Drugs and drug resistance in African trypanosomiasis

被引:209
作者
Delespaux, Vincent
de Koning, Harry P.
机构
[1] Univ Glasgow, Inst Biomed & Life Sci, Div Infect & Immun, Glasgow G12 8QQ, Lanark, Scotland
[2] Inst Trop Med, Dept Anim Hlth, Trypanosomosis Unit, B-2000 Antwerp, Belgium
关键词
sleeping sickness; trypanosomiasis; Trypanosoma brucei; chemotherapy; drug resistance; pentamidine; melarsoprol; nifurtimox;
D O I
10.1016/j.drup.2007.02.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the many decades of use of most of the current trypanocides, we know little of their mode of action. This may in part be because most of these will act on multiple targets once inside the cell, and they derive their selective action on the parasite from selective accumulation by the pathogen. Loss of this capacity for drug uptake by the trypanosome would thus be a major cause for drug resistance. We here discuss the use of current drugs against human and veterinary African trypanosomiasis, the prevalence, causes and mechanisms of drug resistance and new developments in trypanosomiasis therapy such as the introduction of nifurtimox and DB289. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 50
页数:21
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