亨廷顿氏症的新兴抗体疗法:现状与未来发展前景。

IF 3.4 2区 医学 Q2 CLINICAL NEUROLOGY Expert Review of Neurotherapeutics Pub Date : 2024-03-01 Epub Date: 2024-02-07 DOI:10.1080/14737175.2024.2314183
Anamaria Jurcau, Aurel Simion, Maria Carolina Jurcau
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引用次数: 0

摘要

导言:亨廷顿氏病(Huntington's disease,HD)是一种遗传性神经退行性疾病,具有可识别的基因缺陷,适合早期干预,甚至可能在症状出现前就进行干预。我们最近在阐明亨廷顿氏病发病机制方面取得的进展揭示了一系列新的潜在治疗靶点,其中免疫疗法正在临床前实验中积极探索:本综述重点关注目前在体外和动物实验中评估的针对各种表位(突变亨廷蛋白和磷酸化 tau)的抗体疗法的潜力。本综述中使用的参考文献是从PubMed数据库中检索HD免疫疗法的,并对临床试验登记册中已在临床试验中进行评估的分子进行了审查:基于抗体的疗法在一系列以异常折叠蛋白聚集沉积为特征的神经退行性疾病(包括HD)中引起了广泛关注。体内抗体和纳米抗体可与神经细胞内的突变杭汀蛋白相互作用。然而,使用其中一些内抗体所获得的结果相互矛盾,这凸显了正确选择表位和开发更接近人类疾病的动物模型的必要性。这些策略的批准将需要医疗保健系统在财政和后勤方面做出巨大努力。
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Emerging antibody-based therapies for Huntington's disease: current status and perspectives for future development.

Introduction: Being an inherited neurodegenerative disease with an identifiable genetic defect, Huntington's disease (HD) is a suitable candidate for early intervention, possibly even in the pre-symptomatic stage. Our recent advances in elucidating the pathogenesis of HD have revealed a series of novel potential therapeutic targets, among which immunotherapies are actively pursued in preclinical experiments.

Areas covered: This review focuses on the potential of antibody-based treatments targeting various epitopes (of mutant huntingtin as well as phosphorylated tau) that are currently evaluated in vitro and in animal experiments. The references used in this review were retrieved from the PubMed database, searching for immunotherapies in HD, and clinical trial registries were reviewed for molecules already evaluated in clinical trials.

Expert opinion: Antibody-based therapies have raised considerable interest in a series of neurodegenerative diseases characterized by deposition of aggregated of aberrantly folded proteins, HD included. Intrabodies and nanobodies can interact with mutant huntingtin inside the nervous cells. However, the conflicting results obtained with some of these intrabodies highlight the need for proper choice of epitopes and for developing animal models more closely mimicking human disease. Approval of these strategies will require a considerable financial and logistic effort on behalf of healthcare systems.

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来源期刊
Expert Review of Neurotherapeutics
Expert Review of Neurotherapeutics Medicine-Neurology (clinical)
CiteScore
7.00
自引率
2.30%
发文量
61
审稿时长
4-8 weeks
期刊介绍: Expert Review of Neurotherapeutics (ISSN 1473-7175) provides expert reviews on the use of drugs and medicines in clinical neurology and neuropsychiatry. Coverage includes disease management, new medicines and drugs in neurology, therapeutic indications, diagnostics, medical treatment guidelines and neurological diseases such as stroke, epilepsy, Alzheimer''s and Parkinson''s. Comprehensive coverage in each review is complemented by the unique Expert Review format and includes the following sections: Expert Opinion - a personal view of the data presented in the article, a discussion on the developments that are likely to be important in the future, and the avenues of research likely to become exciting as further studies yield more detailed results Article Highlights – an executive summary of the author’s most critical points
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