Stellbrink Hans-Jürgen
Infektionsmedizinisches Centrum Hamburg ICH, Grindelallee 35, 20146 Hamburg, Germany.
Eur J Med Res. 2007 Oct 15;12(9):483-95.
Drug development in the field of HIV treatment is rapid. New nucleoside analogues (NRTI), non-nucleoside analogue reverse transcriptase inhibitors (NNRTI), and protease inhibitors (PI) are currently being investigated in human trials. Furthermore, inhibitors of HIV attachment, fusion and integrase with novel modes of action are being developed, which offer new perspectives for the goal of a normalization of life-expectancy in HIV-infected individuals. The most advanced compounds likely to become licensed soon include the NNRTIs rilpivirine and etravirine, the integrase inhibitors raltegravir and elvitegravir, and maraviroc and vicriviroc, novel inhibitors of the CCR5 chemokine receptor, which functions as the major coreceptor for HIV-1.
艾滋病治疗领域的药物研发进展迅速。新型核苷类似物(NRTI)、非核苷类逆转录酶抑制剂(NNRTI)和蛋白酶抑制剂(PI)目前正在人体试验中进行研究。此外,具有新型作用模式的HIV附着、融合和整合酶抑制剂也在研发中,这为实现HIV感染者预期寿命正常化的目标提供了新的前景。最有可能很快获得许可的先进化合物包括NNRTIs类的利匹韦林和依曲韦林、整合酶抑制剂拉替拉韦和埃替拉韦,以及CCR5趋化因子受体新型抑制剂马拉维罗和维克维罗,CCR5趋化因子受体是HIV-1的主要共受体。