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奥芬达唑对体内丝状线虫秀丽隐杆线虫具有杀微丝蚴作用,并抑制体外盘尾丝虫属运动。

Oxfendazole mediates macrofilaricidal efficacy against the filarial nematode Litomosoides sigmodontis in vivo and inhibits Onchocerca spec. motility in vitro.

机构信息

Institute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.

Unité Molécules de Communication et Adaptation des Microorganismes (MCAM, UMR 7245), Sorbonne Universités, Muséum national d'Histoire naturelle, CNRS, Paris, France.

出版信息

PLoS Negl Trop Dis. 2020 Jul 6;14(7):e0008427. doi: 10.1371/journal.pntd.0008427. eCollection 2020 Jul.

Abstract

A major impediment to eliminate lymphatic filariasis and onchocerciasis is the lack of effective short-course macrofilaricidal drugs or regimens that are proven to be safe for both infections. In this study we tested oxfendazole, an anthelmintic shown to be well tolerated in phase 1 clinical trials. In vitro, oxfendazole exhibited modest to marginal motility inhibition of adult worms of Onchocerca gutturosa, pre-adult worms of Onchocerca volvulus and Onchocerca lienalis microfilariae. In vivo, five days of oral treatments provided sterile cure with up to 100% macrofilaricidal efficacy in the murine Litomosoides sigmodontis model of filariasis. In addition, 10 days of oral treatments with oxfendazole inhibited filarial embryogenesis in patent L. sigmodontis-infected jirds and subsequently led to a protracted but complete clearance of microfilaremia. The macrofilaricidal effect observed in vivo was selective, as treatment with oxfendazole of microfilariae-injected naïve mice was ineffective. Based on pharmacokinetic analysis, the driver of efficacy is the maintenance of a minimal efficacious concentration of approximately 100 ng/ml (based on subcutaneous treatment at 25 mg/kg in mice). From animal models, the human efficacious dose is predicted to range from 1.5 to 4.1 mg/kg. Such a dose has already been proven to be safe in phase 1 clinical trials. Oxfendazole therefore has potential to be efficacious for treatment of human filariasis without causing adverse reactions due to drug-induced microfilariae killing.

摘要

消除淋巴丝虫病和盘尾丝虫病的一个主要障碍是缺乏有效的短期杀微丝蚴药物或方案,这些药物或方案已被证明对这两种感染都是安全的。在这项研究中,我们测试了奥芬达唑,一种在 1 期临床试验中被证明具有良好耐受性的驱虫药。在体外,奥芬达唑对盘尾丝虫的成虫、旋盘尾丝虫的未成熟成虫和奥氏曼森线虫的微丝蚴表现出适度至边缘的运动抑制作用。在体内,口服治疗 5 天可在利什曼原虫感染的小鼠淋巴丝虫病模型中提供无菌治愈,高达 100%的杀微丝蚴疗效。此外,口服奥芬达唑 10 天可抑制已感染的利什曼原虫感染沙鼠的丝虫胚胎发生,随后导致微丝蚴血症的持续但完全清除。体内观察到的杀微丝蚴作用是选择性的,因为用奥芬达唑治疗未感染微丝蚴的小鼠是无效的。基于药代动力学分析,疗效的驱动力是维持约 100ng/ml 的最小有效浓度(基于皮下治疗,在小鼠中 25mg/kg)。从动物模型来看,人类有效剂量预计在 1.5 至 4.1mg/kg 之间。这种剂量在 1 期临床试验中已被证明是安全的。因此,奥芬达唑有可能对治疗人类丝虫病有效,而不会因药物诱导的微丝蚴杀伤而引起不良反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7fe/7365463/3d9378ac7b8b/pntd.0008427.g001.jpg

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