Abstract
Multiple sclerosis (MS) is the most common chronic demyelinating disease of the central nervous system (CNS) and the major cause of neurological disability in young adults in Western countries. In spite of intensive research efforts, treatment options established to date do not sufficiently prevent the accumulation of tissue damage and clinical disability in patients with MS. We here describe recently identified molecules responsible for the inflammatory and the neurodegenerative processes in MS and its animal model, experimental autoimmune encephalomyelitis (EAE), and review new treatment options targeting both aspects of this disease.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Acyl Coenzyme A / metabolism
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Animals
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Catechin / analogs & derivatives
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Catechin / therapeutic use
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Disease Models, Animal
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Encephalomyelitis, Autoimmune, Experimental
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Humans
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Multiple Sclerosis / complications*
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Multiple Sclerosis / genetics
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Multiple Sclerosis / pathology
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Nerve Degeneration / etiology*
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Nerve Degeneration / pathology
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Nerve Degeneration / prevention & control*
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Neuroprotective Agents / therapeutic use
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T-Lymphocytes / physiology
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TNF-Related Apoptosis-Inducing Ligand / metabolism
Substances
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Acyl Coenzyme A
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Neuroprotective Agents
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TNF-Related Apoptosis-Inducing Ligand
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3-hydroxy-3-methylglutaryl-coenzyme A
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Catechin
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epigallocatechin gallate