Kennedy Peter G E
Department of Neurology, Division of Clinical Neurosciences, University of Glasgow, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK.
Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1061-2. doi: 10.1016/j.trstmh.2007.05.001. Epub 2007 Jun 4.
Animal models of human African trypanosomiasis, also known as sleeping sickness, have been used for many years both to investigate disease pathogenesis and to test novel drug therapies. Model systems used have included mice, rats and non-human primates such as monkeys. Whilst such animal models have some definite but unavoidable limitations, it is argued that these are outweighed by their advantages. The latter include the ability to investigate disease pathogenesis mechanistically and the mechanisms of trypanosome traversal of the blood-brain barrier, as well as the identification of new potential drug targets and staging biomarkers, new drug therapies and combinations, and potential drug toxicity.
人类非洲锥虫病(又称昏睡病)的动物模型已经使用多年,用于研究疾病发病机制和测试新型药物疗法。所使用的模型系统包括小鼠、大鼠和非人类灵长类动物,如猴子。虽然这些动物模型有一些明确但不可避免的局限性,但有人认为其优势超过了这些局限性。优势包括能够从机制上研究疾病发病机制以及锥虫穿越血脑屏障的机制,还包括识别新的潜在药物靶点和分期生物标志物、新的药物疗法和联合用药,以及潜在的药物毒性。