Suppr超能文献

阿尔茨海默病:近期治疗策略

Alzheimer's disease: Recent treatment strategies.

作者信息

Vaz Miguel, Silvestre Samuel

机构信息

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, Covilhã, Portugal.

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, Covilhã, Portugal; CNC- Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.

出版信息

Eur J Pharmacol. 2020 Nov 15;887:173554. doi: 10.1016/j.ejphar.2020.173554. Epub 2020 Sep 15.

Abstract

Alzheimer Disease (AD) is a neurodegenerative disease characterized by two neuropathological hallmarks: extracellular deposition of amyloid plaques and intracellular neurofibrillary tangles. Current treatment for AD (donepezil, galantamine, rivastigmine and memantine) is only symptomatic and has modest benefits. Thus, the development of drugs with the potential to change the progression of the disease has been a priority. Therapies targeting amyloid β have been the focus for almost 30 years. However, highly promising drugs recently failed to show clinical benefits in phase III trials. Even the positive findings presented by Biogen on Aducanumab are not entirely clear and further data is necessary to confirm its validity. Therefore, researchers are turning their efforts around to tau-targeting therapies, since tau protein appears to be better correlated with the severity of cognitive decline than amyloid β. Currently, most anti-tau agents in clinical trials are immunotherapies and they are in the early stages of clinical research. Four monoclonal antibodies anti-tau (Gosuranemab, Tilavonemab, Semorinemab and Zagotenemab) and one anti-tau vaccine (AADvac1) have reached phase II, so far. In this review, we discuss the potential disease-modifying agents tested in clinical trials and update the information of drugs that are still under clinical evaluation.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,其具有两个神经病理学特征:细胞外淀粉样斑块沉积和细胞内神经原纤维缠结。目前针对AD的治疗药物(多奈哌齐、加兰他敏、卡巴拉汀和美金刚)仅具有对症治疗作用,且疗效有限。因此,开发有可能改变疾病进程的药物一直是研究的重点。针对淀粉样β蛋白的治疗方法已经成为近30年来的研究焦点。然而,一些前景看好的药物最近在III期临床试验中未能显示出临床疗效。即使百健公司关于阿杜卡努单抗的阳性研究结果也并不完全明确,还需要更多数据来证实其有效性。因此,研究人员将精力转向了针对tau蛋白的治疗方法,因为与淀粉样β蛋白相比,tau蛋白似乎与认知功能下降的严重程度具有更强的相关性。目前,大多数处于临床试验阶段的抗tau药物都是免疫疗法,且都处于临床研究的早期阶段。截至目前,四种抗tau单克隆抗体(戈苏瑞单抗、替拉韦单抗、塞莫瑞单抗和扎戈替单抗)和一种抗tau疫苗(AADvac1)已进入II期临床试验。在本综述中,我们讨论了在临床试验中测试的潜在疾病修饰药物,并更新了仍在临床评估中的药物信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验