Drug-resistant malaria: Molecular mechanisms and implications for public health

被引:184
作者
Petersen, Ines [1 ]
Eastman, Richard [2 ]
Lanzer, Michael [1 ]
机构
[1] Univ Klinikum Heidelberg, Dept Infect Dis, D-69120 Heidelberg, Germany
[2] NIAID, Malaria Funct Genom Sect, Lab Malaria & Vector Res, DIR,NIH, Rockville, MD 20852 USA
关键词
Drug resistance; Antimalarial drug; pfcrt; pfmdr1; Plasmodium falciparum; Plasmodium vivax; PLASMODIUM-FALCIPARUM MALARIA; IN-VITRO SUSCEPTIBILITY; P-GLYCOPROTEIN HOMOLOG; TRANSMEMBRANE PROTEIN PFCRT; EXCHANGER PFNHE-1 GENE; CHLOROQUINE RESISTANCE; ANTIMALARIAL-DRUG; NA+/H+ EXCHANGER; DIHYDROFOLATE-REDUCTASE; ARTEMETHER-LUMEFANTRINE;
D O I
10.1016/j.febslet.2011.04.042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Resistance to antimalarial drugs has often threatened malaria elimination efforts and historically has led to the short-term resurgence of malaria incidences and deaths. With concentrated malaria eradication efforts currently underway, monitoring drug resistance in clinical settings complemented by in vitro drug susceptibility assays and analysis of resistance markers, becomes critical to the implementation of an effective antimalarial drug policy. Understanding of the factors, which lead to the development and spread of drug resistance, is necessary to design optimal prevention and treatment strategies. This review attempts to summarize the unique factors presented by malarial parasites that lead to the emergence and spread of drug resistance, and gives an overview of known resistance mechanisms to currently used antimalarial drugs. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1551 / 1562
页数:12
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