Agrawal Lokesh, Lu Xihua, Jin Qingwen, Alkhatib Ghalib
Department of Microbiology & Immunology and the Walther Cancer Institute, Indiana University School of Medicine, Medical Science Building, 635 Barnhill Drive, Rm#420, Indianapolis, IN 46202, USA.
Curr Pharm Des. 2006;12(16):2031-55. doi: 10.2174/138161206777442100.
Although combinations of drugs that target the HIV reverse transcriptase and protease enzymes have clearly revolutionized the treatment of HIV/AIDS, problems with these agents, such as viral escape mutants, persistence of viral reservoirs, poor patient compliance due to complicated regimens, and toxic side effects, have emphasized the need for development of new drugs with novel mechanisms of action, as well as an HIV vaccine. Recently two new classes of drugs have been identified that interfere with the membrane fusion reaction required for HIV entry of target cells. Two such agents, T-20 (enfuvirtide) and T-1249, which have been approved by the Food and Drug Administration (FDA), block the action of the fusogenic envelope glycoprotein gp41. Others target the HIV coreceptors CCR5 and CXCR4, and are now in clinical trials. Also under development are novel agents that target the HIV integrase and HIV regulatory gene products as well as immunomodulators such as IL-12 and IL-2. This article will focus on these and other novel approaches to HIV therapeutics.
尽管针对HIV逆转录酶和蛋白酶的联合药物疗法已显著革新了HIV/AIDS的治疗,但这些药物存在一些问题,如病毒逃逸突变体、病毒储存库持续存在、治疗方案复杂导致患者依从性差以及毒副作用等,这凸显了开发具有新作用机制的新药以及HIV疫苗的必要性。最近已确定了两类新型药物,它们可干扰HIV进入靶细胞所需的膜融合反应。两种此类药物,即已获美国食品药品监督管理局(FDA)批准的T-20(恩夫韦肽)和T-1249,可阻断融合性包膜糖蛋白gp41的作用。其他药物则靶向HIV共受体CCR5和CXCR4,目前正处于临床试验阶段。此外,还有一些新型药物正在研发中,它们靶向HIV整合酶和HIV调节基因产物以及免疫调节剂,如IL-12和IL-2。本文将聚焦于这些以及其他治疗HIV的新方法。