用于治疗多发性硬化症的晚期药物的系统综述:口服合成药物的重点。

Malihe Safavi, Shekoufeh Nikfar, Mohammad Abdollahi
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引用次数: 10

摘要

多发性硬化症(MS)是一种异质性、慢性、衰弱性免疫介导的中枢神经系统(CNS)疾病。根据其复发或进展模式,MS有四种类型,包括复发缓解型(RRMS)、继发性进展型(SPMS)、原发性进展型(PPMS)和进行性复发型(PRMS)。多发性硬化症没有明确的治愈方法,因此药物治疗通常侧重于减缓疾病的进展,控制症状和改善生活质量。目前还没有专门的药物来治疗经前综合症,因此这些患者经常被忽视。在疾病的这一阶段需要新的药物。另一方面,在过去二十年中主导MS市场的注射免疫调节药物提出了依从性和耐受性问题,而口服治疗确实在便利性方面向前迈进了一步。这篇系统综述文章讨论了口服治疗多发性硬化症的新合成小分子药物。我们检索PubMed、Web of Science和Google Scholar,总结了目前关于作用机制的知识,并完成了拉喹莫德、马西替尼和西泊尼莫德的临床试验。数据收集时间为1985年至2015年1月。开发有效的药物治疗多发性硬化症是严重依赖于了解这种复杂的多因素疾病的生物学基础。目前的药物治疗选择主要是免疫调节剂,这些药物是在MS是一种自身免疫性疾病的基础上开发的。新合成的小分子药物如拉喹莫德、马西替尼和西波尼莫德具有不同的作用机制,可以口服而不是注射给药。
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A systematic review of drugs in late-stage development for the treatment of multiple sclerosis: a focus on oral synthetic drugs.

Multiple sclerosis (MS) is a heterogeneous, chronic, debilitating immune-mediated disease of the central nervous system (CNS). There are four types of MS according to their relapsing or progressive pattern that include relapsing-remitting (RRMS), secondary progressive (SPMS), primary progressive (PPMS), and progressive relapsing (PRMS). There is no definite cure for MS, thus medications typically focus on slowing the progression of the disease, managing symptoms and improving the quality of life. There is no specific medication for the management of PPMS and thus these patients are often neglected. New medicines in this phase of the disease are needed. On the other hand injectable immunomodulatory medicines, which dominated the MS market for over the past two decades, raise the issues of adherence and tolerance while oral therapies do offer a step forward in convenience. This systematic review article discusses the emerging synthetic small molecule that administered orally for MS treatment. We searched PubMed, Web of Science and Google Scholar to summaries the present knowledge on mechanism of action, and completed and current clinical trial of laquinimod, masitinib and siponimod. Data were collected from 1985 to January 2015. The development of effective medicines for MS is critically dependent upon understanding the biological basis of this complex multifactorial disease. The current pharmacotherapeuetic options for its treatment are mainly immunomodulators which were developed on the basis that MS is an autoimmune disease. The new synthetic small molecule agents such as laquinimod, masitinib and siponimod with different mechanism of actions can be administered orally rather than by injection.

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