• 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

在铁过载情况下,铁螯合作为治疗HIV与结核分枝杆菌合并感染的方法。

Iron chelation as therapy for HIV and Mycobacterium tuberculosis co-infection under conditions of iron overload.

作者信息

Meyer Debra

机构信息

Department of Biochemistry, University of Johannesburg, P.O. Box 524 Auckland Park 2006, Gauteng Province, South Africa.

出版信息

Curr Pharm Des. 2006;12(16):1943-7. doi: 10.2174/138161206777442164.

DOI:10.2174/138161206777442164
PMID:16787239
Abstract

Iron chelators, as treatment for conditions of iron overload, have implications for AIDS and tuberculosis (TB) since excess iron in the system assists HIV and Mycobacterium tuberculosis (M.tb) multiplication. Excess iron, especially due to dietary habits, is almost as common in sub-Saharan Africa as infections by the two organisms. That HIV and M.tb influence each other's replication during co-infection is well established, but in vitro evaluations of concurrent infection of the two under conditions of iron overload and determining whether chelators reverse the effect, are limited. This review provides brief commentary on the possibility of iron chelators presently in clinical use influencing simultaneous HIV-M.tb infections during iron loading and the feasibility of evaluating this in vitro.

摘要

铁螯合剂作为治疗铁过载病症的药物,对艾滋病和结核病(TB)有影响,因为体内过量的铁会促进艾滋病毒和结核分枝杆菌(M.tb)的繁殖。过量的铁,尤其是由于饮食习惯导致的,在撒哈拉以南非洲几乎与这两种病原体的感染一样普遍。艾滋病毒和结核分枝杆菌在共同感染期间相互影响彼此的复制,这一点已得到充分证实,但在铁过载条件下对两者同时感染进行体外评估以及确定螯合剂是否能逆转这种影响的研究有限。本综述简要评论了目前临床使用的铁螯合剂在铁负荷期间影响艾滋病毒与结核分枝杆菌同时感染的可能性以及在体外进行评估的可行性。

相似文献

1
Iron chelation as therapy for HIV and Mycobacterium tuberculosis co-infection under conditions of iron overload.在铁过载情况下,铁螯合作为治疗HIV与结核分枝杆菌合并感染的方法。
Curr Pharm Des. 2006;12(16):1943-7. doi: 10.2174/138161206777442164.
2
The effect of the host's iron status on tuberculosis.宿主铁状态对结核病的影响。
J Infect Dis. 2007 Jun 15;195(12):1745-53. doi: 10.1086/518040. Epub 2007 May 4.
3
Necrosis of host cells and survival of pathogens following iron overload in an in vitro model of co-infection with human immunodeficiency virus (HIV) and Mycobacterium tuberculosis.在人类免疫缺陷病毒(HIV)与结核分枝杆菌共感染的体外模型中,铁过载后宿主细胞坏死及病原体存活情况。
Int J Antimicrob Agents. 2007 Apr;29(4):465-70. doi: 10.1016/j.ijantimicag.2006.11.009. Epub 2007 Jan 22.
4
Iron and Mycobacterium tuberculosis infection.铁与结核分枝杆菌感染
J Clin Virol. 2001 Feb;20(3):123-6. doi: 10.1016/s1386-6532(00)00136-0.
5
Iron overload and tuberculosis: a case for iron chelation therapy.铁过载与结核病:铁螯合疗法的一个实例
Int J Tuberc Lung Dis. 2005 Jan;9(1):2-9.
6
Iron and iron chelating agents modulate Mycobacterium tuberculosis growth and monocyte-macrophage viability and effector functions.铁及铁螯合剂可调节结核分枝杆菌的生长以及单核细胞 - 巨噬细胞的活力和效应功能。
FEMS Immunol Med Microbiol. 2005 Aug 1;45(2):103-12. doi: 10.1016/j.femsim.2005.02.007. Epub 2005 Mar 30.
7
Transfusional iron overload and iron chelation therapy in thalassemia major and sickle cell disease.重型地中海贫血和镰状细胞病中的输血性铁过载与铁螯合疗法。
Hematol Oncol Clin North Am. 2014 Aug;28(4):703-27, vi. doi: 10.1016/j.hoc.2014.04.004.
8
Treatment of Virulent Mycobacterium tuberculosis and HIV Coinfected Macrophages with Gallium Nanoparticles Inhibits Pathogen Growth and Modulates Macrophage Cytokine Production.用镓纳米粒子治疗毒力结核分枝杆菌和 HIV 共感染的巨噬细胞可抑制病原体生长并调节巨噬细胞细胞因子的产生。
mSphere. 2019 Jul 24;4(4):e00443-19. doi: 10.1128/mSphere.00443-19.
9
The role of iron and chelators on infections in iron overload and non iron loaded conditions: prospects for the design of new antimicrobial therapies.铁和螯合剂在铁过载及非铁负荷状态下对感染的作用:新型抗菌疗法设计的前景
Hemoglobin. 2010 Jun;34(3):227-39. doi: 10.3109/03630269.2010.483662.
10
Design of iron chelators with therapeutic application.具有治疗应用的铁螯合剂的设计。
Dalton Trans. 2012 Jun 7;41(21):6371-89. doi: 10.1039/c2dt12159j. Epub 2012 Mar 6.

引用本文的文献

1
Low iron mitigates viral survival: insights from evolution, genetics, and pandemics-a review of current hypothesis.低铁水平可减轻病毒存活:来自进化、遗传学和大流行的见解——当前假说综述
Egypt J Med Hum Genet. 2020;21(1):75. doi: 10.1186/s43042-020-00114-z. Epub 2020 Dec 16.
2
Therapeutic Potential of Iron Chelators in Viral Diseases: A Systematic Review.铁螯合剂在病毒病治疗中的潜力:系统评价。
Curr Med Chem. 2024;31(27):4383-4391. doi: 10.2174/0109298673259596231211113211.
3
Ferroptosis: A mixed blessing for infectious diseases.铁死亡:传染病的祸福相依
Front Pharmacol. 2022 Sep 7;13:992734. doi: 10.3389/fphar.2022.992734. eCollection 2022.
4
Host-Pathogen Interaction as a Novel Target for Host-Directed Therapies in Tuberculosis.宿主-病原体相互作用作为结核病宿主导向治疗的新靶点。
Front Immunol. 2020 Jul 21;11:1553. doi: 10.3389/fimmu.2020.01553. eCollection 2020.
5
Commentary: Could iron chelators prove to be useful as an adjunct to COVID-19 Treatment Regimens?述评:铁螯合剂作为 COVID-19 治疗方案的辅助手段是否有效?
Metabolism. 2020 Jul;108:154260. doi: 10.1016/j.metabol.2020.154260. Epub 2020 May 8.
6
Bacterial Resistance in Pneumonia in Developing Countries-A Role for Iron Chelation.发展中国家肺炎中的细菌耐药性——铁螯合的作用
Trop Med Infect Dis. 2019 Apr 10;4(2):59. doi: 10.3390/tropicalmed4020059.
7
A major role for ferroptosis in -induced cell death and tissue necrosis.铁死亡在细胞死亡和组织坏死中的主要作用。
J Exp Med. 2019 Mar 4;216(3):556-570. doi: 10.1084/jem.20181776. Epub 2019 Feb 20.
8
Iron at the Centre of Interactions.铁处于相互作用的中心。
Front Cell Infect Microbiol. 2018 Jun 5;8:185. doi: 10.3389/fcimb.2018.00185. eCollection 2018.
9
Heparin inhibits intracellular Mycobacterium tuberculosis bacterial replication by reducing iron levels in human macrophages.肝素通过降低人巨噬细胞中的铁水平来抑制细胞内结核分枝杆菌的复制。
Sci Rep. 2018 May 8;8(1):7296. doi: 10.1038/s41598-018-25480-y.
10
Deferoxamine compensates for decreases in B cell counts and reduces mortality in enterovirus 71-infected mice.去铁胺可弥补B细胞数量的减少,并降低肠道病毒71型感染小鼠的死亡率。
Mar Drugs. 2014 Jul 7;12(7):4086-95. doi: 10.3390/md12074086.