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新型组蛋白去乙酰化酶抑制剂 CG05 和 CG06 可有效重新激活潜伏感染的 HIV-1。

Novel histone deacetylase inhibitors CG05 and CG06 effectively reactivate latently infected HIV-1.

机构信息

Division of AIDS, Center for Immunology and Pathology, Korea National Institute of Health, 194 Tongillo, Eunpyung-gu, Seoul, Republic of Korea.

出版信息

AIDS. 2010 Feb 20;24(4):609-11. doi: 10.1097/QAD.0b013e328333bfa1.

Abstract

Histone deacetylase plays an important role in HIV latency. Novel histone deacetylase inhibitors, CG05 and CG06, were evaluated for their roles in HIV latency using ACH2 cells. Both inhibitors were highly efficient in reactivation of provirus and exerted lesser toxicity compared with other known histone deacetylase inhibitors. Histone acetylation increased when proviruses were reactivated by the compounds. These new inhibitors may contribute to the reduction of the HIV reservoir when used in conjunction with highly active antiretroviral therapy.

摘要

组蛋白去乙酰化酶在 HIV 潜伏期发挥着重要作用。新型组蛋白去乙酰化酶抑制剂 CG05 和 CG06 被用于评价其在 ACH2 细胞中对 HIV 潜伏期的作用。与其他已知的组蛋白去乙酰化酶抑制剂相比,这两种抑制剂在激活前病毒方面非常有效,且毒性更小。当化合物激活前病毒时,组蛋白乙酰化增加。当与高效抗逆转录病毒疗法联合使用时,这些新型抑制剂可能有助于减少 HIV 储存库。

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