Human Virology, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Clin Med Ther. 2009;1:1497-1510. doi: 10.4137/cmt.s2365.
Sustained inhibition of HIV-1, the goal of antiretroviral therapy, is often impeded by the emergence of viral drug resistance. For patients infected with HIV-1 resistant to conventional drugs from the viral reverse transcriptase and protease inhibitor classes, the recently approved entry and integration inhibitors effectively suppress HIV-1 and offer additional therapeutic options. Entry inhibitors are particularly attractive because, unlike conventional antiretrovirals, they target HIV-1 extracellularly, thereby sparing cells from both viral- and drug-induced toxicities. The fusion inhibitor enfuvirtide and the CCR5 antagonist maraviroc are the first entry inhibitors licensed for patients with drug-resistant HIV-1, with maraviroc restricted to those infected with CCR5-tropic HIV-1 (R5 HIV-1) only. Vicriviroc (another CCR5 antagonist) is in Phase III clinical trials, whereas the CCR5 antibodies PRO 140 and HGS 004 are in early stages of clinical development. Potent antiviral synergy between maraviroc and CCR5 antibodies, coupled with distinct patterns of resistance, suggest their combinations might be particularly effective in patients. In addition, given that oral administration of maraviroc achieves high drug levels in cervicovaginal fluid, combinations of maraviroc and other CCR5 inhibitors could be effective in preventing HIV-1 transmission. Moreover, since CCR5 antagonists prevent rejection of transplanted organs, maraviroc could both suppress HIV-1 and prolong organ survival for the growing number of HIV-1 patients with kidney or liver failure necessitating organ transplantation. Thus, maraviroc offers an important treatment option for patients with drug-resistant R5 HIV-1, who presently account for >50% of drug-resistance cases.
抗逆转录病毒疗法的目标是持续抑制HIV-1,但病毒耐药性的出现常常阻碍这一目标的实现。对于感染了对病毒逆转录酶和蛋白酶抑制剂类传统药物耐药的HIV-1的患者,最近获批的进入和整合抑制剂能有效抑制HIV-1,并提供了更多治疗选择。进入抑制剂特别有吸引力,因为与传统抗逆转录病毒药物不同,它们在细胞外靶向HIV-1,从而使细胞免受病毒和药物诱导的毒性。融合抑制剂恩夫韦肽和CCR5拮抗剂马拉维若为首批被批准用于耐药HIV-1患者的进入抑制剂,其中马拉维若仅适用于感染CCR5嗜性HIV-1(R5 HIV-1)的患者。维立韦罗(另一种CCR5拮抗剂)正处于III期临床试验阶段,而CCR5抗体PRO 140和HGS 004正处于临床开发的早期阶段。马拉维若与CCR5抗体之间强大的抗病毒协同作用,以及不同的耐药模式,表明它们的联合使用可能对患者特别有效。此外,鉴于口服马拉维若可在宫颈阴道液中达到较高的药物水平,马拉维若与其他CCR5抑制剂联合使用可能有效预防HIV-1传播。而且,由于CCR5拮抗剂可防止移植器官的排斥反应,对于越来越多因肾衰竭或肝衰竭而需要器官移植的HIV-1患者,马拉维若既能抑制HIV-1,又能延长器官存活时间。因此,马拉维若为耐药R5 HIV-1患者提供了一种重要的治疗选择,目前这类患者占耐药病例的50%以上。