Mori Luisa, Valente Susana T
Department of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL, USA.
Methods Mol Biol. 2022;2407:391-428. doi: 10.1007/978-1-0716-1871-4_26.
The majority of virally suppressed individuals will experience rapid viral rebound upon antiretroviral therapy (ART) interruption, providing a strong rationale for the development of cure strategies. Moreover, despite ART virological control, HIV infection is still associated with chronic immune activation, inflammation, comorbidities, and accelerated aging. These effects are believed to be due, in part, to low-grade persistent transcription and trickling production of viral proteins from the pool of latent proviruses constituting the viral reservoir. In recent years there has been an increasing interest in developing what has been termed a functional cure for HIV. This approach entails the long-term, durable control of viral expression in the absence of therapy, preventing disease progression and transmission, despite the presence of detectable integrated proviruses. One such strategy, the block-and-lock approach for a functional cure, proposes the epigenetic silencing of proviral expression, locking the virus in a profound latent state, from which reactivation is very unlikely. The proof-of-concept for this approach was demonstrated with the use of a specific small molecule targeting HIV transcription. Here we review the principles behind the block-and-lock approach and some of the additional strategies proposed to silence HIV expression.
大多数病毒得到抑制的个体在抗逆转录病毒疗法(ART)中断后会经历病毒快速反弹,这为治愈策略的开发提供了有力依据。此外,尽管ART实现了病毒学控制,但HIV感染仍与慢性免疫激活、炎症、合并症和加速衰老有关。这些影响被认为部分归因于构成病毒储存库的潜伏前病毒库中低水平的持续转录和病毒蛋白的微量产生。近年来,人们对开发所谓的HIV功能性治愈方法越来越感兴趣。这种方法需要在不进行治疗的情况下长期、持久地控制病毒表达,尽管存在可检测到的整合前病毒,但仍能预防疾病进展和传播。一种这样的策略,即功能性治愈的“阻断并锁定”方法,提出对前病毒表达进行表观遗传沉默,将病毒锁定在深度潜伏状态,从这种状态重新激活的可能性非常小。使用一种靶向HIV转录的特定小分子证明了这种方法的概念验证。在这里,我们回顾“阻断并锁定”方法背后的原理以及为沉默HIV表达而提出的一些其他策略。