Fraunhofer Institute for Cell Therapy and Immunology, Department for Drug Design and Target Validation, 06120 Halle (Saale), Germany.
Probiodrug AG, 06120 Halle (Saale), Germany.
Molecules. 2018 May 3;23(5):1068. doi: 10.3390/molecules23051068.
Passive immunotherapy has emerged as a very promising approach for the treatment of Alzheimer’s disease and other neurodegenerative disorders, which are characterized by the misfolding and deposition of amyloid peptides. On the basis of the amyloid hypothesis, the majority of antibodies in clinical development are directed against amyloid β (Aβ), the primary amyloid component in extracellular plaques. This review focuses on the current status of Aβ antibodies in clinical development, including their characteristics and challenges that came up in clinical trials with these new biological entities (NBEs). Emphasis is placed on the current view of common side effects observed with passive immunotherapy, so-called amyloid-related imaging abnormalities (ARIAs), and potential ways to overcome this issue. Among these new ideas, a special focus is placed on molecules that are directed against post-translationally modified variants of the Aβ peptide, an emerging approach for development of new antibody molecules.
被动免疫疗法已成为治疗阿尔茨海默病和其他神经退行性疾病的一种很有前途的方法,这些疾病的特征是淀粉样肽的错误折叠和沉积。基于淀粉样蛋白假说,大多数处于临床开发阶段的抗体针对的是淀粉样β(Aβ),这是细胞外斑块中主要的淀粉样成分。本综述重点介绍了临床开发中 Aβ 抗体的现状,包括这些新型生物实体(NBEs)临床试验中出现的特征和挑战。重点介绍了被动免疫治疗中观察到的常见副作用,即所谓的淀粉样相关成像异常(ARIA),以及克服这一问题的潜在方法。在这些新理念中,特别关注针对 Aβ肽的翻译后修饰变体的分子,这是开发新抗体分子的一种新兴方法。