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|a 10.1016/j.clim.2011.10.008
|2 doi
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|a eng
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| 100 |
1 |
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|a Ingwersen, Jens
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Fingolimod in multiple sclerosis
|b mechanisms of action and clinical efficacy
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|c 2012
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|a Text
|b txt
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|a ƒaComputermedien
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|a Date Completed 06.03.2012
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|a Date Revised 19.11.2015
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2011 Elsevier Inc. All rights reserved.
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|a Fingolimod, also known as FTY720, has recently been approved by the regulatory authorities in the US, EU, Australia, Russia, among others, for the treatment of relapsing-remitting multiple sclerosis. Fingolimod therefore represents the first oral drug for the treatment of this autoimmune disease of the central nervous system. Fingolimod modulates sphingosine-1 phosphate receptors and has unique immunoregulatory properties. Mechanistic studies from animal models have shown that fingolimod prevents immune cells from exiting from the lymphoid tissue and reaching the inflammatory tissue. Indeed, two phase III studies that laid the basis for fingolimod's approval demonstrated that fingolimod efficiently improves the relapse rate compared to both placebo and one of the standard MS medications. In this review, we will summarize the immunological profile of fingolimod, discuss the possible direct neurobiological effects that have been suggested recently and present the clinical data regarding the efficacy and safety profiles of this promising new drug
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Review
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|a Immunosuppressive Agents
|2 NLM
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|a Propylene Glycols
|2 NLM
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|a Fingolimod Hydrochloride
|2 NLM
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|a G926EC510T
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|a Sphingosine
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|a Kuery, Patrick
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|a Kieseier, Bernd
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|a Boyko, Alexey
|e verfasserin
|4 aut
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| 700 |
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|a Hartung, Hans-Peter
|e verfasserin
|4 aut
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|t Clinical immunology (Orlando, Fla.)
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