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HIV-1整合酶抑制剂耐药研究进展 被引量:5

Advances in drug resistance of HIV-1 integrase inhibitors
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摘要 在艾滋病病毒(HIV)整个生命周期中,整合酶是病毒复制整合到宿主细胞脱氧核糖核酸(DNA)过程中十分重要的酶。它可以催化病毒的互补DNA整合进入宿主基因组中。由于整合酶抑制剂的高耐药屏障和低毒性,因此以雷替格韦(RAL)为代表的整合酶抑制剂在治疗HIV中十分具有前景。与其他抗HIV药物类似,整合酶抑制剂也不可避免地会出现耐药的情况。本综述主要总结目前关于整合酶抑制剂耐药的研究情况。 Integrase is a very important enzyme for virus replication and integration into host cell DNA during the whole life cycle of HIV.It catalyzes the integration of the virus’s cDNA into the host genome.Since there are no integrase functional analogues in human cells,integrase inhibitors represented by RAL have great potential in the treatment of HIV.Like other anti-HIV drugs,integrase inhibitors will inevitably show drug resistance.This review mainly summarizes the current research on integrase inhibitor resistance.
作者 谢小慧 于凤婷 张霞 赵红心 张福杰 XIE Xiaohui;YU Fengting;ZHANG Xia;ZHAO Hongxin;ZHANG Fujie(Ditan Teaching Hospital,Peking University,Beijing 100015,China;Beijing Ditan Hospital,Capital Medical University,Beijing 100015;Medical Laboratory Science,Weifang Medical College,Weifang 261053,Shandong)
出处 《中国艾滋病性病》 CAS CSCD 北大核心 2020年第8期900-902,F0003,共4页 Chinese Journal of Aids & STD
基金 儿童艾滋病适宜治疗和预防策略研究与应用(2018ZX10302-102) 北京市医管中心项目(DFL20191802) Supported by John C.Martin Foundation。
关键词 1型艾滋病病毒 整合酶 耐药 基因型耐药检测 human immunodeficiencyvirus-1 integrase inhibitor drug resistance genotype resistance testing
作者简介 第一作者简介:谢小慧(1993-),女,硕士在读,主要研究传染病的诊断与治疗。Email:17732315640@163.com;通信作者:张福杰,教授/博士生导师,Email:treatment@chinaaids.cn。
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  • 1高彦杰,刘英杰,姜树林.国内HIV高危人群队列研究现状[J].慢性病学杂志,2013,13(3):231-236. 被引量:7
  • 2Xiao-huiMA Xiao-yiZHANG Jian-junTAN Wei-zuCHEN Cun-xinWANG.Exploring binding mode for styrylquinoline HIV-1 integrase inhibitors using comparative molecular field analysis and docking studies[J].Acta Pharmacologica Sinica,2004,25(7):950-958. 被引量:3
  • 3傅婷婷,倪孟祥.核苷类抗艾滋病药物研发近况[J].药学进展,2007,31(5):211-216. 被引量:11
  • 4ZHENG Rong-lan, JENKINS T M, CRAIGIE R. Zinc folds the N-terminal domain of HTV- 1 integrase, promotes multimerization, and enhances catalytic activity [J]. Biochemistry, 1996,93 : 13659 - 13664.
  • 5GOLDGUR Y, DYDA F, HICKMAN A B, et al. Three new structures of the core domine of HIV- 1 integrase:An activate site that binds magnesium[J]. Biochemistry, 1998,95:9150 - 9154.
  • 6KEHLENBECK S, BETZ U, BIRKMANN A, et al. Dihydroxythiophenes are novel potent inhibitors of human immunodeficiency virus integrase with a diketo acid-like pharmacophore [ J ]. Virology, 2006, 80: 6883 - 6894.
  • 7JOHNSON A A, SANTOS W, PAIS G C G, et al. Integration requires a specific interaction of the donor DNA terminal 5'-cytosine with glutamine 148 of the HIV-1 integrase flexible loop[ J]. Biological chemistry ,2006,281:461 - 467.
  • 8DIAMOND T L, BUSHMAN F D. Division of labor within human immunodeficiency virus integrase complexes:Determinant of catalisis and target DNA capture[ J]. Virology ,2005,79 : 15376 - 15387.
  • 9PANDEY K K, SINHA S, GRANDGENETT D P. Transcriptional coactivator LEDGF p75 modulates human immunodeficiency virus type 1 integrase-mediated concerted integration [ J ]. Virology, 2007, 81 : 3969 - 3979.
  • 10HAYOUKA Z, ROSENBLUH J, LEVIN A, et al. Inhibiting HIV-1 integrase by shifting its oligomerization equilibrium [J]. PNAS ,2007 ,104 : 8316 - 8321.

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