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[多发性硬化症的免疫调节治疗]

[Immunomodulatory therapy in multiple sclerosis].

作者信息

Csépány Tünde, Bereczki Dániel

机构信息

Debreceni Egyetem, Altalános Orvostudományi Kar, Neurológiai Klinika, Debrecen.

出版信息

Ideggyogy Sz. 2004 Nov 20;57(11-12):401-16.

Abstract

During the past decade, several disease-modifying agents have been established and have become available for the treatment of multiple sclerosis. The disease-modifying agents could be grouped into immunomodulatory and immunosuppressive therapies altering the long-term course of multiple sclerosis. Therapy is now available for relapsing-remitting, secondary progressive and progressive-relapsing multiple sclerosis. Different disease-modifying agents became also available for the treatment of relapsing-remitting multiple sclerosis in Hungary which makes the therapeutic decision difficult. This overview might help to give an answer for different questions in the management of multiple sclerosis: Which agent to choose? When to initiate the therapy? Which dose to apply? Are the drugs safe? How long to treat the patients with immunomodulatory drugs? We give a review from the literature to assess the efficacy of disease-modifying therapies and to compare the data from phase three trials of interferon beta1b, two preparations of interferon beta1a or glatiramer acetate for the treatment of multiple sclerosis. We analyzed the efficacy and safety of these agents on physical, inflammatory and cognitive measures of disease activity. Comparison of study results indicated similar effects of immunomodulatory agents on relapse-related and inflammatory measures in relapsing multiple sclerosis. Interferon beta1a slowed the progression of disability in relapsing multiple sclerosis. One interferon beta1a preparation (intramuscularly injected) demonstrated efficacy in slowing progression of cognitive dysfunction. The interferons reduced relapses at early phase of secondary progressive multiple sclerosis, but their efficacy have not yet been proven in the later phase of secondary progressive multiple sclerosis without relapses. Mitoxantrone demonstrated efficacy in slowing the progression of disability in secondary progressive multiple sclerosis. All of the disease modifying agents are safe and tolerable, if the indication is correct and the patients are strictly controlled.

摘要

在过去十年中,已经确立了几种疾病修正药物,并且可用于治疗多发性硬化症。疾病修正药物可分为免疫调节疗法和免疫抑制疗法,它们改变了多发性硬化症的长期病程。目前已有针对复发缓解型、继发进展型和进展复发型多发性硬化症的治疗方法。在匈牙利,也有不同的疾病修正药物可用于治疗复发缓解型多发性硬化症,这使得治疗决策变得困难。本综述可能有助于回答多发性硬化症管理中的不同问题:选择哪种药物?何时开始治疗?应用何种剂量?药物是否安全?用免疫调节药物治疗患者多长时间?我们从文献中进行综述,以评估疾病修正疗法的疗效,并比较干扰素β1b、两种干扰素β1a制剂或醋酸格拉替雷治疗多发性硬化症的三期试验数据。我们分析了这些药物在疾病活动的身体、炎症和认知指标方面的疗效和安全性。研究结果的比较表明,免疫调节药物在复发型多发性硬化症的复发相关和炎症指标方面有相似的效果。干扰素β1a减缓了复发型多发性硬化症中残疾的进展。一种干扰素β1a制剂(肌肉注射)在减缓认知功能障碍进展方面显示出疗效。干扰素在继发进展型多发性硬化症的早期阶段减少了复发,但在继发进展型多发性硬化症无复发的后期阶段,其疗效尚未得到证实。米托蒽醌在减缓继发进展型多发性硬化症中残疾的进展方面显示出疗效。如果适应症正确且对患者进行严格控制,所有疾病修正药物都是安全且可耐受的。

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