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免疫抑制疗法在多发性硬化治疗中的作用。

Role of immunosuppressive therapy for the treatment of multiple sclerosis.

机构信息

Department of Neurology, Brigham and Women's Hospital, Center for Neurologic Disease and Partners MS Center, Harvard Medical School, Boston, MA, USA.

出版信息

Neurotherapeutics. 2013 Jan;10(1):77-88. doi: 10.1007/s13311-012-0172-3.

Abstract

Immunosuppressives have been used in multiple sclerosis (MS) since 1966. Today, we have many treatments for the relapsing forms of the disease, including 8 US Food and Drug Administration-approved therapies, with more soon to be introduced. Given the current treatment landscape what place do immunosuppressants have in combating MS? Trial work and our experience suggest that immunosuppressives still have an important role in treating MS. Cyclophosphamide finds use in treating patients with severe, inflammatory relapsing remitting MS or those suffering from a fulminant attack. We tend to employ mycophenolate mofetil as an add-on to injectable therapy for patients experiencing breakthrough activity. Some progressive (primary progressive multiple sclerosis or secondary progressive multiple sclerosis) patients may stabilize after treatment with either cyclophosphamide or mycophenolate. We rarely employ mitoxantrone because of potential cardiac or carcinogenic effects. We prefer to use cyclophosphamide or mycophenolate mofetil in preference to methotrexate because evidence of efficacy is limited for this drug. We have less experience with azathioprine, but it may be an alternative for patients with limited options who are unable to tolerate conventional therapies.

摘要

免疫抑制剂自 1966 年以来就被用于多发性硬化症(MS)的治疗。如今,我们有许多针对疾病复发形式的治疗方法,包括 8 种美国食品和药物管理局批准的疗法,更多的即将推出。鉴于当前的治疗现状,免疫抑制剂在对抗 MS 方面有什么作用?试验工作和我们的经验表明,免疫抑制剂在治疗 MS 方面仍然具有重要作用。环磷酰胺用于治疗严重的、炎症性的复发缓解型 MS 患者,或那些患有暴发性发作的患者。我们倾向于在注射治疗的基础上添加霉酚酸酯来治疗突破性活动的患者。一些进展型(原发性进展型多发性硬化症或继发性进展型多发性硬化症)患者在接受环磷酰胺或霉酚酸酯治疗后可能会稳定。由于潜在的心脏或致癌作用,我们很少使用米托蒽醌。我们更愿意使用环磷酰胺或霉酚酸酯,而不是甲氨蝶呤,因为这种药物的疗效证据有限。我们对硫唑嘌呤的经验较少,但对于那些无法耐受常规治疗且选择有限的患者来说,它可能是一种替代药物。

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本文引用的文献

1
Risk of natalizumab-associated progressive multifocal leukoencephalopathy.
N Engl J Med. 2012 May 17;366(20):1870-80. doi: 10.1056/NEJMoa1107829.
2
Interferon, azathioprine and corticosteroids in multiple sclerosis: 6-year follow-up of the ASA cohort.
Clin Neurol Neurosurg. 2012 Sep;114(7):940-6. doi: 10.1016/j.clineuro.2012.02.014. Epub 2012 Mar 7.
5
Lights and shadows of cyclophosphamide in the treatment of multiple sclerosis.
Autoimmune Dis. 2011 Mar 15;2011:961702. doi: 10.4061/2011/961702.
7
Progressive multifocal leukoencephalopathy and newer biological agents.
Drug Saf. 2010 Nov 1;33(11):969-83. doi: 10.2165/11537510-000000000-00000.
8
Intrathecal methotrexate treatment in multiple sclerosis.
J Neurol. 2010 Nov;257(11):1806-11. doi: 10.1007/s00415-010-5614-4. Epub 2010 Jun 10.
10
Treatment of neuromyelitis optica with mycophenolate mofetil: retrospective analysis of 24 patients.
Arch Neurol. 2009 Sep;66(9):1128-33. doi: 10.1001/archneurol.2009.175.

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