| Literature DB >> 20625066 |
Olaf Stüve1, Bernd C Kieseier, Bernhard Hemmer, Hans-Peter Hartung, Amer Awad, Elliot M Frohman, Benjamin M Greenberg, Michael K Racke, Scott S Zamvil, J Theodore Phillips, Ralf Gold, Andrew Chan, Uwe Zettl, Ron Milo, Ellen Marder, Omar Khan, Todd N Eagar.
Abstract
Over the past 2 decades, enormous progress has been made with regard to pharmacotherapies for patients with multiple sclerosis. There is perhaps no other subspecialty in neurology in which more agents have been approved that substantially alter the clinical course of a disabling disorder. Many of the pharmaceuticals that are currently approved, in clinical trials, or in preclinical development were initially evaluated in an animal model of multiple sclerosis, experimental autoimmune encephalomyelitis. Two Food and Drug Administration-approved agents (glatiramer acetate and natalizumab) were developed using the experimental autoimmune encephalomyelitis model. This model has served clinician-scientists for many decades to enable understanding the inflammatory cascade that underlies clinical disease activity and disease surrogate markers detected in patients.Entities:
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Year: 2010 PMID: 20625066 PMCID: PMC3670826 DOI: 10.1001/archneurol.2010.158
Source DB: PubMed Journal: Arch Neurol ISSN: 0003-9942