Suppr超能文献

多发性硬化症新疗法的识别与开发。

Identification and development of new therapeutics for multiple sclerosis.

作者信息

Linker Ralf A, Kieseier Bernd C, Gold Ralf

机构信息

Department of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Gudrunstrasse 56, 44791 Bochum, Germany.

出版信息

Trends Pharmacol Sci. 2008 Nov;29(11):558-65. doi: 10.1016/j.tips.2008.07.012. Epub 2008 Sep 17.

Abstract

In recent years, large efforts have been undertaken to establish new therapeutic options for the treatment of multiple sclerosis (MS). So far, all of these strategies more or less specifically target subsets of the immune response in MS, including not only activation and expansion of T cells, their circulation and transmigration over the blood-brain barrier but also other cell types such as B cells and probably also natural killer cells. Here, we review available data on the most promising (at present) new therapeutic approaches. These involve the orally available compounds cladribine, FTY720, fumaric-acid esters, laquinimod and teriflunomide in addition to the monoclonal antibodies alemtuzumab, daclizumab, natalizumab and rituximab. After successful completion of Phase III studies, these compounds might have the potential to add to the current therapeutic armentarium especially for relapsing remitting disease courses in the near future, possibly opening the way to a more individualized treatment.

摘要

近年来,人们付出了巨大努力来建立治疗多发性硬化症(MS)的新治疗方案。到目前为止,所有这些策略或多或少都特异性地针对MS免疫反应的亚群,不仅包括T细胞的激活和扩增、它们在血脑屏障上的循环和迁移,还包括其他细胞类型,如B细胞,可能还有自然杀伤细胞。在此,我们综述了目前最有前景的新治疗方法的现有数据。这些方法除了单克隆抗体阿仑单抗、达克珠单抗、那他珠单抗和利妥昔单抗外,还包括口服可用的化合物克拉屈滨、FTY720、富马酸酯、拉喹莫德和特立氟胺。在成功完成III期研究后,这些化合物可能有潜力在不久的将来增加到当前的治疗药物库中,特别是对于复发缓解型病程,可能为更个体化的治疗开辟道路。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验