Svensson J Peter
Department of Biosciences and Nutrition, Karolinska Institutet (KI), Huddinge, Sweden.
Front Cell Infect Microbiol. 2021 May 7;11:668637. doi: 10.3389/fcimb.2021.668637. eCollection 2021.
The Human Immunodeficiency Virus type 1 (HIV-1) integrates in the host genome as a provirus resulting in a long-lived reservoir of infected CD4 cells. As a provirus, HIV-1 has several aspects in common with an oncogene. Both the HIV-1 provirus and oncogenes only cause disease when expressed. A successful cure of both cancer and HIV-1 includes elimination of all cells with potential to regenerate the disease. For over two decades, epigenetic drugs developed against cancer have been used in the HIV-1 field to modulate the state of the proviral chromatin. Cells with an intact HIV-1 provirus exist in three states of infection: productive, inducible latent, and non-inducible latent. Here focus is on HIV-1, transcription control and chromatin structure; how the inducible proviruses are maintained in a chromatin structure that allows reactivation of transcription; and how transcription switches between different stages to allow for an abundance of different transcripts from a single promoter. Recently it was shown that a functional cure of HIV can be achieved by encapsulating all intact HIV-1 proviruses in heterochromatin, giving hope that epigenetic interventions may be used to end the HIV-1 epidemic.
1型人类免疫缺陷病毒(HIV-1)作为前病毒整合到宿主基因组中,导致受感染的CD4细胞形成长期存在的储存库。作为一种前病毒,HIV-1在几个方面与癌基因有共同之处。HIV-1前病毒和癌基因只有在表达时才会引发疾病。成功治愈癌症和HIV-1都包括消除所有有可能使疾病再生的细胞。二十多年来,针对癌症开发的表观遗传药物已被用于HIV-1领域,以调节前病毒染色质的状态。带有完整HIV-1前病毒的细胞存在于三种感染状态:有生产性的、可诱导潜伏的和不可诱导潜伏的。这里重点关注HIV-1、转录控制和染色质结构;可诱导前病毒如何维持在允许转录重新激活的染色质结构中;以及转录如何在不同阶段之间切换,以便从单个启动子产生大量不同的转录本。最近有研究表明,通过将所有完整的HIV-1前病毒包裹在异染色质中,可以实现HIV的功能性治愈,这让人们看到表观遗传干预可能用于终结HIV-1流行的希望。