Barrett M P, Boykin D W, Brun R, Tidwell R R
Division of Infection and Immunity, Institute of Biomedical and Life Sciences, The Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, UK.
Br J Pharmacol. 2007 Dec;152(8):1155-71. doi: 10.1038/sj.bjp.0707354. Epub 2007 Jul 9.
This review discusses the challenges of chemotherapy for human African trypanosomiasis (HAT). The few drugs registered for use against the disease are unsatisfactory for a number of reasons. HAT has two stages. In stage 1 the parasites proliferate in the haemolymphatic system. In stage 2 they invade the central nervous system and brain provoking progressive neurological dysfunction leading to symptoms that include the disrupted sleep wake patterns that give HAT its more common name of sleeping sickness. Targeting drugs to the central nervous system offers many challenges. However, it is the cost of drug development for diseases like HAT, that afflict exclusively people of the world's poorest populations, that has been the principal barrier to new drug development and has led to them becoming neglected. Here we review drugs currently registered for HAT, and also discuss the few compounds progressing through clinical trials. Finally we report on new initiatives that might allow progress to be made in developing new and satisfactory drugs for this terrible disease.
本综述探讨了治疗人类非洲锥虫病(HAT)的化疗挑战。由于多种原因,目前登记用于治疗该疾病的药物寥寥无几,且效果不尽人意。HAT有两个阶段。在第一阶段,寄生虫在血淋巴系统中增殖。在第二阶段,它们侵入中枢神经系统和大脑,引发进行性神经功能障碍,导致包括睡眠-觉醒模式紊乱等症状,这也是HAT更常用的名称昏睡病的由来。将药物靶向中枢神经系统存在诸多挑战。然而,像HAT这类仅折磨世界最贫困人群的疾病,药物研发成本才是新药研发的主要障碍,导致它们被忽视。在此,我们综述目前登记用于HAT的药物,也讨论少数正在进行临床试验的化合物。最后,我们报告一些新举措,这些举措可能会推动针对这种可怕疾病研发新的、令人满意的药物取得进展。