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用于治疗多发性硬化症的疾病修饰药物:最新进展与未来展望

Disease-modifying agents for multiple sclerosis: recent advances and future prospects.

作者信息

Menge Til, Weber Martin S, Hemmer Bernhard, Kieseier Bernd C, von Büdingen Hans-Christian, Warnke Clemens, Zamvil Scott S, Boster Aaron, Khan Omar, Hartung Hans-Peter, Stüve Olaf

机构信息

Department of Neurology, Heinrich Heine-University, Düsseldorf, Germany.

出版信息

Drugs. 2008;68(17):2445-68. doi: 10.2165/0003495-200868170-00004.

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disease of the CNS. Currently, six medications are approved for immunmodulatory and immunosuppressive treatment of the relapsing disease course and secondary-progressive MS. In the first part of this review, the pathogenesis of MS and its current treatment options are discussed. During the last decade, our understanding of autoimmunity and the pathogenesis of MS has advanced substantially. This has led to the development of a number of compounds, several of which are currently undergoing clinical testing in phase II and III studies. While current treatment options are only available for parenteral administration, several oral compounds are now in clinical trials, including the immunosuppressive agents cladribine and laquinimod. A novel mode of action has been described for fingolimod, another orally available agent, which inhibits egress of activated lymphocytes from draining lymph nodes. Dimethylfumarate exhibits immunomodulatory as well as immunosuppressive activity when given orally. All of these compounds have successfully shown efficacy, at least in regards to the surrogate marker contrast-enhancing lesions on magnetic resonance imaging. Another class of agents that is highlighted in this review are biological agents, namely monoclonal antibodies (mAb) and recombinant fusion proteins. The humanized mAb daclizumab inhibits T-lymphocyte activation via blockade of the interleukin-2 receptor. Alemtuzumab and rituximab deplete leukocytes and B cells, respectively; the fusion protein atacicept inhibits specific B-cell growth factors resulting in reductions in B-cells and plasma cells. These compounds are currently being tested in phase II and III studies in patients with relapsing MS. The concept of neuro-protection and -regeneration has not advanced to a level where specific compounds have entered clinical testing. However, several agents approved for conditions other than MS are highlighted. Finally, with the advent of these highly potent novel therapies, rare, but potentially serious adverse effects have been noted, namely infections and malignancies. These are critically reviewed and put into perspective.

摘要

多发性硬化症(MS)是一种中枢神经系统的慢性自身免疫性疾病。目前,有六种药物被批准用于复发型病程和继发进展型MS的免疫调节和免疫抑制治疗。在本综述的第一部分,讨论了MS的发病机制及其当前的治疗选择。在过去十年中,我们对自身免疫和MS发病机制的理解有了显著进展。这导致了许多化合物的开发,其中几种目前正在进行II期和III期临床试验。虽然目前的治疗选择仅适用于肠胃外给药,但几种口服化合物目前正在进行临床试验,包括免疫抑制剂克拉屈滨和拉喹莫德。已描述了另一种口服可用药物芬戈莫德的一种新作用模式,它可抑制活化淋巴细胞从引流淋巴结中流出。富马酸二甲酯口服给药时具有免疫调节和免疫抑制活性。所有这些化合物至少在磁共振成像上的替代标志物强化病灶方面已成功显示出疗效。本综述中突出强调的另一类药物是生物制剂,即单克隆抗体(mAb)和重组融合蛋白。人源化mAb达利珠单抗通过阻断白细胞介素-2受体来抑制T淋巴细胞活化。阿仑单抗和利妥昔单抗分别消耗白细胞和B细胞;融合蛋白阿他西普抑制特定的B细胞生长因子,从而导致B细胞和浆细胞减少。这些化合物目前正在复发型MS患者中进行II期和III期试验。神经保护和再生的概念尚未发展到有特定化合物进入临床试验的阶段。然而,有几种被批准用于MS以外病症的药物被突出强调。最后,随着这些高效新疗法的出现,已注意到一些罕见但可能严重的不良反应,即感染和恶性肿瘤。对这些进行了严格审查并进行了客观分析。

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