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[鞘氨醇-1-磷酸信号系统与芬戈莫德治疗多发性硬化症的创新作用机制:国外文献综述]

[Sphingosine-1-phosphate signaling system and the innovative mechanism of action of fingolimod in treatment of multiple sclerosis: review of foreign literature].

作者信息

Shmyrev V I, Kryzhanovskiĭ S M, Danilycheva I V

出版信息

Zh Nevrol Psikhiatr Im S S Korsakova. 2012;112(2 Pt 2):93-7.

Abstract

Over the last years, sphingosine-1-phosphate signaling function (S1P) is thought to play a key role in the development of immunological and neurological components of multiple sclerosis (MS). Modulators of the S1P-system are highly effective in MS treatment. Fingolimod, a structural analogue of endogenous sphingosine, is a first generation drug of a new class of medications known as "modulators of sphingosine-1-phosphate receptors". The inhibition of S1P receptors by fingolimod in MS reduces the recirculation of autoreactive central memory T-cells and their infiltration of the CNS where they cause a damage that clinically reveals in the decrease in the number of MS exacerbations and less severe inflammatory brain changes in MRI.

摘要

在过去几年中,1-磷酸鞘氨醇信号传导功能(S1P)被认为在多发性硬化症(MS)的免疫和神经成分发展中起关键作用。S1P系统的调节剂在MS治疗中非常有效。芬戈莫德是内源性鞘氨醇的结构类似物,是一类被称为“1-磷酸鞘氨醇受体调节剂”的新型药物中的第一代药物。芬戈莫德在MS中对S1P受体的抑制作用减少了自身反应性中枢记忆T细胞的再循环及其向中枢神经系统的浸润,在中枢神经系统中它们会造成损害,临床上表现为MS发作次数减少以及MRI中炎症性脑改变减轻。

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