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干扰素 β 在多发性硬化症治疗中的现状和未来作用。

Current and future role of interferon beta in the therapy of multiple sclerosis.

机构信息

Institute of Neurology, University College London, London, United Kingdom.

出版信息

J Interferon Cytokine Res. 2010 Oct;30(10):715-26. doi: 10.1089/jir.2010.0089.

Abstract

Interferon beta was the first specific disease-modifying therapy licensed for multiple sclerosis (MS) and in its many forms remains the most commonly prescribed agent worldwide. It, however, has a modest effect in reducing relapse rates, magnetic resonance imaging activity, and disability, and many patients are unable to tolerate it because of the associated side effects or mode of administration. With the licensing of glatiramer acetate, natalizumab and mitoxantrone as disease-modifying therapies for MS alternative options are available to people with MS. Many exciting new therapies are also in the pipeline, namely, the monoclonal antibodies alemtuzumab, rituximab, and daclizumab and the promising oral agents BG00012, cladribine, fingolimod, laquinimod, and teriflunomide. In this article we review the immunopathology of MS and the proposed mechanisms of action of currently available and anticipated treatments. We also review the efficacy of each drug, use of combination therapy strategies, and the potential role of the interferon beta preparations in the future.

摘要

干扰素 β 是第一种被批准用于多发性硬化症 (MS) 的特异性疾病修正治疗药物,在其多种形式下仍然是全球最常用的处方药物。然而,它在降低复发率、磁共振成像活动和残疾方面的效果有限,而且许多患者因相关副作用或给药方式而无法耐受。随着醋酸格拉替雷、那他珠单抗和米托蒽醌被批准为多发性硬化症的疾病修正治疗药物,MS 患者有了更多的选择。许多令人兴奋的新疗法也在研发中,即单克隆抗体阿仑单抗、利妥昔单抗和达利珠单抗以及有前途的口服药物 BG00012、克拉屈滨、芬戈莫德、拉喹莫德和特立氟胺。本文综述了多发性硬化症的免疫病理学以及现有和预期治疗方法的作用机制。我们还综述了每种药物的疗效、联合治疗策略的应用以及干扰素 β 制剂在未来的潜在作用。

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