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多发性硬化症中的髓鞘修复治疗药物。

Remyelinating Pharmacotherapies in Multiple Sclerosis.

机构信息

Department of Neurology Weill Institute for the Neurosciences, University of California, San Francisco, San Francisco, CA, USA.

Department of Ophthalmology, University of California, San Francisco, San Francisco, CA, USA.

出版信息

Neurotherapeutics. 2017 Oct;14(4):894-904. doi: 10.1007/s13311-017-0577-0.

Abstract

We have witnessed major successes in the development of effective immunomodulatory therapies capable of reducing adaptive immune-mediated myelin damage in MS over the last 30 years. However, until it is possible to prevent MS or initiate treatment before it has already caused lesions there is a need to repair myelin damage to prevent further axonal loss. The past decade has brought remarkable advances in our understanding of oligodendrocyte biology and the related search for remyelinating therapies in humans. In this review, we first outline the basic biology of central nervous system myelin and remyelination, including a discussion of the major identified pathways and targets that might help yield CNS remyelinating drugs. In conjunction, we provide an overview of techniques that have helped identify compounds capable of promoting oligodendrocyte precursor cell differentiation and myelination. This includes the methods for both initial in vitro screening and subsequent in vivo confirmation of the target. We then review methods proposed to quantify human remyelination in vivo, including visual evoked potentials and putative imaging modalities. As the remyelination era approaches, with the announcement of the first positive trial in remyelination, we are now tasked with answering new questions regarding patient-specific factors (e.g., age) that may influence the extent and optimal therapeutic window for remyelination.

摘要

在过去的 30 年中,我们见证了在开发能够减少多发性硬化症中适应性免疫介导的髓鞘损伤的有效免疫调节疗法方面的重大成功。然而,在能够预防多发性硬化症或在其已经导致病变之前开始治疗之前,有必要修复髓鞘损伤以防止进一步的轴突损失。在过去的十年中,我们对少突胶质细胞生物学的理解以及在人类中寻找髓鞘修复疗法方面取得了显著的进展。在这篇综述中,我们首先概述了中枢神经系统髓鞘和髓鞘修复的基本生物学,包括讨论可能有助于产生中枢神经系统髓鞘修复药物的主要鉴定途径和靶点。同时,我们还概述了有助于鉴定能够促进少突胶质前体细胞分化和髓鞘形成的化合物的技术。这包括用于体外初始筛选和随后体内靶标确认的方法。然后,我们回顾了用于在体内量化人类髓鞘修复的方法,包括视觉诱发电位和潜在的成像方式。随着髓鞘修复时代的到来,随着第一个髓鞘修复阳性试验的宣布,我们现在面临着回答有关影响髓鞘修复程度和最佳治疗窗的患者特定因素(例如年龄)的新问题。

相似文献

1
Remyelinating Pharmacotherapies in Multiple Sclerosis.多发性硬化症中的髓鞘修复治疗药物。
Neurotherapeutics. 2017 Oct;14(4):894-904. doi: 10.1007/s13311-017-0577-0.
6
Remyelinating strategies in multiple sclerosis.多发性硬化症中的再髓鞘化策略。
Expert Rev Neurother. 2014 Nov;14(11):1315-34. doi: 10.1586/14737175.2014.969241.

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