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

被引:1087
作者
Brinkmann, Volker [1 ]
Billich, Andreas [1 ]
Baumruker, Thomas [1 ]
Heining, Peter [2 ]
Schmouder, Robert [3 ]
Francis, Gordon [4 ]
Aradhye, Shreeram [5 ]
Burtin, Pascale [6 ]
机构
[1] Novartis Inst BioMed Res, Dept Autoimmun Transplantat & Inflammat, CH-4056 Basel, Switzerland
[2] Novartis Inst BioMed Res, Dept Translat Sci, CH-4057 Basel, Switzerland
[3] Novartis Inst BioMed Res, Dept Translat Sci, Cambridge, MA 02139 USA
[4] Nova Pharmaceut Corp, Global Dev Neurosci & Ophthalm, E Hanover, NJ 07936 USA
[5] Sandoz Int GmbH, Dept Biopharma, D-83607 Holzkirchen, Germany
[6] Novartis Pharma AG, Global Dev Neurosci & Ophthalm, CH-4051 Basel, Switzerland
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; SPHINGOSINE 1-PHOSPHATE RECEPTOR; PLACEBO-CONTROLLED TRIAL; CENTRAL-NERVOUS-SYSTEM; CIRCULATING MATURE LYMPHOCYTES; SKIN ALLOGRAFT SURVIVAL; T-CELL SUBSETS; IMMUNOSUPPRESSANT FTY720; DOUBLE-BLIND; INTRAMUSCULAR INTERFERON;
D O I
10.1038/nrd3248
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
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.
引用
收藏
页码:883 / 897
页数:15
相关论文
共 157 条
[1]
DESIGN, SYNTHESIS, AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2-SUBSTITUTED-2-AMINO-1,3-PROPANEDIOLS - DISCOVERY OF A NOVEL IMMUNOSUPPRESSANT, FTY720 [J].
ADACHI, K ;
KOHARA, T ;
NAKAO, N ;
ARITA, M ;
CHIBA, K ;
MISHINA, T ;
SASAKI, S ;
FUJITA, T .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (08) :853-856
[2]
Neuronal damage in autoimmune neuroinflammation mediated by the death ligand TRAIL [J].
Aktas, O ;
Smorodchenko, A ;
Brocke, S ;
Infante-Duarte, C ;
Topphoff, US ;
Vogt, J ;
Prozorovski, T ;
Meier, S ;
Osmanova, V ;
Pohl, E ;
Bechmann, I ;
Nitsch, R ;
Zipp, F .
NEURON, 2005, 46 (03) :421-432
[3]
Novel immunomodulator FTY720 is phosphorylated in rats and humans to form a single stereoisomer.: Identification, chemical proof, and biological characterization of the biologically active species and its enantiomer [J].
Albert, R ;
Hinterding, K ;
Brinkmann, V ;
Guerini, D ;
Müller-Hartwieg, C ;
Knecht, H ;
Simeon, C ;
Streiff, M ;
Wagner, T ;
Welzenbach, K ;
Zécri, F ;
Zollinger, M ;
Cooke, N ;
Francotte, E .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (16) :5373-5377
[4]
Expression of the sphingosine 1-phosphate receptor, S1P1, on T-cells controls thymic emigration [J].
Allende, ML ;
Dreier, JL ;
Mandala, S ;
Proia, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (15) :15396-15401
[5]
G-protein-coupled receptor S1P1 acts within endothelial cells to regulate vascular maturation [J].
Allende, ML ;
Yamashita, T ;
Proia, RL .
BLOOD, 2003, 102 (10) :3665-3667
[6]
Phenotype and Function of Human T Lymphocyte Subsets: Consensus and Issues [J].
Appay, Victor ;
van Lier, Rene A. W. ;
Sallusto, Federica ;
Roederer, Mario .
CYTOMETRY PART A, 2008, 73A (11) :975-983
[7]
FTY720 sustains and restores neuronal function in the DA rat model of MOG-induced experimental autoimmune encephalomyelitis [J].
Balatoni, Balazs ;
Storch, Maria K. ;
Swoboda, Eva-M. ;
Schoenborn, Vinzenz ;
Koziel, Agnieszka ;
Lambrou, George N. ;
Hiestand, Peter C. ;
Weissert, Robert ;
Foster, Carolyn A. .
BRAIN RESEARCH BULLETIN, 2007, 74 (05) :307-316
[8]
The immune modulator FTY720 inhibits sphingosine-1-phosphate lyase activity [J].
Bandhuvula, P ;
Tam, YY ;
Oskouian, B ;
Saba, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (40) :33697-33700
[9]
Effector T cell interactions with meningeal vascular structures in nascent autoimmune CNS lesions [J].
Bartholomaeus, Ingo ;
Kawakami, Naoto ;
Odoardi, Francesca ;
Schlaeger, Christian ;
Miljkovic, Djordje ;
Ellwart, Joachim W. ;
Klinkert, Wolfgang E. F. ;
Fluegel-Koch, Cassandra ;
Issekutz, Thomas B. ;
Wekerle, Hartmut ;
Fluegel, Alexander .
NATURE, 2009, 462 (7269) :94-U104
[10]
Bartholomäus I, 2008, MULT SCLER, V14, pS30