Jankowsky Joanna L, Savonenko Alena, Schilling Gabriele, Wang Jiou, Xu Guilian, Borchelt David R
Department of Pathology, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Ross Building Room 558, Baltimore, MD 21205, USA.
Curr Neurol Neurosci Rep. 2002 Sep;2(5):457-64. doi: 10.1007/s11910-002-0073-7.
Neurodegenerative diseases present an extraordinary challenge for medicine due to the grave nature of these illnesses, their prevalence, and their impact on individuals and caregivers. The most common of these age-associated chronic illnesses are Alzheimer's disease (AD) and Parkinson's disease (PD); other examples include the prion disorders, amyotrophic lateral sclerosis (ALS), and the trinucleotide (CAG) repeat diseases. All of these diseases are characterized by well-defined clinical syndromes with progressive courses that reflect the dysfunction and eventual loss of specific neuronal populations. Current therapies provide only symptomatic relief; none significantly alter the course of disease. We describe here how transgenic mice designed to model these diseases have substantially contributed to the identification and validation of many promising new therapies, and conversely how they have quickly and cost effectively eliminated several targets with unrealized expectations.
神经退行性疾病给医学带来了巨大挑战,这是由于这些疾病的严重性、患病率以及它们对患者和照料者的影响。这些与年龄相关的慢性疾病中最常见的是阿尔茨海默病(AD)和帕金森病(PD);其他例子包括朊病毒病、肌萎缩侧索硬化症(ALS)以及三核苷酸(CAG)重复疾病。所有这些疾病都具有明确的临床综合征,病程呈进行性,反映了特定神经元群体的功能障碍和最终丧失。目前的治疗仅提供症状缓解;没有一种能显著改变疾病进程。我们在此描述了旨在模拟这些疾病的转基因小鼠如何极大地促进了许多有前景的新疗法的识别和验证,反之,它们又如何迅速且经济高效地排除了几个期望未实现的靶点。