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本文引用的文献

1
Recommendations for clinical use of data on neutralising antibodies to interferon-beta therapy in multiple sclerosis.多发性硬化症中干扰素-β治疗的中和抗体数据的临床应用建议。
Lancet Neurol. 2010 Jul;9(7):740-50. doi: 10.1016/S1474-4422(10)70103-4.
2
Daclizumab for relapsing remitting multiple sclerosis.达克珠单抗用于复发缓解型多发性硬化症。
Cochrane Database Syst Rev. 2010 Jun 16(6):CD008127. doi: 10.1002/14651858.CD008127.pub2.
3
Cytokine networks in multiple sclerosis: lost in translation.多发性硬化症中的细胞因子网络:翻译中的迷失。
Curr Opin Neurol. 2010 Jun;23(3):205-11. doi: 10.1097/WCO.0b013e3283391feb.
4
Rituximab-associated infections.利妥昔单抗相关感染。
Semin Hematol. 2010 Apr;47(2):187-98. doi: 10.1053/j.seminhematol.2010.01.002.
5
B cells as a target of immune modulation.作为免疫调节靶点的B细胞。
Ann Indian Acad Neurol. 2009 Oct;12(4):221-5. doi: 10.4103/0972-2327.58275.
6
Alemtuzumab and multiple sclerosis: therapeutic application.阿仑单抗与多发性硬化症:治疗应用。
Expert Opin Biol Ther. 2010 Mar;10(3):421-9. doi: 10.1517/14712591003586806.
7
A placebo-controlled trial of oral cladribine for relapsing multiple sclerosis.一项口服克拉屈滨治疗复发型多发性硬化的安慰剂对照试验。
N Engl J Med. 2010 Feb 4;362(5):416-26. doi: 10.1056/NEJMoa0902533. Epub 2010 Jan 20.
8
Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis.口服芬戈莫德或肌肉注射干扰素治疗复发型多发性硬化。
N Engl J Med. 2010 Feb 4;362(5):402-15. doi: 10.1056/NEJMoa0907839. Epub 2010 Jan 20.
9
Multiple sclerosis pharmacogenomics: maximizing efficacy of therapy.多发性硬化症的药物基因组学:最大化治疗效果。
Neurology. 2010 Jan 5;74 Suppl 1:S62-9. doi: 10.1212/WNL.0b013e3181c980fb.
10
Emerging multiple sclerosis oral therapies.新兴多发性硬化症口服疗法。
Neurology. 2010 Jan 5;74 Suppl 1:S47-53. doi: 10.1212/WNL.0b013e3181c97f89.

多发性硬化症:发病机制与治疗。

Multiple sclerosis: pathogenesis and treatment.

机构信息

Department of Neurology, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

出版信息

Curr Neuropharmacol. 2011 Sep;9(3):409-16. doi: 10.2174/157015911796557911.

DOI:10.2174/157015911796557911
PMID:22379455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3151595/
Abstract

Multiple sclerosis (MS) is a chronic inflammatory autoimmune demyelinating disease of the central nervous system. It affects approximately 400,000 people in the United States and onset is usually during young adulthood. There are four clinical forms of MS, of which relapsing remitting type is the most common. As the etiology of MS is unknown, finding a cure will remain challenging. The main mechanism of injury appears to be inflammation and 8 agents are now FDA approved to help control MS. These agents for relapsing forms of MS target different parts of the immune system, with the end goal of decreasing and avoiding further inflammation. No agents are FDA approved for the primary progressive version of MS. FDA approved agents include four preparations of interferon β (Avonex, Rebif, Betaseron and Extavia), glatiramer acetate (Copaxone), mitoxantrone (Novantrone), natalizumab (Tysabri) and fingolimod (Gilenya). There are several drug undergoing phase II and III trials. The heterogeneity of the MS disease process, individual patient response, and medication toxicities continue to challenge the treating physician.

摘要

多发性硬化症(MS)是一种中枢神经系统的慢性炎症性自身免疫脱髓鞘疾病。它影响了美国约 40 万人,发病通常在青年时期。MS 有四种临床形式,其中复发缓解型最常见。由于 MS 的病因不明,寻找治愈方法仍具有挑战性。主要的损伤机制似乎是炎症,目前有 8 种药物获得 FDA 批准用于帮助控制 MS。这些用于治疗复发型 MS 的药物针对免疫系统的不同部位,最终目标是减少和避免进一步的炎症。没有药物获得 FDA 批准用于原发性进行性 MS。获得 FDA 批准的药物包括四种干扰素β制剂(Avonex、Rebif、Betaseron 和 Extavia)、那他珠单抗(Tysabri)、芬戈莫德(Gilenya)。还有几种药物正在进行 II 期和 III 期临床试验。MS 疾病过程的异质性、个体患者的反应和药物毒性继续给治疗医生带来挑战。