在多发性硬化症的治疗中,疾病修饰疗法诱导或加重其他免疫介导的疾病

S. Baghbanian, M. Sahraian
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引用次数: 2

摘要

干扰素-β(IFN-β)和醋酸格拉默(GA)是干扰复发-缓解型多发性硬化症(RRMS)的主要治疗性免疫调节剂,也是最常用的药物。据报道,INF-β给药后会诱发或加重其他免疫介导的疾病。我们对报告的病例进行了审查,以告知治疗医生这些罕见的不良事件。尽管多发性硬化症患者存在共病性自身免疫性疾病的报道,但疾病修饰药物,尤其是INF-β的促炎作用可能会影响并增强这种共病性。临床或实验室自身免疫史表明,使用GA而不是INF-β作为治疗的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction or aggravation of other immune-mediated disorders by disease-modifying therapy in treatment of multiple sclerosis
Interferon beta (IFN-β) and glatiramer acetate (GA) are the primary therapeutic immunomodulatory agents that interfere with relapsing-remitting multiple sclerosis (RRMS), and the most commonly-used drugs as well. Induction or aggravation of other immune-mediated diseases has been reported following INF-β administration. We have reviewed the reported cases to notify the treating physicians about these rare adverse events. Although co-morbid autoimmune disorders have been reported in patients with MS, the pro-inflammatory role of disease-modifying drugs, especially INF-β, could affect and enhance this co-occurrence. Clinical or laboratory autoimmunity histories suggest the use of GA over INF-β as the treatment of choice.
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来源期刊
Iranian Journal of Neurology
Iranian Journal of Neurology CLINICAL NEUROLOGY-
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