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抗疟药物耐药性的成本与效益

Costs and benefits of resistance against antimalarial drugs.

作者信息

Koella J C

机构信息

Department of Zoology, University of Aarhus, Universitetsparken B135, DK-8000 Aarhus, Denmark.

出版信息

Parasitol Today. 1998 Sep;14(9):360-4. doi: 10.1016/s0169-4758(98)01297-6.

DOI:10.1016/s0169-4758(98)01297-6
PMID:17040817
Abstract

Recent experiments have suggested that resistance to antimalarial drugs, in particular chloroquine, is associated with increased transmission. However, epidemiological patterns suggest the opposite: ie. that resistance should be associated with a transmission cost. Here, Jacob Koella reviews the evidence for either a cost or a benefit of chloroquine resistance and proposes ideas from population and evolutionary biology that might explain the apparent contradiction between experimental and epidemiological evidence.

摘要

近期的实验表明,对抗疟药物尤其是氯喹的耐药性与传播增加有关。然而,流行病学模式却显示出相反的情况:即耐药性应与传播成本相关。在此,雅各布·凯拉回顾了关于氯喹耐药性的成本或益处的证据,并提出了群体生物学和进化生物学的观点,这些观点或许可以解释实验证据与流行病学证据之间明显的矛盾。

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Costs and benefits of resistance against antimalarial drugs.抗疟药物耐药性的成本与效益
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2
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[Mechanisms and dynamics of drug resistance in Plasmodium falciparum].恶性疟原虫耐药性的机制与动态变化
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Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of antimalarial drug resistance.抗原株多样性预测了抗疟药物耐药性维持和下降的不同生物地理模式。
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Antigenic strain diversity predicts different biogeographic patterns of maintenance and decline of anti-malarial drug resistance.抗原菌株多样性预示着抗疟药物抗性维持和衰退的不同生物地理模式。
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Mathematical models of malaria--a review.
疟疾的数学模型——综述。
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Return of chloroquine-susceptible falciparum malaria in Malawi was a reexpansion of diverse susceptible parasites.马拉维对氯喹敏感的恶性疟原虫的卷土重来是多种敏感寄生虫的重新扩张。
J Infect Dis. 2010 Sep 1;202(5):801-8. doi: 10.1086/655659.
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The evolution of drug-resistant malaria: the role of drug elimination half-life.耐药疟疾的演变:药物消除半衰期的作用。
Philos Trans R Soc Lond B Biol Sci. 2002 Apr 29;357(1420):505-19. doi: 10.1098/rstb.2001.1036.
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Current status of malaria and potential for control.疟疾的现状与控制潜力
Clin Microbiol Rev. 2001 Jan;14(1):208-26. doi: 10.1128/CMR.14.1.208-226.2001.
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