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Volume 355:1088-1091 September 14, 2006 Number 11
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Fingolimod and Sphingosine-1-Phosphate — Modifiers of Lymphocyte Migration
Steffen Massberg, M.D., Ph.D., and Ulrich H. von Andrian, M.D., Ph.D.

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Multiple sclerosis is considered an autoimmune disease in which CD4+ T cells and macrophages destroy oligodendrocytes, which synthesize and maintain axonal myelin sheaths in the central nervous system (CNS). This misguided attack results in progressive focal demyelination that can cause severe neurologic disability. In this issue of the Journal, Kappos et al. (pages 1124–1140) report that the immunosuppressant fingolimod (also called FTY720 or 2-amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol hydrochloride) exerted considerable therapeutic effects in a small, placebo-controlled clinical trial involving patients with relapsing multiple sclerosis. Patients who received oral fingolimod once daily had a rapid reduction in disease activity, reflected in significant reductions in . . . [Full Text of this Article]


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Dr. Massberg is a research fellow in pathology at Harvard Medical School and at the CBR Institute for Biomedical Research, Boston. Dr. von Andrian is a senior investigator at the CBR Institute for Biomedical Research and a professor of pathology at Harvard Medical School, Boston.


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