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本文引用的文献

1
Artemisinin-induced parasite dormancy: a plausible mechanism for treatment failure.青蒿素诱导的寄生虫休眠:治疗失败的一种合理机制。
Malar J. 2011 Mar 8;10:56. doi: 10.1186/1475-2875-10-56.
2
Intrahost modeling of artemisinin resistance in Plasmodium falciparum.疟原虫青蒿素耐药性的宿主内建模。
Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):397-402. doi: 10.1073/pnas.1006113108. Epub 2010 Dec 20.
3
Artemisinin‐induced dormancy in plasmodium falciparum: duration, recovery rates, and implications in treatment failure.青蒿素诱导恶性疟原虫休眠:持续时间、恢复率及其对治疗失败的影响
J Infect Dis. 2010 Nov 1;202(9):1362-8. doi: 10.1086/656476.
4
Deamplification of pfmdr1-containing amplicon on chromosome 5 in Plasmodium falciparum is associated with reduced resistance to artelinic acid in vitro.恶性疟原虫 5 号染色体上 pfmdr1 基因扩增子的去扩增与体外对 artelinic acid 的耐药性降低有关。
Antimicrob Agents Chemother. 2010 Aug;54(8):3395-401. doi: 10.1128/AAC.01421-09. Epub 2010 Apr 26.
5
Exploring the contribution of candidate genes to artemisinin resistance in Plasmodium falciparum.探讨候选基因对恶性疟原虫青蒿素耐药性的贡献。
Antimicrob Agents Chemother. 2010 Jul;54(7):2886-92. doi: 10.1128/AAC.00032-10. Epub 2010 Apr 26.
6
Role of pfmdr1 amplification and expression in induction of resistance to artemisinin derivatives in Plasmodium falciparum.疟原虫 falciparum 中 pfmdr1 扩增和表达在诱导对青蒿素衍生物耐药中的作用。
Antimicrob Agents Chemother. 2010 Jun;54(6):2455-64. doi: 10.1128/AAC.00947-09. Epub 2010 Mar 29.
7
Increased tolerance to artemisinin in Plasmodium falciparum is mediated by a quiescence mechanism.疟原虫对青蒿素的耐受性增加是由休眠机制介导的。
Antimicrob Agents Chemother. 2010 May;54(5):1872-7. doi: 10.1128/AAC.01636-09. Epub 2010 Feb 16.
8
Artemisinin resistance in Plasmodium falciparum malaria.恶性疟原虫疟疾中的青蒿素耐药性。
N Engl J Med. 2009 Jul 30;361(5):455-67. doi: 10.1056/NEJMoa0808859.
9
Evidence of artemisinin-resistant malaria in western Cambodia.柬埔寨西部出现青蒿素耐药性疟疾的证据。
N Engl J Med. 2008 Dec 11;359(24):2619-20. doi: 10.1056/NEJMc0805011. Epub 2008 Dec 8.
10
Qinghaosu (artemisinin): the price of success.青蒿素:成功的代价
Science. 2008 Apr 18;320(5874):330-4. doi: 10.1126/science.1155165.

青蒿素耐药恶性疟原虫系的表型变化:对休眠和生长抑制敏感性降低的证据。

Phenotypic changes in artemisinin-resistant Plasmodium falciparum lines in vitro: evidence for decreased sensitivity to dormancy and growth inhibition.

机构信息

Drug Resistance and Diagnostics, Australian Army Malaria Institute, Brisbane, Australia.

出版信息

Antimicrob Agents Chemother. 2012 Jan;56(1):428-31. doi: 10.1128/AAC.05456-11. Epub 2011 Oct 10.

DOI:10.1128/AAC.05456-11
PMID:21986828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3256014/
Abstract

The appearance of Plasmodium falciparum parasites with decreased in vivo sensitivity but no measurable in vitro resistance to artemisinin has raised the urgent need to characterize the artemisinin resistance phenotype. Changes in the temporary growth arrest (dormancy) profile of parasites may be one aspect of this phenotype. In this study, we investigated the link between dormancy and resistance, using artelinic acid (AL)-resistant parasites. Our results demonstrate that the AL resistance phenotype has (i) decreased sensitivity of mature-stage parasites, (ii) decreased sensitivity of the ring stage to the induction of dormancy, and (iii) a faster recovery from dormancy.

摘要

疟原虫寄生虫外观出现对青蒿素的体内敏感性降低,但体外耐药性无法测量,这就迫切需要对青蒿素耐药表型进行特征描述。寄生虫的临时生长停滞(休眠)状态的变化可能是该表型的一个方面。在这项研究中,我们使用 artelinic 酸(AL)耐药寄生虫来研究休眠与耐药之间的联系。我们的研究结果表明,AL 耐药表型具有:(i)成熟阶段寄生虫的敏感性降低;(ii)环状阶段对休眠诱导的敏感性降低;以及(iii)从休眠中更快地恢复。