• 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

了解疟原虫的耐药性:公共卫生的基础科学。

Understanding drug resistance in malaria parasites: basic science for public health.

作者信息

Sibley Carol Hopkins

机构信息

World Wide Antimalarial Resistance Network, Department of Genome Sciences, University of Washington, Seattle, WA 98195-5065, USA.

出版信息

Mol Biochem Parasitol. 2014 Jul;195(2):107-14. doi: 10.1016/j.molbiopara.2014.06.001. Epub 2014 Jun 10.

DOI:10.1016/j.molbiopara.2014.06.001
PMID:24927641
Abstract

The worlds of basic scientists and those involved in treating patients and making public health decisions do not always intersect. Yet, assuring that when patients are treated, they are efficiently and completely cured, and that public health decisions are based on solid evidence requires a broad foundation of up to date basic research. Research on the malaria parasite, Plasmodium falciparum provides a useful illustration of the role that basic scientific studies have played in the very long relationship between humans and this deadly parasite. Drugs have always been a principal tool in malaria treatment. The ongoing struggle between evolution of resistance to antimalarials by the parasite and public health responses is used here as an illustration of the key contributions of basic scientists to this long history.

摘要

基础科学家的世界与那些参与治疗患者和做出公共卫生决策的人的世界并不总是相交的。然而,要确保患者在接受治疗时能够高效且完全治愈,并且公共卫生决策基于确凿的证据,就需要广泛的最新基础研究作为支撑。对疟原虫——恶性疟原虫的研究,很好地说明了基础科学研究在人类与这种致命寄生虫的长期关系中所发挥的作用。药物一直是疟疾治疗的主要工具。寄生虫对抗疟药物的耐药性演变与公共卫生应对措施之间持续不断的斗争,在此被用来说明基础科学家对这段悠久历史所做出的关键贡献。

相似文献

1
Understanding drug resistance in malaria parasites: basic science for public health.了解疟原虫的耐药性:公共卫生的基础科学。
Mol Biochem Parasitol. 2014 Jul;195(2):107-14. doi: 10.1016/j.molbiopara.2014.06.001. Epub 2014 Jun 10.
2
Antimalarial drug therapy: the role of parasite biology and drug resistance.抗疟药物治疗:寄生虫生物学与耐药性的作用
J Clin Pharmacol. 2006 Dec;46(12):1487-97. doi: 10.1177/0091270006294276.
3
Genetic and genomic approaches for the discovery of parasite genes involved in antimalarial drug resistance.用于发现与抗疟药物耐药性相关的寄生虫基因的遗传和基因组方法。
Parasitology. 2013 Oct;140(12):1455-67. doi: 10.1017/S0031182013000954. Epub 2013 Aug 9.
4
Spread and evolution of Plasmodium falciparum drug resistance.恶性疟原虫耐药性的传播与演变
Parasitol Int. 2009 Sep;58(3):201-9. doi: 10.1016/j.parint.2009.04.004. Epub 2009 Apr 23.
5
Helicases - feasible antimalarial drug target for Plasmodium falciparum.解旋酶——恶性疟原虫可行的抗疟药物靶点。
FEBS J. 2007 Sep;274(18):4699-704. doi: 10.1111/j.1742-4658.2007.06000.x.
6
The selection landscape of malaria parasites.疟原虫的选择景观。
Science. 2010 May 14;328(5980):866-71. doi: 10.1126/science.1185410.
7
The origins of antimalarial drug resistance.抗疟药物耐药性的起源。
Trends Parasitol. 2004 Nov;20(11):512-8. doi: 10.1016/j.pt.2004.08.006.
8
The biological and epidemiological basis of drug resistance in malaria parasites.疟原虫耐药性的生物学和流行病学基础。
Southeast Asian J Trop Med Public Health. 1992 Sep;23 Suppl 4:123-9.
9
An analytical presentation of drug resistance in Plasmodium falciparum and guidelines to formulate a drug strategy.恶性疟原虫耐药性的分析报告及制定药物策略的指南
J Commun Dis. 1995 Mar;27(1):44-54.
10
3,5-bis(benzylidene)-4-piperidones and related N-acyl analogs: a novel cluster of antimalarials targeting the liver stage of Plasmodium falciparum.3,5-双(亚苄基)-4-哌啶酮及相关的 N-酰基类似物:一组针对恶性疟原虫肝期的新型抗疟药物。
Bioorg Med Chem. 2013 Dec 1;21(23):7250-6. doi: 10.1016/j.bmc.2013.09.065. Epub 2013 Oct 8.

引用本文的文献

1
Evolutionary biology of antimalarial drug resistance: Understanding of the evolutionary dynamics.抗疟药物耐药性的进化生物学:对进化动力学的理解。
Medicine (Baltimore). 2025 Mar 14;104(11):e41878. doi: 10.1097/MD.0000000000041878.
2
Ex vivo Sensitivity Profile of Clinical Isolates to a Panel of Antimalarial Drugs in Ghana 13 Years After National Policy Change.加纳国家政策变更13年后临床分离株对一组抗疟药物的体外敏感性概况
Infect Drug Resist. 2021 Jan 28;14:267-276. doi: 10.2147/IDR.S295277. eCollection 2021.
3
The chromatin bound proteome of the human malaria parasite.
人类疟疾寄生虫的染色质结合蛋白质组。
Microb Genom. 2020 Feb;6(2). doi: 10.1099/mgen.0.000327. Epub 2020 Feb 4.
4
Uptake of a fluorescently tagged chloroquine analogue is reduced in CQ-resistant compared to CQ-sensitive Plasmodium falciparum parasites.与氯喹敏感型疟原虫相比,荧光标记的氯喹类似物在氯喹耐药型疟原虫中的摄取减少。
Malar J. 2019 Oct 7;18(1):342. doi: 10.1186/s12936-019-2980-y.
5
Proof of concept: used malaria rapid diagnostic tests applied for parallel sequencing for surveillance of molecular markers of anti-malarial resistance in Bissau, Guinea-Bissau during 2014-2017.概念验证:2014 年至 2017 年期间,在几内亚比绍比绍,使用疟疾快速诊断检测进行平行测序,以监测抗疟药物耐药性的分子标记。
Malar J. 2019 Jul 26;18(1):252. doi: 10.1186/s12936-019-2894-8.
6
Imported and autochthonous malaria in West Saudi Arabia: results from a reference hospital.沙特阿拉伯西部的输入性和本地疟疾:一家参考医院的结果。
Malar J. 2018 Aug 7;17(1):286. doi: 10.1186/s12936-018-2438-7.
7
Identifying host regulators and inhibitors of liver stage malaria infection using kinase activity profiles.利用激酶活性谱鉴定肝脏阶段疟原虫感染的宿主调控因子和抑制剂。
Nat Commun. 2017 Nov 1;8(1):1232. doi: 10.1038/s41467-017-01345-2.
8
Genetic Characterization of Plasmodium Putative Pantothenate Kinase Genes Reveals Their Essential Role in Malaria Parasite Transmission to the Mosquito.疟原虫假定泛酸激酶基因的遗传特征表明其在疟原虫向蚊子传播中的重要作用。
Sci Rep. 2016 Sep 20;6:33518. doi: 10.1038/srep33518.
9
Atovaquone and ELQ-300 Combination Therapy as a Novel Dual-Site Cytochrome bc1 Inhibition Strategy for Malaria.阿托伐醌与ELQ-300联合疗法作为一种新型的双位点细胞色素bc1抑制策略用于疟疾治疗。
Antimicrob Agents Chemother. 2016 Jul 22;60(8):4853-9. doi: 10.1128/AAC.00791-16. Print 2016 Aug.
10
A Method for Amplicon Deep Sequencing of Drug Resistance Genes in Plasmodium falciparum Clinical Isolates from India.一种用于对来自印度的恶性疟原虫临床分离株中耐药基因进行扩增子深度测序的方法。
J Clin Microbiol. 2016 Jun;54(6):1500-1511. doi: 10.1128/JCM.00235-16. Epub 2016 Mar 23.