Recent developments in tau-based therapeutics for neurodegenerative diseases.

Miguel Medina
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引用次数: 29

Abstract

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.

以tau蛋白为基础的神经退行性疾病治疗的最新进展。
由于医疗保健的普遍改善和人口结构的变化,人口老龄化日益严重,神经退行性疾病构成了一个重大的公共卫生问题。目前使用胆碱酯酶抑制剂或NMDA拮抗剂治疗阿尔茨海默病(AD)(最常见的痴呆症)的药物已显示出非常温和的症状性疗效,因此对新的、更有效的治疗方法的医学需求尚未得到满足。在过去的二十年里,阿尔茨海默病的药物开发工作主要集中在淀粉样蛋白级联假说定义的靶点上,到目前为止,结果令人失望。相比之下,尽管广泛的tau病理是该疾病的核心,但直到最近,基于tau的策略才受到很少的关注。导致额颞叶痴呆的tau基因突变的发现表明,在没有淀粉样蛋白病理的情况下,tau功能障碍足以导致神经元丢失和临床痴呆。本文综述了旨在治疗tau病变和AD中tau病理的潜在原因的新兴治疗策略,包括一些在该领域具有重大潜力的靶点,这些靶点可能在未来几年内提供新的治疗范例。在这些策略中,将主要讨论免疫治疗方法。还提供了关于基于tau的治疗策略的不同方面的2010年专利的最新情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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