Eck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA; Warren Family Center for Drug Discovery and Development, University of Notre Dame, Notre Dame, IN, USA.
Eck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Int J Antimicrob Agents. 2019 Oct;54(4):496-501. doi: 10.1016/j.ijantimicag.2019.07.013. Epub 2019 Jul 16.
Leishmania parasites are the causative agents of a wide spectrum of human diseases. The clinical manifestations of leishmaniasis range from self-healing skin lesions to fatality. The World Health Organization has classed leishmaniasis as a category 1 neglected tropical disease. Leishmaniasis represents a major international health challenge, affecting 12 million people per year and with nearly 310 million people at risk. The first-line chemotherapies used to treat leishmaniasis are intravenous pentavalent antimonials; however, these drugs are highly toxic. As the use of oral treatment options such as paromomycin and miltefosine has increased, the incidence of disease relapse has increased and drug resistance to antimonials has developed, emphasizing the importance of identifying new chemotherapies. A novel, target-free fluorometric high-throughput screen with an average Z-score of 0.73 +/- 0.13 has been developed to identify small molecules with antileishmanial activity. Screening of 10,000 small molecules from the ChemBridge DIVER-set™ library cassette #5 yielded 210 compounds that killed 80% of parasites, resulting in a hit rate of 2.1%. One hundred and nine molecular scaffolds were represented within the hit compounds, and one scaffold that exhibited potent antileishmanial activity was 2,4-diaminoquinazoline. Host cell toxicity was determined prior to in-vitro infection of human THP-1 macrophages with Leishmania donovani mCherry expressing promastigotes; successful drug treatment was considered when the half maximal inhibitory concentration was <10 µM. BALB/c mice were infected with Leishmania major mCherry promastigotes and treated with small molecules that were successful during in-vitro infections. Several small molecules tested were as efficacious at resolving cutaneous leishmaniasis lesions in mice as known antimonial treatments.
利什曼原虫寄生虫是广泛的人类疾病的病原体。利什曼病的临床表现从自我修复的皮肤损伤到致命不等。世界卫生组织已将利什曼病归类为 1 类被忽视的热带病。利什曼病代表了一个主要的国际健康挑战,每年影响 1200 万人,有近 3.1 亿人面临风险。用于治疗利什曼病的一线化疗药物是静脉注射五价锑;然而,这些药物毒性很高。随着诸如巴龙霉素和米替福新等口服治疗选择的使用增加,疾病复发的发生率增加,并且对锑的耐药性也有所发展,这强调了确定新化疗药物的重要性。已经开发出一种新颖的、无靶标荧光高通量筛选方法,平均 Z 分数为 0.73 +/- 0.13,用于鉴定具有抗利什曼原虫活性的小分子。从 ChemBridge DIVER-set™库盒 #5 筛选了 10,000 种小分子,发现有 210 种化合物能杀死 80%的寄生虫,因此命中率为 2.1%。在人类 THP-1 巨噬细胞与表达前鞭毛体的利什曼原虫 donovani mCherry 体外感染之前,测定了宿主细胞毒性;当半最大抑制浓度 <10 µM 时,认为药物治疗成功。用利什曼原虫 major mCherry 前鞭毛体感染 BALB/c 小鼠,并对在体外感染中成功的小分子进行治疗。在小鼠中测试的几种小分子在解决皮肤利什曼病病变方面与已知的锑治疗一样有效。