Wisniewski Thomas, Boutajangout Allal
Department of Neurology, New York University School of Medicine, New York, NY, USA.
Mt Sinai J Med. 2010 Jan-Feb;77(1):17-31. doi: 10.1002/msj.20156.
Alzheimer's disease is the most common cause of dementia worldwide. Alzheimer's disease is a member of a broad range of neurodegenerative diseases characterized pathologically by the conformational change of a normal protein into a pathological conformer with a high beta-sheet content that renders it neurotoxic. In the case of Alzheimer's disease, the normal soluble amyloid beta peptide is converted into oligomeric/fibrillar amyloid beta. The oligomeric forms of amyloid beta have been hypothesized to be the most toxic, whereas fibrillar amyloid beta becomes deposited as amyloid plaques and congophilic angiopathy, which both serve as neuropathological markers of the disease. In addition, the accumulation of abnormally phosphorylated tau as soluble toxic oligomers and as neurofibrillary tangles is a critical part of the pathology. Numerous therapeutic interventions are under investigation to prevent and treat Alzheimer's disease. Among the most exciting and advanced of these approaches is vaccination. Immunomodulation is being tried for a range of neurodegenerative disorders, with great success being reported in most model animal trials; however, the much more limited human data have shown more modest clinical success so far, with encephalitis occurring in a minority of patients treated with active immunization. The immunomodulatory approaches for neurodegenerative diseases involve targeting a self-protein, albeit in an abnormal conformation; hence, effective enhanced clearance of the disease-associated conformer has to be balanced with the potential risk of stimulating excessive toxic inflammation within the central nervous system. The design of future immunomodulatory approaches that are more focused is dependent on addressing a number of questions, including when is the best time to start immunization, what are the most appropriate targets for vaccination, and is amyloid central to the pathogenesis of Alzheimer's disease or is it critical to target tau-related pathology also. In this review, we discuss the past experience with vaccination for Alzheimer's disease and the development of possible future strategies that target both amyloid beta-related and tau-related pathologies.
阿尔茨海默病是全球痴呆最常见的病因。阿尔茨海默病是一系列神经退行性疾病的一种,其病理特征是正常蛋白质发生构象变化,转变为具有高β-折叠含量的病理构象体,从而具有神经毒性。就阿尔茨海默病而言,正常的可溶性淀粉样β肽会转变为寡聚体/纤维状淀粉样β。淀粉样β的寡聚体形式被认为毒性最强,而纤维状淀粉样β会沉积为淀粉样斑块和嗜刚果红血管病变,二者均为该疾病的神经病理学标志物。此外,异常磷酸化的tau蛋白以可溶性毒性寡聚体和神经原纤维缠结的形式积累是病理过程的关键部分。目前正在研究多种治疗干预措施来预防和治疗阿尔茨海默病。其中最令人兴奋且进展最为先进的方法之一是疫苗接种。免疫调节正在用于一系列神经退行性疾病的治疗,在大多数模型动物试验中都取得了巨大成功;然而,目前人类数据更为有限,迄今为止临床成功较为有限,少数接受主动免疫治疗的患者出现了脑炎。神经退行性疾病的免疫调节方法涉及针对一种自身蛋白,尽管其构象异常;因此,有效增强清除与疾病相关的构象体必须与刺激中枢神经系统内过度毒性炎症的潜在风险相平衡。未来更具针对性的免疫调节方法的设计取决于解决一系列问题,包括何时开始免疫接种最佳、疫苗接种的最合适靶点是什么,以及淀粉样蛋白是否是阿尔茨海默病发病机制的核心,或者靶向与tau相关的病理是否也至关重要。在本综述中,我们讨论了阿尔茨海默病疫苗接种的过往经验以及未来可能针对淀粉样β相关和tau相关病理的策略发展。