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多发性硬化症中髓鞘修复治疗的成就与障碍。

Achievements and obstacles of remyelinating therapies in multiple sclerosis.

机构信息

Clinical Neuroimmunology and Neurochemistry, Department of Neurology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany.

Institute of Neuropathology, University Hospital Münster, Pottkamp 2, 48149 Münster, Germany.

出版信息

Nat Rev Neurol. 2017 Dec;13(12):742-754. doi: 10.1038/nrneurol.2017.139. Epub 2017 Nov 17.

Abstract

Remyelination in the CNS is the natural process of damage repair in demyelinating diseases such as multiple sclerosis (MS). However, remyelination becomes inadequate in many people with MS, which results in axonal degeneration and clinical disability. Enhancement of remyelination is a logical therapeutic goal; nevertheless, all currently licensed therapies for MS are immunomodulatory and do not support remyelination directly. Several molecular pathways have been identified as potential therapeutic targets to induce remyelination, and some of these have now been assessed in proof-of-concept clinical trials. However, trial design faces several obstacles: optimal clinical or paraclinical outcome measures to assess remyelination remain ill-defined, and identification of the ideal timing of therapy is also a crucial issue. In addition, realistic expectations are needed concerning the probable benefits of such therapies. Nevertheless, approaches that enhance remyelination are likely to be protective for axons and so could prevent long-term neurodegeneration. Future MS treatment paradigms, therefore, are likely to comprise a combinatorial approach that involves both immunomodulatory and regenerative treatments.

摘要

中枢神经系统的髓鞘再生是脱髓鞘疾病(如多发性硬化症)损伤修复的自然过程。然而,许多多发性硬化症患者的髓鞘再生不足,导致轴突退化和临床残疾。增强髓鞘再生是一个合理的治疗目标;然而,目前所有多发性硬化症的许可疗法都是免疫调节的,不能直接支持髓鞘再生。已经确定了几个分子途径作为诱导髓鞘再生的潜在治疗靶点,其中一些已经在概念验证临床试验中进行了评估。然而,试验设计面临几个障碍:评估髓鞘再生的最佳临床或临床前终点仍未明确,确定治疗的理想时机也是一个关键问题。此外,对于这些疗法可能带来的益处还需要有现实的期望。尽管如此,增强髓鞘再生的方法可能对轴突有保护作用,从而可以防止长期的神经退行性变。因此,未来多发性硬化症的治疗模式可能包括一种组合疗法,既包括免疫调节治疗,也包括再生治疗。

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