Novel Monoclonal Antibody Specific toward Amyloid-β Binds to a Unique Epitope within the N-Terminal Region

IF 3 Q3 IMMUNOLOGY
Antibodies Pub Date : 2024-08-09 DOI:10.3390/antib13030068
Giavanna Paterno, Brenda D. Moore, Brach M. Bell, Kimberly-Marie M. Gorion, Yong Ran, Stefan Prokop, Todd E. Golde, Benoit I Giasson
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引用次数: 0

Abstract

Amyloid-β (Aβ) deposition throughout the neuroaxis is a classical hallmark of several neurodegenerative diseases, most notably Alzheimer’s disease (AD). Aβ peptides of varied length and diverse structural conformations are deposited within the parenchyma and vasculature in the brains of individuals with AD. Neuropathologically, Aβ pathology can be assessed using antibodies to label and characterize their features, which in turn leads to a more extensive understanding of the pathological process. In the present study, we generated a novel monoclonal antibody, which we found to be specific for the N-terminal region of Aβ. This antibody reacted to amyloid precursor protein expressed in cultured cells and labels Aβ plaques and cerebral amyloid angiopathy in brain tissue from a mouse model of amyloidosis as well as post-mortem brain tissue from patients diagnosed with AD. This highly specific novel antibody will serve as a unique tool for future studies investigating Aβ deposition in novel mouse models and cross-sectional studies using post-mortem human tissue.
特异性淀粉样蛋白-β的新型单克隆抗体与 N 端区域的独特表位结合
淀粉样蛋白-β(Aβ)在整个神经轴的沉积是多种神经退行性疾病的典型特征,其中阿尔茨海默病(AD)最为突出。不同长度和不同结构构象的 Aβ 肽沉积在 AD 患者大脑的实质和血管中。在神经病理学上,Aβ病理学可通过抗体标记和描述其特征进行评估,进而更广泛地了解病理过程。在本研究中,我们生成了一种新型单克隆抗体,发现它对Aβ的N端区域具有特异性。这种抗体能与培养细胞中表达的淀粉样前体蛋白发生反应,并能标记淀粉样蛋白病小鼠模型脑组织中的Aβ斑块和脑淀粉样血管病变,以及确诊为AD患者的死后脑组织。这种高度特异性的新型抗体将成为未来研究新型小鼠模型中 Aβ 沉积和使用死后人体组织进行横断面研究的独特工具。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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