芬戈莫德(FTY720):一种治疗多发性硬化症的口服药物的发现和开发。

Fingolimod (FTY720): discovery and development of an oral drug to treat multiple sclerosis.

机构信息

Department of Autoimmunity, Transplantation and Inflammation, Novartis Institutes for BioMedical Research, Novartis Campus Forum 1, WSJ-386, CH-4056 Basel, Switzerland.

出版信息

Nat Rev Drug Discov. 2010 Nov;9(11):883-97. doi: 10.1038/nrd3248. Epub 2010 Oct 29.

Abstract

The discovery of fingolimod (FTY720/Gilenya; Novartis), an orally active immunomodulatory drug, has opened up new approaches to the treatment of multiple sclerosis, the most common inflammatory disorder of the central nervous system. Elucidation of the effects of fingolimod--mediated by the modulation of sphingosine 1-phosphate (S1P) receptors--has indicated that its therapeutic activity could be due to regulation of the migration of selected lymphocyte subsets into the central nervous system and direct effects on neural cells, particularly astrocytes. An improved understanding of the biology of S1P receptors has also been gained. This article describes the discovery and development of fingolimod, which was approved by the US Food and Drug Administration in September 2010 as a first-line treatment for relapsing forms of multiple sclerosis, thereby becoming the first oral disease-modifying therapy to be approved for multiple sclerosis in the United States.

摘要

芬戈莫德(FTY720/Gilenya;诺华)的发现为多发性硬化症的治疗开辟了新途径,多发性硬化症是中枢神经系统最常见的炎症性疾病。芬戈莫德通过调节鞘氨醇 1-磷酸(S1P)受体的作用机制已经阐明,其治疗活性可能是由于调节选定的淋巴细胞亚群向中枢神经系统的迁移和对神经细胞(特别是星形胶质细胞)的直接作用。对 S1P 受体生物学的理解也得到了提高。本文描述了芬戈莫德的发现和开发,该药于 2010 年 9 月获得美国食品和药物管理局批准,作为治疗复发型多发性硬化症的一线药物,成为美国批准的首个用于多发性硬化症的口服疾病修正治疗药物。

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