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针对阿尔茨海默病中淀粉样β和tau 寡聚体的被动免疫疗法。

Passive Immunotherapies Targeting Amyloid Beta and Tau Oligomers in Alzheimer's Disease.

机构信息

Center for Biomedical Engineering, Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131; Department of Chemistry and Biochemistry, University of Colorado at Colorado Springs, Colorado Springs, Colorado 80918.

Center for Biomedical Engineering, Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131; Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, New Mexico 87131.

出版信息

J Pharm Sci. 2020 Jan;109(1):68-73. doi: 10.1016/j.xphs.2019.10.024. Epub 2019 Oct 21.

Abstract

Alzheimer's disease (AD) is historically difficult to treat, in part because of the inaccessible nature of brain pathology. Amyloid beta and tau proteins drive pathology by forming toxic oligomers that eventually deposit as insoluble amyloid plaques and neurofibrillary tangles. Recent clinical studies suggest that effective drugs must specifically target oligomers, not native monomers or insoluble fibrils. Passive immunotherapy is a promising pharmaceutical strategy used to specifically target these oligomers in situ. Using the specificity of antibodies coupled with the natural power of the body's immune response, this treatment provides an opportunity for safe clearance of pathogenic protein species from the brain. Passive immunotherapies against amyloid beta and tau oligomers have progressed to clinical trials, with many currently in progress. Biochemical studies of antibody-oligomer complexes have helped identify previously unknown toxic epitopes, thus providing knowledge to the AD field as a whole. This mini-review focuses on the efforts to develop passive immunotherapy treatments for AD and discusses the knowledge gained from recent failures and clinical trials in progress.

摘要

阿尔茨海默病(AD)的治疗历来具有挑战性,部分原因是大脑病理学难以触及。淀粉样蛋白β和tau 蛋白通过形成毒性寡聚体而驱动病理学,最终沉积为不溶性淀粉样斑块和神经原纤维缠结。最近的临床研究表明,有效的药物必须专门针对寡聚体,而不是天然单体或不溶性原纤维。被动免疫疗法是一种有前途的药物策略,用于在原位特异性靶向这些寡聚体。利用抗体的特异性结合机体免疫反应的自然能力,这种治疗为安全清除大脑中的致病性蛋白提供了机会。针对淀粉样蛋白β和 tau 寡聚体的被动免疫疗法已进入临床试验阶段,目前许多正在进行中。抗体-寡聚体复合物的生化研究有助于鉴定以前未知的毒性表位,从而为整个 AD 领域提供了知识。这篇迷你综述重点介绍了开发 AD 被动免疫疗法的努力,并讨论了最近失败和正在进行的临床试验中获得的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c1e/6937375/8808331fe258/nihms-1543006-f0001.jpg

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