Suppr超能文献

在多发性硬化症中保护少突胶质细胞并增强髓鞘再生的策略。

Strategies for protecting oligodendrocytes and enhancing remyelination in multiple sclerosis.

作者信息

Rodgers Jane M, Robinson Andrew P, Miller Stephen D

机构信息

Department of Microbiology-Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, 303 E. Chicago Ave., Chicago, Illinois 60611, USA.

出版信息

Discov Med. 2013 Aug;16(86):53-63.

Abstract

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) characterized by encephalitogenic leukocyte infiltration and multifocal plaques of demyelination. Patients present with debilitating clinical sequelae including motor, sensory, and cognitive deficits. For the past 30 years, immune modulating treatments have entered the marketplace and continue to improve in limiting the frequency and severity of relapses, but no cure has been found and no drug has successfully stopped chronic progressive disease. Recent work focusing on the oligodendrocyte, the myelin-producing cell, has provided needed insight into the process of demyelination, the spontaneous ability of the CNS to regenerate, and the inevitable failure of remyelination. From this a number of promising molecular targets have been identified to protect oligodendrocytes and promote remyelination. Combining immunomodulatory therapy with strategies to protect oligodendrocytes from further degeneration and enhance remyelination presents a very real means to improve clinical outcome for chronic progressive patients in the near future. Here we lay out a combination therapy approach to treating MS and survey the current literature on promising drug candidates potentially capable of mediating oligodendrocyte protection and enhancing remyelination.

摘要

多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎症性脱髓鞘疾病,其特征为致脑炎性白细胞浸润和多灶性脱髓鞘斑块。患者会出现使人衰弱的临床后遗症,包括运动、感觉和认知缺陷。在过去30年里,免疫调节治疗已进入市场,并且在限制复发频率和严重程度方面持续改善,但尚未找到治愈方法,也没有药物成功阻止慢性进行性疾病。最近针对少突胶质细胞(产生髓磷脂的细胞)的研究工作,为脱髓鞘过程、CNS的自发再生能力以及髓鞘再生的必然失败提供了必要的见解。由此确定了一些有前景的分子靶点,以保护少突胶质细胞并促进髓鞘再生。将免疫调节疗法与保护少突胶质细胞免于进一步退化并增强髓鞘再生的策略相结合,是在不久的将来改善慢性进行性患者临床结局的一种切实可行的方法。在此,我们阐述一种治疗MS的联合治疗方法,并综述当前有关可能能够介导少突胶质细胞保护和增强髓鞘再生的有前景候选药物的文献。

相似文献

2
The role of oligodendrocytes and oligodendrocyte progenitors in CNS remyelination.
Adv Exp Med Biol. 1999;468:183-97. doi: 10.1007/978-1-4615-4685-6_15.
3
Remyelination: the true regeneration of the central nervous system.
J Comp Pathol. 2013 Aug-Oct;149(2-3):242-54. doi: 10.1016/j.jcpa.2013.05.004. Epub 2013 Jul 5.
4
Oligodendrocyte regeneration: Its significance in myelin replacement and neuroprotection in multiple sclerosis.
Neuropharmacology. 2016 Nov;110(Pt B):633-643. doi: 10.1016/j.neuropharm.2015.10.010. Epub 2015 Oct 22.
5
Targeting CXCR7/ACKR3 as a therapeutic strategy to promote remyelination in the adult central nervous system.
J Exp Med. 2014 May 5;211(5):791-9. doi: 10.1084/jem.20131224. Epub 2014 Apr 14.
6
Mechanisms of remyelination: recent insight from experimental models.
Biomol Concepts. 2014 Aug;5(4):289-98. doi: 10.1515/bmc-2014-0015.
7
Enhancing remyelination in disease--can we wrap it up?
Brain. 2011 Jul;134(Pt 7):1882-900. doi: 10.1093/brain/awr014. Epub 2011 Apr 19.
8
Remyelination in multiple sclerosis: cellular mechanisms and novel therapeutic approaches.
J Neurosci Res. 2015 May;93(5):687-96. doi: 10.1002/jnr.23493. Epub 2014 Oct 7.
9
Recent Advances on Immunosuppressive Drugs and Remyelination Enhancers for the Treatment of Multiple Sclerosis.
Curr Pharm Des. 2021 Oct 5;27(30):3273-3280. doi: 10.2174/1381612827666210127121829.
10
Cellular approaches for stimulating CNS remyelination.
Regen Med. 2007 Sep;2(5):817-29. doi: 10.2217/17460751.2.5.817.

引用本文的文献

1
Hypoxia in multiple sclerosis.
Redox Biol. 2025 Jun;83:103666. doi: 10.1016/j.redox.2025.103666. Epub 2025 May 6.
2
AA147 Alleviates Symptoms in a Mouse Model of Multiple Sclerosis by Reducing Oligodendrocyte Loss.
Glia. 2025 Jun;73(6):1241-1257. doi: 10.1002/glia.70001. Epub 2025 Feb 10.
5
Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome.
Cells. 2022 Apr 8;11(8):1260. doi: 10.3390/cells11081260.
7
Oxidative stress and impaired oligodendrocyte precursor cell differentiation in neurological disorders.
Cell Mol Life Sci. 2021 May;78(10):4615-4637. doi: 10.1007/s00018-021-03802-0. Epub 2021 Mar 10.
8
Pre-clinical and Clinical Implications of "Inside-Out" vs. "Outside-In" Paradigms in Multiple Sclerosis Etiopathogenesis.
Front Cell Neurosci. 2020 Oct 27;14:599717. doi: 10.3389/fncel.2020.599717. eCollection 2020.
10
Corrigendum: Confused Connections? Targeting White Matter to Address Treatment Resistant Schizophrenia.
Front Pharmacol. 2018 Dec 4;9:1417. doi: 10.3389/fphar.2018.01417. eCollection 2018.

本文引用的文献

1
Antigen-specific tolerance by autologous myelin peptide-coupled cells: a phase 1 trial in multiple sclerosis.
Sci Transl Med. 2013 Jun 5;5(188):188ra75. doi: 10.1126/scitranslmed.3006168.
2
3
Generation of oligodendroglial cells by direct lineage conversion.
Nat Biotechnol. 2013 May;31(5):434-9. doi: 10.1038/nbt.2564. Epub 2013 Apr 14.
5
PDGF is required for remyelination-promoting IgM stimulation of oligodendrocyte progenitor cell proliferation.
PLoS One. 2013;8(2):e55149. doi: 10.1371/journal.pone.0055149. Epub 2013 Feb 1.
7
Current status of myelin replacement therapies in multiple sclerosis.
Prog Brain Res. 2012;201:219-31. doi: 10.1016/B978-0-444-59544-7.00011-1.
9
Immunization with a peptide of Semliki Forest virus promotes remyelination in experimental autoimmune encephalomyelitis.
Brain Res. 2012 Dec 7;1488:92-103. doi: 10.1016/j.brainres.2012.09.038. Epub 2012 Sep 29.
10
Progesterone down-regulates spinal cord inflammatory mediators and increases myelination in experimental autoimmune encephalomyelitis.
Neuroscience. 2012 Dec 13;226:40-50. doi: 10.1016/j.neuroscience.2012.09.032. Epub 2012 Sep 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验