Abstract
There have been significant advances in the treatment of multiple sclerosis (MS) in recent years, but further improvement in therapy is required as not all patients have responded optimally. An approach to enhancing MS treatment is to combine drugs that impact on different aspects of the disease process. We have described that the tetracycline derivative, minocycline, attenuates the severity of experimental autoimmune encephalomyelitis (EAE), a model of MS. Here, we have evaluated the combination of minocycline and glatiramer acetate (GA), a current therapy in MS, on the course of EAE in mice. This combination resulted in a significant reduction of disease severity and disease burden with attenuation of the inflammation, axonal loss and demyelination.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Analysis of Variance
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Animals
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Anti-Bacterial Agents / therapeutic use
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Cytokines / metabolism
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Demyelinating Diseases / drug therapy
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Disease Models, Animal
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Drug Synergism
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Drug Therapy, Combination
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Encephalomyelitis, Autoimmune, Experimental / chemically induced
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Encephalomyelitis, Autoimmune, Experimental / drug therapy*
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Glatiramer Acetate
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Immunosuppressive Agents / therapeutic use*
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Inflammation / drug therapy
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Lymph Nodes / cytology
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Lymph Nodes / drug effects
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Mice
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Mice, Inbred C57BL
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Minocycline / therapeutic use*
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Multiple Sclerosis / chemically induced
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Multiple Sclerosis / drug therapy
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Myelin Proteins
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Myelin-Associated Glycoprotein
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Myelin-Oligodendrocyte Glycoprotein
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Peptides / therapeutic use*
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Silver Staining / methods
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Spleen / cytology
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Spleen / drug effects
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Time Factors
Substances
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Anti-Bacterial Agents
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Cytokines
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Immunosuppressive Agents
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Mog protein, mouse
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Myelin Proteins
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Myelin-Associated Glycoprotein
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Myelin-Oligodendrocyte Glycoprotein
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Peptides
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Glatiramer Acetate
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Minocycline