Abstract
Infections can trigger or exacerbate the course of Multiple Sclerosis, and both bacterial and viral agents have been implicated. These agents are recognized by host cells via pathogen-associated molecular patterns activating TLRs. We investigated the role that PAMPs play in the animal model Experimental Autoimmune Encephalomyelitis, and found various MyD88-dependent PAMPs can participate as the adjuvant to induce EAE. Studies with IRAK1-deficient mice suggest that signaling through TLRs is not required in the target organ to develop disease. This suggests that PAMPs play an important role in priming of autoreactive T cells in EAE and potentially MS.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptor Proteins, Signal Transducing / metabolism
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Adjuvants, Pharmaceutic / pharmacology*
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Animals
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Autoimmunity / drug effects*
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Cell Proliferation / drug effects
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Cells, Cultured
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Cytokines / metabolism
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Disease Models, Animal
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Dose-Response Relationship, Drug
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Drug Interactions
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Encephalomyelitis, Autoimmune, Experimental / chemically induced*
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Glycoproteins / pharmacology
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Interleukin-1 Receptor-Associated Kinases
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Intracellular Signaling Peptides and Proteins / deficiency
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Lymph Nodes / pathology
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Mice
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Mice, Inbred C57BL
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Mice, Transgenic
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Myelin-Oligodendrocyte Glycoprotein
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Myeloid Differentiation Factor 88
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Peptide Fragments / pharmacology
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Protein Serine-Threonine Kinases / deficiency
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Spleen / pathology
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Thymidine / metabolism
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Time Factors
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Toll-Like Receptors / agonists*
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Tritium / metabolism
Substances
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Adaptor Proteins, Signal Transducing
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Adjuvants, Pharmaceutic
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Cytokines
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Glycoproteins
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Intracellular Signaling Peptides and Proteins
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Myd88 protein, mouse
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Myelin-Oligodendrocyte Glycoprotein
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Myeloid Differentiation Factor 88
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Peptide Fragments
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Toll-Like Receptors
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myelin oligodendrocyte glycoprotein (35-55)
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Tritium
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Interleukin-1 Receptor-Associated Kinases
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Irak1 protein, mouse
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Protein Serine-Threonine Kinases
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Thymidine