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用于复发型多发性硬化症的FTY720(芬戈莫德)

FTY720 (fingolimod) for relapsing multiple sclerosis.

作者信息

Horga Alejandro, Montalban Xavier

机构信息

Clinical Neuroinmunology Unit, Multiple Sclerosis Center of Catalonia (CEM-Cat), Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

Expert Rev Neurother. 2008 May;8(5):699-714. doi: 10.1586/14737175.8.5.699.

Abstract

FTY720 (fingolimod) is a structural analogue of sphingosine, an endogenous lysophospholipid, which targets sphingosine-1-phosphate receptors after biotransformation to FTY720-phosphate. The immunomodulatory properties of this agent are mainly related to its ability to entrap lymphocytes in secondary lymphoid organs, reducing their availability for cell-mediated immune responses. Emerging evidence suggests that FTY720 also exerts direct actions on glial and precursor cells of the CNS which may be relevant for the process of tissue repair after injury. The therapeutic effects of the drug observed in animal models of human multiple sclerosis have provided the experimental basis for its clinical application. A recent Phase II study has demonstrated that oral FTY720 is effective in reducing disease activity in relapsing multiple sclerosis with a favorable adverse-effect profile. These results are awaiting confirmation in the three ongoing Phase III clinical trials evaluating FTY720 for relapsing-remitting multiple sclerosis.

摘要

FTY720(芬戈莫德)是鞘氨醇(一种内源性溶血磷脂)的结构类似物,它在生物转化为磷酸FTY720后作用于1 - 磷酸鞘氨醇受体。该药物的免疫调节特性主要与其将淋巴细胞截留在二级淋巴器官中的能力有关,从而减少其参与细胞介导免疫反应的可能性。新出现的证据表明,FTY720对中枢神经系统的神经胶质细胞和前体细胞也有直接作用,这可能与损伤后组织修复过程相关。在人类多发性硬化症动物模型中观察到的该药物治疗效果为其临床应用提供了实验依据。最近的一项II期研究表明,口服FTY720可有效降低复发型多发性硬化症的疾病活动度,且不良反应较少。这些结果有待正在进行的三项评估FTY720治疗复发缓解型多发性硬化症的III期临床试验予以证实。

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