Targeting noncoding RNAs to reactivate or eliminate latent HIV reservoirs.

Current opinion in HIV and AIDS Pub Date : 2024-03-01 Epub Date: 2023-12-20 DOI:10.1097/COH.0000000000000838
Nadejda Beliakova-Bethell
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Abstract

Purpose of review: Expression of noncoding RNAs (ncRNAs) is more tissue and cell type-specific than expression of protein-coding genes. Understanding the mechanisms of action of ncRNAs and their roles in HIV replication and latency may inform targets for the latent HIV reservoir reactivation or elimination with high specificity to CD4 + T cells latently infected with HIV.

Recent findings: While the number of studies in the field of ncRNAs and HIV is limited, evidence points to complex interactions between different ncRNAs, protein-coding RNAs, and proteins. Latency-reversing agents modulate the expression of ncRNAs, with some effects being inhibitory for HIV reactivation. An important limitation of basic research on the ncRNA mechanisms of action is the reliance on cell lines. Because of cell type specificity, it is uncertain whether the ncRNAs function similarly in primary cells.

Summary: Comprehensive functional screens to uncover all ncRNAs that regulate HIV expression and the detailed exploration of their mechanisms of action in relevant cell types are needed to identify promising targets for HIV reservoir clearance. Classes of ncRNAs as a whole rather than individual ncRNAs might represent an attractive target for reservoir elimination. Compound screens for latency reversal should factor in the complexity of their effects on ncRNAs.

以非编码 RNA 为目标,重新激活或消除潜伏的 HIV 储库。
综述的目的:与蛋白编码基因的表达相比,非编码 RNA(ncRNA)的表达更具组织和细胞类型特异性。了解 ncRNA 的作用机制及其在 HIV 复制和潜伏过程中的作用,可为潜伏 HIV 库的重新激活或消除目标提供信息,这些目标对潜伏感染 HIV 的 CD4+ T 细胞具有高度特异性:虽然在 ncRNA 和 HIV 领域的研究数量有限,但有证据表明不同的 ncRNA、蛋白编码 RNA 和蛋白质之间存在复杂的相互作用。潜伏期逆转剂可调节 ncRNAs 的表达,其中一些作用可抑制 HIV 的再次激活。ncRNA 作用机制基础研究的一个重要局限是依赖细胞系。由于细胞类型的特异性,目前还不能确定 ncRNA 在原代细胞中是否发挥类似的作用。总结:需要进行全面的功能筛选,以发现所有调控 HIV 表达的 ncRNA,并详细探索它们在相关细胞类型中的作用机制,从而确定有希望清除 HIV 库的靶点。ncRNA类作为一个整体而不是单个ncRNA可能是清除病毒库的一个有吸引力的靶点。逆转潜伏期的化合物筛选应考虑其对 ncRNA 影响的复杂性。
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