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抗逆转录病毒治疗的新靶点。

Novel targets for anti-retroviral therapy.

机构信息

HPA West Midlands Public Health Laboratory, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, United Kingdom.

出版信息

J Infect. 2009 Dec;59(6):377-86. doi: 10.1016/j.jinf.2009.09.014. Epub 2009 Oct 6.

Abstract

Novel targets for the management of HIV infection have become increasingly relevant in view of extensive drug resistance, side effects and high pill burden of some of the conventional anti-retroviral agents. Structure based drug design using X-ray crystallography, nuclear magnetic resonance, and mass spectrometry have lead to the identification of novel class of drugs targeting new stages of HIV life cycle. These agents include chemokine receptor antagonists and the integrase inhibitors which were recently approved for HIV treatment, as well as numerous other agents directed to previously untested targets such as the maturation inhibitors, zinc finger inhibitors, pharmacological CDK inhibitors, Tat-TAR interaction inhibitors, anti-CD4 monoclonal antibody, antisense oligonucleotides, oxidisers of the HIV lipid envelope and agents acting on the proviral DNA. Use of new agents with novel mechanism of action requires the development of new laboratory assays to detect viral tropism and new resistance mutations. Despite the new developments providing hope to patients and clinicians in the fights against HIV, eradication of the disease still remains elusive. This review discusses issues surrounding the development of these new agents.

摘要

鉴于某些传统抗逆转录病毒药物的广泛耐药性、副作用和高剂量负担,针对 HIV 感染管理的新靶点变得越来越重要。基于结构的药物设计使用 X 射线晶体学、核磁共振和质谱分析,已经确定了针对 HIV 生命周期新阶段的新型药物类别。这些药物包括趋化因子受体拮抗剂和整合酶抑制剂,它们最近已被批准用于 HIV 治疗,以及许多针对以前未经测试的靶点的其他药物,如成熟抑制剂、锌指抑制剂、药理学 CDK 抑制剂、Tat-TAR 相互作用抑制剂、抗 CD4 单克隆抗体、反义寡核苷酸、HIV 脂质包膜氧化剂和作用于前病毒 DNA 的药物。新型作用机制的新药物的使用需要开发新的实验室检测方法来检测病毒嗜性和新的耐药突变。尽管新的发展为患者和临床医生抗击 HIV 带来了希望,但该疾病的根除仍然难以实现。本文综述了这些新药物开发所面临的问题。

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