Division of Infectious Diseases, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Center for Pathogen Genomics and Microbial Evolution, Havey Institute for Global Health, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
PLoS Pathog. 2024 Sep 11;20(9):e1012083. doi: 10.1371/journal.ppat.1012083. eCollection 2024 Sep.
The persistence of HIV-1 in long-lived latent reservoirs during suppressive antiretroviral therapy (ART) remains one of the principal barriers to a functional cure. Blocks to transcriptional elongation play a central role in maintaining the latent state, and several latency reversal strategies focus on the release of positive transcription elongation factor b (P-TEFb) from sequestration by negative regulatory complexes, such as the 7SK complex and BRD4. Another major cellular reservoir of P-TEFb is in Super Elongation Complexes (SECs), which play broad regulatory roles in host gene expression. Still, it is unknown if the release of P-TEFb from SECs is a viable latency reversal strategy. Here, we demonstrate that the SEC is not required for HIV-1 replication in primary CD4+ T cells and that a small molecular inhibitor of the P-TEFb/SEC interaction (termed KL-2) increases viral transcription. KL-2 acts synergistically with other latency reversing agents (LRAs) to reactivate viral transcription in several cell line models of latency in a manner that is, at least in part, dependent on the viral Tat protein. Finally, we demonstrate that KL-2 enhances viral reactivation in peripheral blood mononuclear cells (PBMCs) from people living with HIV (PLWH) on suppressive ART, most notably in combination with inhibitor of apoptosis protein antagonists (IAPi). Taken together, these results suggest that the release of P-TEFb from cellular SECs may be a novel route for HIV-1 latency reactivation.
在抑制性抗逆转录病毒疗法 (ART) 期间,HIV-1 长期潜伏在储库中仍然是功能性治愈的主要障碍之一。转录延伸的阻滞在维持潜伏状态中起着核心作用,几种潜伏逆转策略集中在将正转录延伸因子 b (P-TEFb) 从 7SK 复合物和 BRD4 等负调控复合物的隔离中释放出来。P-TEFb 的另一个主要细胞储库是在超级延伸复合物 (SECs) 中,SEC 在宿主基因表达中发挥广泛的调节作用。然而,目前尚不清楚 P-TEFb 从 SEC 中的释放是否是一种可行的潜伏逆转策略。在这里,我们证明 SEC 对于原代 CD4+ T 细胞中的 HIV-1 复制不是必需的,并且 P-TEFb/SEC 相互作用的小分子抑制剂 (称为 KL-2) 可增加病毒转录。KL-2 与其他潜伏逆转剂 (LRAs) 协同作用,以重新激活几种潜伏细胞模型中的病毒转录,其作用至少部分依赖于病毒 Tat 蛋白。最后,我们证明 KL-2 增强了接受抑制性 ART 的 HIV 感染者 (PLWH) 的外周血单核细胞 (PBMC) 中的病毒重新激活,尤其是与凋亡蛋白抑制剂 (IAPi) 联合使用时。综上所述,这些结果表明,P-TEFb 从细胞 SEC 中的释放可能是 HIV-1 潜伏再激活的一种新途径。