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多发性硬化症的抗原特异性治疗模式:过去、现在和未来。

Antigen-Specific Treatment Modalities in MS: The Past, the Present, and the Future.

机构信息

Laboratory of Experimental Hematology, Vaccine and Infectious Disease Institute (VaxInfectio), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Division of Neurology, Antwerp University Hospital, Edegem, Belgium.

出版信息

Front Immunol. 2021 Feb 19;12:624685. doi: 10.3389/fimmu.2021.624685. eCollection 2021.

DOI:10.3389/fimmu.2021.624685
PMID:33679769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7933447/
Abstract

Antigen-specific therapy for multiple sclerosis may lead to a more effective therapy by induction of tolerance to a wide range of myelin-derived antigens without hampering the normal surveillance and effector function of the immune system. Numerous attempts to restore tolerance toward myelin-derived antigens have been made over the past decades, both in animal models of multiple sclerosis and in clinical trials for multiple sclerosis patients. In this review, we will give an overview of the current approaches for antigen-specific therapy that are in clinical development for multiple sclerosis as well provide an insight into the challenges for future antigen-specific treatment strategies for multiple sclerosis.

摘要

多发性硬化症的抗原特异性治疗可能通过诱导对广泛的髓鞘衍生抗原的耐受性而导致更有效的治疗,而不会损害免疫系统的正常监测和效应功能。在过去的几十年中,无论是在多发性硬化症的动物模型中还是在多发性硬化症患者的临床试验中,人们都尝试了无数次来恢复对髓鞘衍生抗原的耐受性。在这篇综述中,我们将概述目前正在临床开发用于多发性硬化症的抗原特异性治疗方法,并深入了解多发性硬化症的未来抗原特异性治疗策略所面临的挑战。

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Tolerogenic dendritic cell-based treatment for multiple sclerosis (MS): a harmonised study protocol for two phase I clinical trials comparing intradermal and intranodal cell administration.基于耐受性树突状细胞的多发性硬化症(MS)治疗:两项比较皮内和结内细胞给药的I期临床试验的统一研究方案。
BMJ Open. 2019 Sep 9;9(9):e030309. doi: 10.1136/bmjopen-2019-030309.
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Antigen-specific tolerance to self-antigens in protein replacement therapy, gene therapy and autoimmunity.蛋白质替代疗法、基因治疗和自身免疫中针对自身抗原的抗原特异性耐受。
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神经胶质细胞通讯中的外泌体:神经退行性变综述
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Engineering chimeric autoantibody receptor T cells for targeted B cell depletion in multiple sclerosis model: An study.工程化嵌合自身抗体受体T细胞用于多发性硬化症模型中的靶向B细胞耗竭:一项研究。
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Multiple Sclerosis: New Insights into Molecular Pathogenesis and Novel Platforms for Disease Treatment.多发性硬化症:分子发病机制的新见解和疾病治疗的新平台。
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Mechanisms of antigen-induced reversal of CNS inflammation in experimental demyelinating disease.抗原诱导实验性脱髓鞘疾病中枢神经系统炎症逆转的机制。
Sci Adv. 2023 Mar;9(9):eabo2810. doi: 10.1126/sciadv.abo2810. Epub 2023 Mar 1.
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Enhancing the functionality of self-assembled immune signals using chemical crosslinks.利用化学交联增强自组装免疫信号的功能。
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Clinical and immunological control of experimental autoimmune encephalomyelitis by tolerogenic dendritic cells loaded with MOG-encoding mRNA.
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J Neuroimmunol. 2019 Aug 15;333:476953. doi: 10.1016/j.jneuroim.2019.04.013. Epub 2019 May 9.
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