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Effect of antimalarial drugs on Plasmodium falciparum gametocytes.抗疟药物对恶性疟原虫配子体的作用。
J Infect Dis. 2009 Nov 15;200(10):1518-21. doi: 10.1086/644645.
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From malaria control to eradication: The WHO perspective.从疟疾控制到消除:世界卫生组织的观点。
Trop Med Int Health. 2009 Jul;14(7):802-9. doi: 10.1111/j.1365-3156.2009.02287.x. Epub 2009 May 26.
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A green fluorescent protein-based assay for determining gametocyte production in Plasmodium falciparum.一种基于绿色荧光蛋白的用于测定恶性疟原虫配子体产生的检测方法。
Mol Biochem Parasitol. 2009 Feb;163(2):123-6. doi: 10.1016/j.molbiopara.2008.10.004. Epub 2008 Nov 5.
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New treatment options for HIV salvage patients: an overview of second generation PIs, NNRTIs, integrase inhibitors and CCR5 antagonists.HIV挽救治疗患者的新治疗选择:第二代蛋白酶抑制剂、非核苷类逆转录酶抑制剂、整合酶抑制剂及CCR5拮抗剂概述
J Infect. 2008 Jul;57(1):1-10. doi: 10.1016/j.jinf.2008.05.006. Epub 2008 Jun 16.
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HIV and malaria co-infection: interactions and consequences of chemotherapy.艾滋病毒与疟疾合并感染:化疗的相互作用及后果
Trends Parasitol. 2008 Jun;24(6):264-71. doi: 10.1016/j.pt.2008.03.008. Epub 2008 May 2.
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Influence of oxygen on asexual blood cycle and susceptibility of Plasmodium falciparum to chloroquine: requirement of a standardized in vitro assay.氧气对恶性疟原虫无性血液周期及对氯喹敏感性的影响:标准化体外测定法的必要性
Malar J. 2007 Apr 16;6:44. doi: 10.1186/1475-2875-6-44.
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Antimalarial activity of sera from subjects taking HIV protease inhibitors.服用HIV蛋白酶抑制剂的受试者血清的抗疟活性。
AIDS. 2007 Mar 30;21(6):763-5. doi: 10.1097/QAD.0b013e328031f41a.
8
Synergistic interactions of the antiretroviral protease inhibitors saquinavir and ritonavir with chloroquine and mefloquine against Plasmodium falciparum in vitro.抗逆转录病毒蛋白酶抑制剂沙奎那韦和利托那韦与氯喹和甲氟喹在体外对恶性疟原虫的协同相互作用。
Antimicrob Agents Chemother. 2007 Feb;51(2):759-62. doi: 10.1128/AAC.00840-06. Epub 2006 Nov 6.
9
Tipranavir: a novel nonpeptidic protease inhibitor of HIV.替拉那韦:一种新型的HIV非肽类蛋白酶抑制剂。
Clin Pharmacokinet. 2006;45(7):665-82. doi: 10.2165/00003088-200645070-00003.
10
Increased severe anemia in HIV-1-exposed and HIV-1-positive infants and children during acute malaria.在急性疟疾期间,暴露于HIV-1和HIV-1阳性的婴幼儿严重贫血情况增加。
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抗疟无性生殖阶段特异性和配子体杀伤活性的 HIV 蛋白酶抑制剂。

Antimalarial asexual stage-specific and gametocytocidal activities of HIV protease inhibitors.

机构信息

Queensland Institute of Medical Research, 300 Herston Rd., Herston, Queensland, Australia.

出版信息

Antimicrob Agents Chemother. 2010 Mar;54(3):1334-7. doi: 10.1128/AAC.01512-09. Epub 2009 Dec 22.

DOI:10.1128/AAC.01512-09
PMID:20028821
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825985/
Abstract

The stage-specific antimalarial activities of a panel of antiretroviral protease inhibitors (PIs), including two nonpeptidic PIs (tipranavir and darunavir), were tested in vitro against Plasmodium falciparum. While darunavir demonstrated limited antimalarial activity (effective concentration [EC(50)], >50 microM), tipranavir was active at clinically relevant concentrations (EC(50), 12 to 21 microM). Saquinavir, lopinavir, and tipranavir preferentially inhibited the growth of mature asexual-stage parasites (24 h postinvasion). While all of the PIs tested inhibited gametocytogenesis, tipranavir was the only one to exhibit gametocytocidal activity.

摘要

研究人员检测了一组抗逆转录病毒蛋白酶抑制剂(PI),包括两种非肽类 PI(替拉那韦和达芦那韦)的抗疟活性,这些药物针对恶性疟原虫(Plasmodium falciparum)在体外的不同阶段进行了测试。达芦那韦显示出有限的抗疟活性(有效浓度[EC(50)],大于 50 微摩尔),而替拉那韦在临床相关浓度下具有活性(EC(50),12 至 21 微摩尔)。沙奎那韦、洛匹那韦和替拉那韦优先抑制成熟的无性期寄生虫的生长(入侵后 24 小时)。虽然所有测试的 PI 都抑制配子体形成,但只有替拉那韦表现出配子体杀伤活性。