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FTY720 on the way from the base camp to the summit of the mountain: relevance for remyelination

Journal

MULTIPLE SCLEROSIS JOURNAL
Volume 18, Issue 3, Pages 258-263

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1352458512438723

Keywords

multiple sclerosis; fingolimod; FTY720; remyelination; neuroprotection; cuprizone; toxic demyelination

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FTY720 (fingolimod; Gilenya (R)), a sphingosine I-phosphate (SIP) receptor modulator, is the first oral disease-modifying therapy to be approved for the treatment of relapsing-remitting multiple sclerosis. FTY720 is rapidly converted in vivo to the active S-fingolimod-phosphate, which binds to SIP receptors. This action inhibits egress of lymphocytes from the lymph nodes, preventing entry into the blood and thus infiltration into the central nervous system. More recent studies, however, convincingly show that FTY720 crosses the blood-brain barrier, where it is thought to act on SIP receptors on cells within the central nervous system, such as astrocytes, oligodendrocytes or microglia. Here we discuss the evidence showing that FTY720 also plays a role in remyelination and repair within the brain. While the mechanisms of action still require firm elucidation, it is clear that FTY720 could also be reparative, extending its therapeutic potential for multiple sclerosis.

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