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Immunotherapeutic Approaches Targeting Amyloid-β α-Synuclein and Tau for the Treatment of Neurodegenerative Disorders

机译:靶向β-淀粉样蛋白α-突触核蛋白和Tau蛋白的免疫治疗方法可治疗神经退行性疾病

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摘要

Disease-modifying alternatives are sorely needed for the treatment of neurodegenerative disorders, a group of diseases that afflict approximately 50 million Americans annually. Immunotherapy is one of the most developed approaches in this direction. Vaccination against amyloid-β, α-synuclein, or tau has been extensively explored, specially as the discovery that these proteins may propagate cell-to-cell and be accessible to antibodies when embedded into the plasma membrane or in the extracellular space. Likewise, the use of passive immunization approaches with specific antibodies against abnormal conformations of these proteins has also yielded promising results. The clinical development of immunotherapies for Alzheimer’s disease, Parkinson’s disease, frontotemporal dementia, dementia with Lewy bodies, and other neurodegenerative disorders is a field in constant evolution. Results to date suggest that immunotherapy is a promising therapeutic approach for neurodegenerative diseases that progress with the accumulation and prion-like propagation of toxic protein aggregates. Here we provide an overview of the most novel and relevant immunotherapeutic advances targeting amyloid-β in Alzheimer’s disease, α-synuclein in Alzheimer’s disease and Parkinson’s disease, and tau in Alzheimer’s disease and frontotemporal dementia.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-015-0397-z) contains supplementary material, which is available to authorized users.
机译:急需治疗疾病的替代品来治疗神经退行性疾病,这是一种每年折磨约5000万美国人的疾病。免疫疗法是朝着这个方向发展的最先进的方法之一。针对淀粉样蛋白-β,α-突触核蛋白或tau蛋白的疫苗接种已得到广泛研究,特别是因为发现这些蛋白嵌入质膜或细胞外空间后可能会在细胞之间传播,并且抗体可及。同样,使用针对这些蛋白质异常构象的特异性抗体的被动免疫方法也产生了可喜的结果。阿尔茨海默氏病,帕金森氏病,额颞痴呆,路易体痴呆和其他神经退行性疾病的免疫疗法的临床发展是一个不断发展的领域。迄今为止的结果表明,免疫疗法是一种针对神经退行性疾病的有前途的治疗方法,随着有毒蛋白质聚集体的积累和病毒的传播而发展。本文概述了针对阿尔茨海默氏病中的淀粉样蛋白β,阿尔茨海默氏病和帕金森氏病中的α-突触核蛋白以及阿尔茨海默氏病和额颞痴呆中的tau的最新颖和相关的免疫治疗进展。电子补充材料:10.1007 / s13311-015-0397-z)包含补充材料,授权用户可以使用。

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