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重新利用异恶唑啉类兽用药物来控制媒介传播的人类疾病。

Repurposing isoxazoline veterinary drugs for control of vector-borne human diseases.

机构信息

TropIQ Health Sciences, 6534 Nijmegen, The Netherlands.

MRC Centre for Outbreak Analysis and Modelling, Department of Infectious Disease Epidemiology, Imperial College London, London SW7 2AZ, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2018 Jul 17;115(29):E6920-E6926. doi: 10.1073/pnas.1801338115. Epub 2018 Jul 2.

Abstract

Isoxazolines are oral insecticidal drugs currently licensed for ectoparasite control in companion animals. Here we propose their use in humans for the reduction of vector-borne disease incidence. Fluralaner and afoxolaner rapidly killed , , and mosquitoes and sand flies after feeding on a drug-supplemented blood meal, with IC values ranging from 33 to 575 nM, and were fully active against strains with preexisting resistance to common insecticides. Based on allometric scaling of preclinical pharmacokinetics data, we predict that a single human median dose of 260 mg (IQR, 177-407 mg) for afoxolaner, or 410 mg (IQR, 278-648 mg) for fluralaner, could provide an insecticidal effect lasting 50-90 days against mosquitoes and sand flies. Computational modeling showed that seasonal mass drug administration of such a single dose to a fraction of a regional population would dramatically reduce clinical cases of Zika and malaria in endemic settings. Isoxazolines therefore represent a promising new component of drug-based vector control.

摘要

异恶唑啉类药物是目前获准用于控制伴侣动物外寄生虫的口服杀虫药物。在这里,我们提议将其用于人类,以降低虫媒病的发病率。在摄入添加药物的血餐后,氟雷拉纳和阿福拉纳迅速杀死了 和 蚊子和 沙蝇,其 IC 值范围为 33 至 575 nM,并且对具有常见杀虫剂预先存在抗性的菌株完全有效。基于临床前药代动力学数据的比例缩放,我们预测单次人类中位数剂量为 260 毫克(IQR,177-407 毫克)的阿福拉纳,或 410 毫克(IQR,278-648 毫克)的氟雷拉纳,可对蚊子和沙蝇产生长达 50-90 天的杀虫效果。计算模型表明,在流行地区,对部分人群进行季节性大规模药物给药,将显著减少地方性流行地区的寨卡和疟疾临床病例。因此,异恶唑啉类药物代表了一种有前途的新型药物控制媒介的新成分。

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