Brain sphingosine-1-phosphate receptors: implication for FTY720 in the treatment of multiple sclerosis.
Pharmacol Ther. 2008 Jan; 117(1):77-93.P&T

Abstract

Multiple sclerosis (MS) is an autoimmune, neurological disability with unknown etiology. The current therapies available for MS work by an immunomodulatory action, preventing T-cell- and macrophage-mediated destruction of brain-resident oligodendrocytes and axonal loss. Recently, FTY720 (fingolimod) was shown to significantly reduce relapse rates in MS patients and is currently in Phase III clinical trials. This drug attenuates trafficking of harmful T cells entering the brain by regulating sphingosine-1-phosphate (S1P) receptors. Here, we outline the direct roles that S1P receptors play in the central nervous system (CNS) and discuss additional modalities by which FTY720 may provide direct neuroprotection in MS.

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Authors+Show Affiliations

Dev KK
Department of Anatomy and Neuroscience, University College Cork, Windle Building, Cork, Ireland. k.dev@ucc.ie
Mullershausen F
No affiliation info available
Mattes H
No affiliation info available
Kuhn RR
No affiliation info available
Bilbe G
No affiliation info available
Hoyer D
No affiliation info available
Mir A
No affiliation info available

MeSH

AnimalsBrainDrug Delivery SystemsFingolimod HydrochlorideHumansImmunosuppressive AgentsMultiple SclerosisPropylene GlycolsReceptors, LysosphingolipidSphingosine

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

17961662