Hartman Tracy L, Buckheit Robert W
Anti-Infective Research Department, ImQuest BioSciences, Inc., 7340 Executive Way, Suite R, Frederick, MD 21704, USA.
Mol Biol Int. 2012;2012:401965. doi: 10.1155/2012/401965. Epub 2012 Jul 10.
During the past three decades, over thirty-five anti-HIV-1 therapies have been developed for use in humans and the progression from monotherapeutic treatment regimens to today's highly active combination antiretroviral therapies has had a dramatic impact on disease progression in HIV-1-infected individuals. In spite of the success of AIDS therapies and the existence of inhibitors of HIV-1 reverse transcriptase, protease, entry and fusion, and integrase, HIV-1 therapies still have a variety of problems which require continued development efforts to improve efficacy and reduce toxicity, while making drugs that can be used throughout both the developed and developing world, in pediatric populations, and in pregnant women. Highly active antiretroviral therapies (HAARTs) have significantly delayed the progression to AIDS, and in the developed world HIV-1-infected individuals might be expected to live normal life spans while on lifelong therapies. However, the difficult treatment regimens, the presence of class-specific drug toxicities, and the emergence of drug-resistant virus isolates highlight the fact that improvements in our therapeutic regimens and the identification of new and novel viral and cellular targets for therapy are still necessary. Antiretroviral therapeutic strategies and targets continue to be explored, and the development of increasingly potent molecules within existing classes of drugs and the development of novel strategies are ongoing.
在过去三十年中,已研发出三十五种以上用于人类的抗HIV-1疗法,从单一疗法治疗方案发展到如今的高效联合抗逆转录病毒疗法,对HIV-1感染者的疾病进展产生了巨大影响。尽管艾滋病疗法取得了成功,并且存在HIV-1逆转录酶、蛋白酶、进入和融合以及整合酶的抑制剂,但HIV-1疗法仍存在各种问题,需要持续开展研发工作以提高疗效并降低毒性,同时研发出可在发达国家和发展中国家、儿科人群以及孕妇中使用的药物。高效抗逆转录病毒疗法(HAARTs)显著延缓了艾滋病的进展,在发达国家,感染HIV-1的个体在接受终身治疗的情况下可能有望过上正常寿命。然而,复杂的治疗方案、特定类别药物毒性的存在以及耐药病毒株的出现凸显了一个事实,即我们仍需改进治疗方案,并确定新的病毒和细胞治疗靶点。抗逆转录病毒治疗策略和靶点仍在不断探索,现有药物类别中效力更强的分子的研发以及新策略的开发也在持续进行。