Fügi Matthias A, Kaiser Marcel, Tanner Marcel, Schneiter Roger, Mäser Pascal, Guan Xue Li
Swiss Tropical and Public Health Institute, CH-4051 Basel, Switzerland; University of Basel, CH-4000 Basel, Switzerland.
University of Fribourg, CH-1700 Fribourg, Switzerland.
Trends Parasitol. 2015 Feb;31(2):46-51. doi: 10.1016/j.pt.2014.11.004. Epub 2014 Dec 6.
Currently available drugs for Chagas' disease are limited by toxicity and low efficacy in the chronic stage. Posaconazole, the most advanced new anti-chagasic drug candidate, did not fully confirm its initial potential in a Phase II clinical trial for chronic Chagas' disease. Given that posaconazole is highly active against Trypanosoma cruzi in vitro, and was very well tolerated in clinical trials, it should not be abandoned. Rather, a combination therapy may provide a highly promising outlook. Systems-scale approaches facilitate the hunt for a combination partner for posaconazole, which acts by blocking sterol biosynthesis. Mounting evidence suggests the functional interactions between sterols and sphingolipids in vivo. Here, we propose combining sterol and sphingolipid biosynthesis inhibitors to advance drug development in Chagas' disease.
目前可用于治疗恰加斯病的药物受到毒性限制,且在慢性阶段疗效较低。泊沙康唑是最先进的新型抗恰加斯病候选药物,在慢性恰加斯病的II期临床试验中未完全证实其最初的潜力。鉴于泊沙康唑在体外对克氏锥虫具有高度活性,且在临床试验中耐受性良好,不应将其放弃。相反,联合疗法可能会带来非常有前景的前景。系统规模的方法有助于寻找泊沙康唑的联合用药伙伴,泊沙康唑通过阻断甾醇生物合成发挥作用。越来越多的证据表明体内甾醇和鞘脂之间存在功能相互作用。在此,我们建议联合使用甾醇和鞘脂生物合成抑制剂来推进恰加斯病的药物开发。