Department of Infectious Diseases, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, Aarhus, Denmark.
Department of Infectious Diseases, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, Aarhus, Denmark.
Trends Microbiol. 2016 Feb;24(2):90-97. doi: 10.1016/j.tim.2015.11.003. Epub 2015 Dec 11.
Here, the use of pharmacological agents to reverse HIV-1 latency will be explored as a therapeutic strategy towards a cure. However, while clinical trials of latency-reversing agents LRAs) have demonstrated their ability to increase production of latent HIV-1, such interventions have not had an effect on the size of the latent HIV-1 reservoir. Plausible explanations for this include insufficient host immune responses against virus-expressing cells, the presence of escape mutations in archived virus, or an insufficient scale of latency reversal. Importantly, these early studies of LRAs were primarily designed to investigate their ability to perturb the state of HIV-1 latency; using the absence of an impact on the size of the HIV-1 reservoir to discard their potential inclusion in curative strategies would be erroneous and premature.
在这里,将探讨使用药理学制剂来逆转 HIV-1 潜伏期,以此作为一种治疗方法来实现治愈。然而,尽管逆转潜伏制剂(LRAs)的临床试验已经证明了它们能够增加潜伏 HIV-1 的产生,但这些干预措施并没有对潜伏 HIV-1 储存库的大小产生影响。对此的合理解释包括宿主对表达病毒的细胞的免疫反应不足、储存的病毒存在逃逸突变,或者潜伏逆转的规模不足。重要的是,这些早期的 LRA 研究主要旨在研究它们扰乱 HIV-1 潜伏期状态的能力;如果根据它们对 HIV-1 储存库大小的影响来排除它们在治愈策略中的潜在应用,那将是错误和不成熟的。