抗淀粉样蛋白单克隆抗体治疗阿尔茨海默病

IF 5.4 2区 医学 Q1 IMMUNOLOGY
BioDrugs Pub Date : 2024-01-01 Epub Date: 2023-11-13 DOI:10.1007/s40259-023-00633-2
Jeffrey Cummings, Amanda M Leisgang Osse, Davis Cammann, Jayde Powell, Jingchun Chen
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引用次数: 0

摘要

aducanumab和lecanemab两种单克隆抗体(mab)已获得美国FDA的加速批准,可用于已证实具有β-淀粉样蛋白病理(Aβ)的早期阿尔茨海默病患者的起始治疗。其中一种单克隆抗体lecanemab随后获得了全面批准,其他单克隆抗体正准备进行积极的审查和批准。抗淀粉样蛋白单克隆抗体具有淀粉样蛋白正电子发射断层扫描显示的显著减少总脑a β的特征。与减缓认知能力下降相关的试验已经实现了可测量斑块a β在15-25厘体范围内的减少;未达到这一阈值的药物的试验与认知益处无关。单克隆抗体在滴定计划、淀粉样蛋白相关成像异常(ARIA)的MRI监测计划以及持续治疗与中断治疗方面存在差异。单克隆抗体观察到的大约30%的衰退减缓,在延长认知完整性和延缓阿尔茨海默病更严重的痴呆期发作方面具有临床意义。这些药物的批准开启了阿尔茨海默病治疗具有疾病修饰特性的新时代。需要进一步的进展,即更大的疗效、更高的安全性、更大的便利性,以及更好地理解脑容量损失等不理解的观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-Amyloid Monoclonal Antibodies for the Treatment of Alzheimer's Disease.

Anti-Amyloid Monoclonal Antibodies for the Treatment of Alzheimer's Disease.

Two monoclonal antibodies (mAbs), aducanumab and lecanemab, have received accelerated approval from the US FDA for initiation of treatment in early Alzheimer's disease patients who have proven β-amyloid pathology (Aβ). One of these, lecanemab, has subsequently received full approval and other monoclonal antibodies are poised for positive review and approval. Anti-amyloid mAbs share the feature of producing a marked reduction in total brain Aβ revealed by amyloid positron emission tomography. Trials associated with slowing of cognitive decline have achieved a reduction in measurable plaque Aβ in the range of 15-25 centiloids; trials of agents that did not reach this threshold were not associated with cognitive benefit. mAbs have differences in terms of titration schedules, MRI monitoring schedules for amyloid-related imaging abnormalities (ARIA), and continuing versus interrupted therapy. The approximate 30% slowing of decline observed with mAbs is clinically meaningful in terms of extended cognitive integrity and delay of onset of the more severe dementia phases of Alzheimer's disease. Approval of these agents initiates a new era in Alzheimer's disease therapeutics with disease-modifying properties. Further advances are needed, i.e. greater efficacy, improved safety, enhanced convenience, and better understanding of ill-understood observations such as brain volume loss.

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来源期刊
BioDrugs
BioDrugs 医学-免疫学
CiteScore
12.60
自引率
2.90%
发文量
50
审稿时长
>12 weeks
期刊介绍: An essential resource for R&D professionals and clinicians with an interest in biologic therapies. BioDrugs covers the development and therapeutic application of biotechnology-based pharmaceuticals and diagnostic products for the treatment of human disease. BioDrugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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