Central nervous system-directed effects of FTY720 (fingolimod)

被引:147
作者
Miron, Veronique E. [1 ]
Schubart, Anna [2 ]
Antel, Jack P. [1 ]
机构
[1] McGill Univ, Montreal Neurol Inst, Neuroimmunol Unit, Montreal, PQ H3A 2B4, Canada
[2] Novartis Inst Biomed Res, Basel, Switzerland
关键词
Sphingosine-1-phosphate; FTY720 (fingolimod); Multiple sclerosis; Central nervous system; Immunotherapy;
D O I
10.1016/j.jns.2008.06.031
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
FTY720, also known as fingolimod, is an orally administered sphingosine-1-phosphate (SI P) analogue that is under investigation as a therapy for both relapsing-remitting (RR) and progressive forms of multiple sclerosis (MS). The demonstrated beneficial effect of FTY720 on disease activity in RR-MS patients and in the animal model experimental autoimmune encephalomyelitis (EAE) is largely attributed to effects on the systemic immune system. In addition, unlike other Current systemic immuno-modulators used in MS, the lipophilic nature of FTY720 allows it to cross the blood-brain barrier (BBB). Since S1P receptors are expressed oil all cell types, FTY720 has the potential to exert effects directly on the BBB and on resident cells of the CNS. The latter include cells implicated in regulating immune reactivity within the CNS (astrocytes, microglia), those that are targeted by the disease process (oligodendrocytes, neurons), and those involved in repair (oligodendrocyte progenitor cells). In vitro studies document the dose-dependent effects of FTY720 on neural cell survival, differentiation, and cytoskeletal dynamics. Animal model studies, specifically EAE, indicate an overall neuroprotective effect of FTY720 mediated at least in part by its actions within the CNS. Ongoing studies will need to define the direct and indirect (via immune-modulation) effects of FTY720 on the CNS across the broad clinical spectrum of MS. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 17
页数:5
相关论文
共 71 条
[1]   Depolarisation induces rapid and transient formation of intracellular sphingosine-1-phosphate [J].
Alemany, R ;
Kleuser, B ;
Ruwisch, L ;
Danneberg, K ;
Lass, H ;
Hashemi, R ;
Spiegel, S ;
Jakobs, KH ;
Heringdorf, DMZ .
FEBS LETTERS, 2001, 509 (02) :239-244
[2]   Extracellular release of newly synthesized sphingosine-1-phosphate by cerebellar granule cells and astrocytes [J].
Anelli, V ;
Bassi, R ;
Tettamanti, G ;
Viani, P ;
Riboni, L .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (05) :1204-1215
[3]   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
[4]   Sphingosine-1-phosphate is released by cerebellar astrocytes in response to bFGF and induces astrocyte proliferation through Gi-protein-coupled receptors [J].
Bassi, R ;
Anelli, V ;
Giussani, P ;
Tettamanti, G ;
Viani, P ;
Riboni, L .
GLIA, 2006, 53 (06) :621-630
[5]   FTY720, an immunomodulatory sphingolipid mimetic: translation of a novel mechanism into clinical benefit in multiple sclerosis [J].
Baumruker, Thomas ;
Billich, Andreas ;
Brinkmann, Volker .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (03) :283-289
[6]  
Beer MS, 2000, ANN NY ACAD SCI, V905, P118
[7]   Phosphorylation of the immunomodulatory drug FTY720 by sphingosine kinases [J].
Billich, A ;
Bornancin, F ;
Dévay, P ;
Mechtcheriakova, D ;
Urtz, N ;
Baumruker, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :47408-47415
[8]  
BIONDEAU N, 2007, J NEUROCHEM, V103, P509
[9]  
Blakemore WF, 2008, CURR TOP MICROBIOL, V318, P193
[10]   The immune modulator FTY720 targets sphingosine 1-phosphate receptors [J].
Brinkmann, V ;
Davis, MD ;
Heise, CE ;
Albert, R ;
Cottens, S ;
Hof, R ;
Bruns, C ;
Prieschl, E ;
Baumruker, T ;
Hiestand, P ;
Foster, CA ;
Zollinger, M ;
Lynch, KR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :21453-21457