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使用脂质体疫苗产生的新型磷酸化tau单克隆抗体,对构象性tau病表位的识别增强。

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

作者信息

Theunis Clara, Adolfsson Oskar, Crespo-Biel Natalia, Piorkowska Kasia, Pihlgren Maria, Hickman David T, Gafner Valérie, Borghgraef Peter, Devijver Herman, Pfeifer Andrea, Van Leuven Fred, Muhs Andreas

机构信息

Experimental Genetics Group - LEGTEGG, Department of Human Genetics, KULeuven, Leuven, Belgium.

AC Immune SA, EPFL Innovation Park, Building B, Lausanne, Switzerland.

出版信息

J Alzheimers Dis. 2017;56(2):585-599. doi: 10.3233/JAD-160695.

DOI:10.3233/JAD-160695
PMID:28035925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5271481/
Abstract

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.

摘要

微管相关蛋白Tau是一种内在无序、极易溶解的神经元蛋白。在仍不明的情况下,Tau蛋白会形成可溶性寡聚体和不溶性聚集体,这些与包括阿尔茨海默病在内的各种脑部病变的病因及进展密切相关。此前我们报道了基于脂质体的疫苗的研发及其在tau蛋白病临床前小鼠模型中的疗效和安全性。在此我们报告使用一种脂质体疫苗来产生具有特定特性的单克隆抗体,这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。通过一系列方法对抗体ACI-5400的特异性和亲和力进行了表征:(i)测量对已知与tau蛋白病相关特定磷酸化Tau表位的选择性,(ii)进行肽和蛋白质结合试验的组合,(iii)对来自小鼠临床前tau蛋白病模型以及代表六种不同tau蛋白病的人类受试者的脑切片进行染色,以及(iv)在非变性夹心试验中评估对tau蛋白病脑提取物上病理表位的选择性结合。我们得出结论,ACI-5400抗体与在S396位点磷酸化的Tau蛋白结合,并倾向于tau蛋白病患者(包括阿尔茨海默病患者)脑中通常存在的构象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/d9785801a5e6/jad-56-jad160695-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/c7886cc22e4a/jad-56-jad160695-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/a969a91bbc80/jad-56-jad160695-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/248d3790be9e/jad-56-jad160695-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/a6243d9c751c/jad-56-jad160695-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/cec6428099a9/jad-56-jad160695-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/2f98778f5d16/jad-56-jad160695-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/d9785801a5e6/jad-56-jad160695-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/c7886cc22e4a/jad-56-jad160695-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/a969a91bbc80/jad-56-jad160695-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/248d3790be9e/jad-56-jad160695-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/a6243d9c751c/jad-56-jad160695-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/cec6428099a9/jad-56-jad160695-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/2f98778f5d16/jad-56-jad160695-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e6e/5271481/d9785801a5e6/jad-56-jad160695-g007.jpg

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