UNC HIV Cure Center, Institute of Global Health and Infectious Diseases, United States.
UNC HIV Cure Center, Institute of Global Health and Infectious Diseases, United States; Department of Biochemistry and Biophysics, The University of North Carolina at Chapel Hill Chapel Hill, NC 27599-7042, United States.
EBioMedicine. 2021 Jan;63:103159. doi: 10.1016/j.ebiom.2020.103159. Epub 2020 Dec 16.
HIV cure is thwarted by the presence of quiescent yet replication competent HIV-1 (HIV). Antiretroviral therapy (ART) is unable to eradicate reservoirs, and upon cessation of ART, HIV will rebound. This review encompasses the curative strategies of HIV in the context of NF-κB sub-pathways that are currently exploited and demonstrate promise in the disruption of latent HIV. Canonical NF-κB signaling has long been established to drive HIV proviral expression while noncanonical NF-κB signaling, a novel and perhaps more desirable mechanism of latency reversal due to its unique characteristics, has recently been shown to also promote HIV expression from latency. Furthermore, we discuss the previously unrecognized upstream signaling of NF-κB as a new avenue for exploration of a functional cure of HIV.
HIV 治愈受到潜伏但具有复制能力的 HIV-1(HIV)的存在的阻碍。抗逆转录病毒疗法(ART)无法消除储库,一旦停止 ART,HIV 就会反弹。本综述涵盖了 NF-κB 亚途径中 HIV 的治疗策略,这些策略目前正在被利用,并在破坏潜伏 HIV 方面显示出前景。经典 NF-κB 信号通路早已被确立为驱动 HIV 前病毒表达,而非经典 NF-κB 信号通路是一种新的、可能更理想的潜伏逆转机制,因为其独特的特性,最近也被证明可以促进潜伏 HIV 的表达。此外,我们还讨论了 NF-κB 的以前未被认识到的上游信号,作为探索 HIV 功能性治愈的新途径。