Department of Neuroscience and Physiology, New York University Grossman School of Medicine, New York, NY, USA.
Neuroscience Institute, New York University Grossman School of Medicine, New York, NY, USA.
Nat Rev Neurol. 2023 Dec;19(12):715-736. doi: 10.1038/s41582-023-00883-2. Epub 2023 Oct 24.
Alzheimer disease (AD) is the most common cause of dementia in older individuals. AD is characterized pathologically by amyloid-β (Aβ) plaques and tau neurofibrillary tangles in the brain, with associated loss of synapses and neurons, which eventually results in dementia. Many of the early attempts to develop treatments for AD focused on Aβ, but a lack of efficacy of these treatments in terms of slowing disease progression led to a change of strategy towards targeting of tau pathology. Given that tau shows a stronger correlation with symptom severity than does Aβ, targeting of tau is more likely to be efficacious once cognitive decline begins. Anti-tau therapies initially focused on post-translational modifications, inhibition of tau aggregation and stabilization of microtubules. However, trials of many potential drugs were discontinued because of toxicity and/or lack of efficacy. Currently, the majority of tau-targeting agents in clinical trials are immunotherapies. In this Review, we provide an update on the results from the initial immunotherapy trials and an overview of new therapeutic candidates that are in clinical development, as well as considering future directions for tau-targeting therapies.
阿尔茨海默病(AD)是老年人中最常见的痴呆症病因。AD 在病理学上的特征是大脑中存在淀粉样蛋白-β(Aβ)斑块和 tau 神经原纤维缠结,伴随着突触和神经元的丧失,最终导致痴呆。许多早期开发 AD 治疗方法的尝试都集中在 Aβ 上,但这些治疗方法在减缓疾病进展方面缺乏疗效,这导致了策略的改变,转向针对 tau 病理学。鉴于 tau 与症状严重程度的相关性强于 Aβ,一旦认知能力下降开始,针对 tau 的治疗就更有可能有效。针对 tau 的治疗方法最初集中在翻译后修饰、抑制 tau 聚集和稳定微管上。然而,由于毒性和/或疗效不佳,许多潜在药物的试验都已停止。目前,临床试验中大多数针对 tau 的药物都是免疫疗法。在这篇综述中,我们提供了初始免疫疗法试验的最新结果,并概述了正在临床开发的新治疗候选物,同时还考虑了针对 tau 的治疗方法的未来方向。