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Novel Phospho-Tau Monoclonal Antibody Generated Using a Liposomal Vaccine with Enhanced Recognition of a Conformational Tauopathy Epitope

机译:使用脂质体疫苗生成的新型磷酸化Tau单克隆抗体增强了构象性Tauopathy抗原决定簇的识别

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摘要

The microtubule-associated protein Tau is an intrinsically unfolded, very soluble neuronal protein. Under still unknown circumstances, Tau protein forms soluble oligomers and insoluble aggregates that are closely linked to the cause and progression of various brain pathologies, including Alzheimer’s disease. Previously we reported the development of liposome-based vaccines and their efficacy and safety in preclinical mouse models for tauopathy. Here we report the use of a liposomal vaccine for the generation of a monoclonal antibody with particular characteristics that makes it a valuable tool for fundamental studies as well as a candidate antibody for diagnostic and therapeutic applications. The specificity and affinity of antibody ACI-5400 were characterized by a panel of methods: (i) measuring the selectivity for a specific phospho-Tau epitope known to be associated with tauopathy, (ii) performing a combination of peptide and protein binding assays, (iii) staining of brain sections from mouse preclinical tauopathy models and from human subjects representing six different tauopathies, and (iv) evaluating the selective binding to pathological epitopes on extracts from tauopathy brains in non-denaturing sandwich assays. We conclude that the ACI-5400 antibody binds to protein Tau phosphorylated at S396 and favors a conformation that is typically present in the brain of tauopathy patients, including Alzheimer’s disease.
机译:微管相关蛋白Tau是一种固有的折叠型,非常易溶的神经元蛋白。在仍然未知的情况下,Tau蛋白形成可溶性寡聚物和不溶性聚集体,与各种脑部疾病(包括阿尔茨海默氏病)的病因和进展密切相关。以前,我们报道了基于脂质体的疫苗的开发及其在tauopathy的临床前小鼠模型中的功效和安全性。在这里,我们报告了脂质体疫苗在产生具有特定特征的单克隆抗体中的用途,该单克隆抗体使其成为基础研究的宝贵工具以及诊断和治疗应用的候选抗体。抗体ACI-5400的特异性和亲和力通过一系列方法进行表征:(i)测量对已知与tauopathy有关的特定磷酸Tau表位的选择性,(ii)进行肽和蛋白质结合测定的组合, (iii)对来自小鼠临床前tauopathy模型和代表六个不同tauopathies的人类受试者的脑切片进行染色,以及(iv)在非变性三明治测定法中评估对tauopathy脑提取物的病理表位的选择性结合。我们得出的结论是,ACI-5400抗体与S396处磷酸化的蛋白Tau结合,并有利于tauopathy患者(包括阿尔茨海默氏病)患者大脑中通常存在的构象。

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