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抑制剂凋亡蛋白拮抗剂 Debio 1143 是一种有吸引力的 HIV-1 潜伏期逆转候选药物。

The inhibitor apoptosis protein antagonist Debio 1143 Is an attractive HIV-1 latency reversal candidate.

机构信息

Department of Immunology & Microbiology, The Scripps Research Institute, La Jolla, California, United States of America.

Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States of America.

出版信息

PLoS One. 2019 Feb 4;14(2):e0211746. doi: 10.1371/journal.pone.0211746. eCollection 2019.

Abstract

Antiretroviral therapy (ART) suppresses HIV replication, but does not cure the infection because replication-competent virus persists within latently infected CD4+ T cells throughout years of therapy. These reservoirs contain integrated HIV-1 genomes and can resupply active virus. Thus, the development of strategies to eliminate the reservoir of latently infected cells is a research priority of global significance. In this study, we tested efficacy of a new inhibitor of apoptosis protein antagonist (IAPa) called Debio 1143 at reversing HIV latency and investigated its mechanisms of action. Debio 1143 activates HIV transcription via NF-kB signaling by degrading the ubiquitin ligase baculoviral IAP repeat-containing 2 (BIRC2), a repressor of the non-canonical NF-kB pathway. Debio 1143-induced BIRC2 degradation results in the accumulation of NF-κB-inducing kinase (NIK) and proteolytic cleavage of p100 into p52, leading to nuclear translocation of p52 and RELB. Debio 1143 greatly enhances the binding of RELB to the HIV-1 LTR. These data indicate that Debio 1143 activates the non-canonical NF-kB signaling pathway by promoting the binding of RELB:p52 complexes to the HIV-1 LTR, resulting in the activation of the LTR-dependent HIV-1 transcription. Importantly, Debio 1143 reverses viral latency in HIV-1 latent T cell lines. Using knockdown (siRNA BIRC2), knockout (CRIPSR NIK) and proteasome machinery neutralization (MG132) approaches, we found that Debio 1143-mediated HIV latency reversal is BIRC2 degradation- and NIK stabilization-dependent. Debio 1143 also reverses HIV-1 latency in resting CD4+ T cells derived from ART-treated patients or HIV-1-infected humanized mice under ART. Interestingly, daily oral administration of Debio 1143 in cancer patients at well-tolerated doses elicited BIRC2 target engagement in PBMCs and induced a moderate increase in cytokines and chemokines mechanistically related to NF-kB signaling. In conclusion, we provide strong evidences that the IAPa Debio 1143, by initially activating the non-canonical NF-kB signaling and subsequently reactivating HIV-1 transcription, represents a new attractive viral latency reversal agent (LRA).

摘要

抗逆转录病毒疗法(ART)抑制 HIV 复制,但不能治愈感染,因为在多年的治疗过程中,复制能力的病毒仍潜伏在受感染的 CD4+T 细胞中。这些储库包含整合的 HIV-1 基因组,并且可以重新供应活跃的病毒。因此,开发消除潜伏感染细胞库的策略是具有全球意义的研究重点。在这项研究中,我们测试了一种新的凋亡蛋白拮抗剂(IAPa) Debio 1143 逆转 HIV 潜伏期的功效,并研究了其作用机制。Debio 1143 通过降解泛素连接酶杆状病毒 IAP 重复序列 2(BIRC2)来激活 NF-kB 信号转导,从而激活 HIV 转录,BIRC2 是非经典 NF-kB 途径的抑制剂。Debio 1143 诱导的 BIRC2 降解导致 NF-κB 诱导激酶(NIK)的积累和 p100 切割为 p52,导致 p52 和 RELB 核易位。Debio 1143 大大增强了 RELB 与 HIV-1 LTR 的结合。这些数据表明,Debio 1143 通过促进 RELB:p52 复合物与 HIV-1 LTR 的结合来激活非经典 NF-kB 信号通路,从而激活 LTR 依赖性 HIV-1 转录。重要的是,Debio 1143 逆转了 HIV-1 潜伏 T 细胞系中的病毒潜伏期。通过使用 knockdown(siRNA BIRC2)、 knockout(CRIPSR NIK)和蛋白酶体机制中和(MG132)方法,我们发现 Debio 1143 介导的 HIV 潜伏期逆转依赖于 BIRC2 降解和 NIK 稳定。Debio 1143 还可逆转来自接受 ART 治疗的患者或在 ART 下感染 HIV-1 的人类化小鼠的静止 CD4+T 细胞中的 HIV-1 潜伏期。有趣的是,在可耐受剂量下,每日口服给予 Debio 1143 会在 PBMC 中引起 BIRC2 靶标结合,并诱导与 NF-kB 信号相关的细胞因子和趋化因子适度增加。总之,我们提供了强有力的证据表明,IAPa Debio 1143 通过最初激活非经典 NF-kB 信号,随后重新激活 HIV-1 转录,代表了一种新的有吸引力的病毒潜伏期逆转剂(LRA)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b47/6361451/4e7db4c284b2/pone.0211746.g001.jpg

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