Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia; The Peter Doherty Institute of Immunity and Infection, University of Melbourne and Royal Melbourne Hospital, Melbourne, VIC, Australia.
The Peter Doherty Institute of Immunity and Infection, University of Melbourne and Royal Melbourne Hospital, Melbourne, VIC, Australia.
Cell Host Microbe. 2018 Jan 10;23(1):14-26. doi: 10.1016/j.chom.2017.12.004.
Despite the success of antiretroviral therapy (ART), there is currently no HIV cure and treatment is life long. HIV persists during ART due to long-lived and proliferating latently infected CD4+ T cells. One strategy to eliminate latency is to activate virus production using latency reversing agents (LRAs) with the goal of triggering cell death through virus-induced cytolysis or immune-mediated clearance. However, multiple studies have demonstrated that activation of viral transcription alone is insufficient to induce cell death and some LRAs may counteract cell death by promoting cell survival. Here, we review new approaches to induce death of latently infected cells through apoptosis and inhibition of pathways critical for cell survival, which are often hijacked by HIV proteins. Given advances in the commercial development of compounds that induce apoptosis in cancer chemotherapy, these agents could move rapidly into clinical trials, either alone or in combination with LRAs, to eliminate latent HIV infection.
尽管抗逆转录病毒疗法(ART)取得了成功,但目前尚无 HIV 治愈方法,且治疗需要终身进行。由于长寿和增殖的潜伏感染 CD4+T 细胞的存在,HIV 在 ART 期间持续存在。消除潜伏期的一种策略是使用潜伏逆转剂(LRAs)激活病毒产生,其目标是通过病毒诱导的细胞溶解或免疫介导的清除来触发细胞死亡。然而,多项研究表明,仅激活病毒转录不足以诱导细胞死亡,并且一些 LRA 可能通过促进细胞存活来对抗细胞死亡。在这里,我们回顾了通过细胞凋亡和抑制对细胞存活至关重要的途径来诱导潜伏感染细胞死亡的新方法,这些途径经常被 HIV 蛋白劫持。鉴于在癌症化疗中诱导细胞凋亡的化合物的商业开发取得了进展,这些药物可以迅速进入临床试验,单独使用或与 LRA 联合使用,以消除潜伏的 HIV 感染。