Passive anti-amyloid β immunotherapy in Alzheimer's disease—opportunities and challenges

Michael T Heneka, David Morgan, Frank Jessen
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Abstract

With the advent of the first disease-modifying, anti-amyloid β-directed passive immunotherapy for Alzheimer's disease, questions arise who, when, and how to treat. This paper describes shortly the pathogenic basis of and preclinical data, which have, more than two decades ago, initiated the development of this vaccination therapy. We discuss clinical trial results of aducanumab, lecanemab, and donanemab. We also review appropriate use recommendations of these novel treatments on patient selection and safety monitoring. Furthermore, estimations of numbers of patient who will qualify for treatment regarding inclusion and exclusion criteria and estimations on readiness of health-care systems for identifying the right patients and for providing the treatment are reported. In our view, we are experiencing a fundamental shift from syndrome-based Alzheimer's dementia care to early, biomarker-guided treatment of Alzheimer's disease. This shift requires substantial adjustments of infrastructure and resources, but also holds promise of eventually achieving substantial slowing of disease progression and delaying dementia.
阿尔茨海默病的被动抗淀粉样蛋白 β 免疫疗法--机遇与挑战
随着第一种治疗阿尔茨海默病的抗淀粉样蛋白 β 被动免疫疗法的问世,治疗对象、治疗时间和治疗方法等问题也随之而来。本文简要介绍了这种疫苗疗法的致病基础和临床前数据,二十多年前,这些数据启动了这种疗法的开发。我们将讨论阿杜单抗、莱卡内单抗和多那单抗的临床试验结果。我们还回顾了这些新型疗法在患者选择和安全监测方面的合理使用建议。此外,我们还报告了根据纳入和排除标准对符合治疗条件的患者人数进行的估算,以及对医疗保健系统在识别合适患者和提供治疗方面的准备情况进行的估算。我们认为,我们正在经历从基于综合征的阿尔茨海默氏症痴呆症治疗到生物标记物指导下的阿尔茨海默氏症早期治疗的根本性转变。这一转变需要对基础设施和资源进行重大调整,但也有望最终实现大幅减缓疾病进展和延缓痴呆症的发生。
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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