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多发性硬化症治疗的未来。

The future of multiple sclerosis therapy.

作者信息

Kieseier Bernd C, Wiendl Heinz, Hartung Hans-Peter, Stüve Olaf

机构信息

Department of Neurology, Heinrich-Heine University, Moorenstrasse 5, 40225 Duesseldorf, Germany.

出版信息

Pharmacol Res. 2009 Oct;60(4):207-11. doi: 10.1016/j.phrs.2009.03.016. Epub 2009 Apr 5.

DOI:10.1016/j.phrs.2009.03.016
PMID:19717009
Abstract

Multiple sclerosis (MS) represents the prototypic inflammatory autoimmune disorder of the central nervous system and the most common cause of neurological disability in young adults, exhibiting considerable clinical, radiological and pathological heterogeneity. A better understanding of the immunopathological processes underlying this disease have recently led to the design of numerous novel therapeutical approaches. Perhaps most importantly, therapy has changed dramatically over the past decade in that all relapsing forms of MS, including early forms of MS are now being treated relatively aggressively. However, there are still unmet needs in the management of this disease, especially since all of the currently available disease-modifying drugs are only partially effective. Most of the clinically relevant therapeutic agents are not yet available as oral formulations. A substantial number of pivotal and preliminary reports provide encouraging new evidence on advances being made in the development of oral therapies for MS. A different strategy is the development of very potent monoclonal antibodies, given intravenously or subcutaneously, many of which are being examined for clinical efficacy. These agents are potentially more effective, but may carry more serious side effects. Finally, drugs with a known good safety profile are being developed further. These advances are critically reviewed and put into perspective.

摘要

多发性硬化症(MS)是中枢神经系统典型的炎性自身免疫性疾病,也是年轻成年人神经功能障碍最常见的病因,具有显著的临床、放射学和病理学异质性。最近,对该疾病潜在免疫病理过程的深入理解促使人们设计出了众多新型治疗方法。或许最重要的是,在过去十年里治疗方法发生了巨大变化,如今所有复发型MS,包括早期MS都得到了相对积极的治疗。然而,在这种疾病的管理方面仍存在未满足的需求,特别是因为目前所有可用的疾病修正药物都只是部分有效。大多数具有临床相关性的治疗药物尚未有口服制剂。大量关键和初步报告为MS口服疗法开发取得的进展提供了令人鼓舞的新证据。另一种策略是开发非常有效的单克隆抗体,通过静脉注射或皮下注射给药,其中许多正在进行临床疗效研究。这些药物可能更有效,但可能会带来更严重的副作用。最后,具有已知良好安全性的药物正在进一步研发。本文对这些进展进行了批判性综述并给出了相关观点。

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The future of multiple sclerosis therapy.多发性硬化症治疗的未来。
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Canine dorsal root ganglia satellite glial cells represent an exceptional cell population with astrocytic and oligodendrocytic properties.犬背根神经节卫星胶质细胞是一种具有星形胶质细胞和少突胶质细胞特性的特殊细胞群体。
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Neurol Sci. 2016 Apr;37(4):613-22. doi: 10.1007/s10072-016-2519-8. Epub 2016 Feb 19.
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[Teriflunomide for treatment of multiple sclerosis].[特立氟胺用于治疗多发性硬化症]
Nervenarzt. 2013 Jun;84(6):724-31. doi: 10.1007/s00115-013-3779-7.
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Future MS care: a consensus statement of the MS in the 21st Century Steering Group.未来多发性硬化症的治疗:21 世纪多发性硬化症指导小组的共识声明。
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Nat Rev Neurol. 2011 May;7(5):255-62. doi: 10.1038/nrneurol.2011.41. Epub 2011 Apr 5.
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A one-year prospective, randomized, placebo-controlled, quadruple-blinded, phase II safety pilot trial of combination therapy with interferon beta-1a and mycophenolate mofetil in early relapsing-remitting multiple sclerosis (TIME MS).一项为期一年的前瞻性、随机、安慰剂对照、四重盲、II 期安全性先导试验,研究干扰素 β-1a 和霉酚酸酯联合治疗早期复发缓解型多发性硬化症(TIME MS)。
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