Medina Miguel
Noscira S.A.; Avenida de la Industria, 52; 28760 Tres Cantos (Madrid), Spain.
Recent Pat CNS Drug Discov. 2011 Jan;6(1):20-30. doi: 10.2174/157488911794079091.
Neurodegenerative diseases constitute a major public health issue due to an increasingly aged population as a consequence of generally improved medical care and demographic changes. Current drug treatment of Alzheimer's disease (AD), the most prevalent dementia, with cholinesterase inhibitors or NMDA antagonists has demonstrated very modest, symptomatic efficacy, leaving an unmet medical need for new, more effective therapies. Drug development efforts for AD in the last two decades have primarily focused on targets defined by the amyloid cascade hypothesis, so far with disappointing results. In contrast, tau-based strategies have received little attention until recently despite that the presence of extensive tau pathology is central to the disease. The discovery of mutations within the tau gene that cause fronto-temporal dementia demonstrated that tau dysfunction, in the absence of amyloid pathology, was sufficient to cause neuronal loss and clinical dementia. This review focuses on emerging therapeutic strategies aimed at treating the underlying causes of the tau pathology in tauopathies and AD, including some targets with significant potential in the field and which might be on the verge of providing new treatment paradigms within the coming years. Among those strategies, immunotherapy approaches will be mostly discussed. An update on 2010 patents regarding different aspects of tau-based therapeutic strategies is also provided.
由于医疗条件普遍改善和人口结构变化导致人口老龄化加剧,神经退行性疾病已成为一个重大的公共卫生问题。目前,针对最常见的痴呆症——阿尔茨海默病(AD),使用胆碱酯酶抑制剂或NMDA拮抗剂进行药物治疗,疗效甚微且仅为对症治疗,对新型、更有效疗法的医疗需求仍未得到满足。在过去二十年中,AD的药物研发主要集中在淀粉样蛋白级联假说所定义的靶点上,然而迄今为止结果令人失望。相比之下,基于tau蛋白的策略直到最近才受到较少关注,尽管广泛存在的tau蛋白病变是该疾病的核心。tau基因内导致额颞叶痴呆的突变的发现表明,在没有淀粉样蛋白病变的情况下,tau蛋白功能障碍足以导致神经元丧失和临床痴呆。本综述重点关注旨在治疗tau蛋白病和AD中tau蛋白病变根本原因的新兴治疗策略,包括该领域具有重大潜力且可能在未来几年内带来新治疗模式的一些靶点。在这些策略中,将主要讨论免疫治疗方法。此外,还提供了2010年关于基于tau蛋白治疗策略不同方面的专利更新情况。