• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[人类免疫缺陷病毒进入细胞的机制及治疗可能性]

[HIV entry into the cells--mechanisms and therapeutic possibilities].

作者信息

Briz Verónica, Poveda Eva, Soriano Vicente

机构信息

Servicio de Enfermedades Infecciosas, Hospital Carlos III, Madrid, Spain.

出版信息

Med Clin (Barc). 2006 Mar 11;126(9):341-8. doi: 10.1157/13085735.

DOI:10.1157/13085735
PMID:16650368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7131321/
Abstract

Human immunodeficiency virus (HIV) entry into cells is the first step in the viral replication cycle, which has been explored as a new therapeutic target. A better knowledge of the mechanisms involved in the entry process has led to the development of agents, which may inhibit each of the different steps of the viral entry process: attachment of the gp120 to the CD4 cell receptor; binding of the gp120 to CCR5 or CXCR4 coreceptors; and the fusion of viral and cell membranes. Entry inhibitors are the latest family of antiretroviral compounds, being enfuvirtide, a fusion inhibitor, the first approved. Several other entry inhibitors are currently in clinical development and hopefully soon will be part of the therapeutic armamentarium against HIV.

摘要

人类免疫缺陷病毒(HIV)进入细胞是病毒复制周期的第一步,这已被作为一个新的治疗靶点进行研究。对病毒进入过程中涉及的机制有了更深入的了解,促使了一些药物的研发,这些药物可能会抑制病毒进入过程的各个不同步骤:gp120与CD4细胞受体的结合;gp120与CCR5或CXCR4共受体的结合;以及病毒膜与细胞膜的融合。进入抑制剂是最新一类抗逆转录病毒化合物,恩夫韦肽作为一种融合抑制剂是首个被批准的药物。目前还有其他几种进入抑制剂正在进行临床开发,有望很快成为对抗HIV的治疗手段之一。

相似文献

1
[HIV entry into the cells--mechanisms and therapeutic possibilities].[人类免疫缺陷病毒进入细胞的机制及治疗可能性]
Med Clin (Barc). 2006 Mar 11;126(9):341-8. doi: 10.1157/13085735.
2
New advances in HIV entry inhibitors development.HIV进入抑制剂研发的新进展。
Curr Drug Targets Infect Disord. 2004 Dec;4(4):339-55. doi: 10.2174/1568005043340498.
3
HIV entry and fusion inhibitors.HIV进入和融合抑制剂。
Expert Opin Emerg Drugs. 2004 May;9(1):1-7. doi: 10.1517/eoed.9.1.1.32950.
4
Virus entry as a target for anti-HIV intervention.作为抗HIV干预靶点的病毒进入过程
Curr Med Chem. 2003 Sep;10(17):1617-32. doi: 10.2174/0929867033457098.
5
[Viral entry as therapeutic target. Current situation of entry inhibitors].[以病毒进入为治疗靶点。进入抑制剂的现状]
Enferm Infecc Microbiol Clin. 2008 Oct;26 Suppl 11:5-11. doi: 10.1016/s0213-005x(08)76557-1.
6
Development of anti-HIV agents targeting dynamic supramolecular mechanism: entry and fusion inhibitors based on CXCR4/CCR5 antagonists and gp41-C34-remodeling peptides.靶向动态超分子机制的抗HIV药物研发:基于CXCR4/CCR5拮抗剂和gp41-C34重塑肽的进入和融合抑制剂
Curr HIV Res. 2005 Oct;3(4):289-301. doi: 10.2174/157016205774370429.
7
Kinetic factors control efficiencies of cell entry, efficacies of entry inhibitors, and mechanisms of adaptation of human immunodeficiency virus.动力学因素控制着人类免疫缺陷病毒的细胞进入效率、进入抑制剂的效力以及适应机制。
J Virol. 2005 Apr;79(7):4347-56. doi: 10.1128/JVI.79.7.4347-4356.2005.
8
HIV entry inhibitors: progress in development and application.HIV进入抑制剂:开发与应用进展
Yao Xue Xue Bao. 2010 Feb;45(2):131-40.
9
Activity of the HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068, against CD4-independent viruses and HIV-1 envelopes resistant to other entry inhibitors.HIV-1 附着抑制剂 BMS-626529(前药 BMS-663068 的活性成分)对 CD4 非依赖性病毒和对其他进入抑制剂耐药的 HIV-1 包膜的活性。
Antimicrob Agents Chemother. 2013 Sep;57(9):4172-80. doi: 10.1128/AAC.00513-13. Epub 2013 Jun 17.
10
Reversible and efficient activation of HIV-1 cell entry by a tyrosine-sulfated peptide dissects endocytic entry and inhibitor mechanisms.酪氨酸硫酸化肽可逆且高效地激活 HIV-1 细胞进入,揭示了内吞进入和抑制剂作用机制。
J Virol. 2014 Apr;88(8):4304-18. doi: 10.1128/JVI.03447-13. Epub 2014 Jan 29.

本文引用的文献

1
Enfuvirtide is active against HIV type 1 group O.恩夫韦肽对1型艾滋病毒O组有活性。
AIDS Res Hum Retroviruses. 2005 Jun;21(6):583-5. doi: 10.1089/aid.2005.21.583.
2
The appealing story of HIV entry inhibitors : from discovery of biological mechanisms to drug development.HIV进入抑制剂的引人入胜的故事:从生物学机制的发现到药物研发。
Drugs. 2005;65(7):879-904. doi: 10.2165/00003495-200565070-00001.
3
New approaches toward anti-HIV chemotherapy.抗艾滋病病毒化疗的新方法。
J Med Chem. 2005 Mar 10;48(5):1297-313. doi: 10.1021/jm040158k.
4
The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor.873140是一种有效的变构非竞争性HIV进入抑制剂,其基于CCR5受体的作用机制。
Mol Pharmacol. 2005 Apr;67(4):1268-82. doi: 10.1124/mol.104.008565. Epub 2005 Jan 11.
5
Characterization of determinants of genotypic and phenotypic resistance to enfuvirtide in baseline and on-treatment HIV-1 isolates.基线和治疗期间HIV-1分离株中恩夫韦肽基因型和表型耐药性决定因素的特征分析
AIDS. 2004 Sep 3;18(13):1787-94. doi: 10.1097/00002030-200409030-00007.
6
Spirodiketopiperazine-based CCR5 inhibitor which preserves CC-chemokine/CCR5 interactions and exerts potent activity against R5 human immunodeficiency virus type 1 in vitro.基于螺二酮哌嗪的CCR5抑制剂,其保留CC趋化因子/CCR5相互作用并在体外对R5型人类免疫缺陷病毒1型发挥强效活性。
J Virol. 2004 Aug;78(16):8654-62. doi: 10.1128/JVI.78.16.8654-8662.2004.
7
Evolution of genotypic and phenotypic resistance to Enfuvirtide in HIV-infected patients experiencing prolonged virologic failure.在经历长期病毒学失败的HIV感染患者中,对恩夫韦肽的基因型和表型耐药性的演变。
J Med Virol. 2004 Sep;74(1):21-8. doi: 10.1002/jmv.20141.
8
Resistance to enfuvirtide, the first HIV fusion inhibitor.对恩夫韦肽(首个HIV融合抑制剂)的耐药性。
J Antimicrob Chemother. 2004 Aug;54(2):333-40. doi: 10.1093/jac/dkh330. Epub 2004 Jul 1.
9
Are fusion inhibitors active against all HIV variants?融合抑制剂对所有HIV变体都有活性吗?
AIDS Res Hum Retroviruses. 2004 Mar;20(3):347-8. doi: 10.1089/088922204322996590.
10
Susceptibility of HIV-2, SIV and SHIV to various anti-HIV-1 compounds: implications for treatment and postexposure prophylaxis.HIV-2、猴免疫缺陷病毒(SIV)和猿猴-人免疫缺陷病毒(SHIV)对各种抗HIV-1化合物的敏感性:对治疗和暴露后预防的意义。
Antivir Ther. 2004 Feb;9(1):57-65.