Abstract
In both collagen-induced arthritis (CIA) and rheumatoid arthritis, T cells recognize a galactosylated peptide from type II collagen (CII). In this study, we demonstrate that the CII259-273 peptide, galactosylated at lysine 264, in complex with Aq molecules prevented development of CIA in mice and ameliorated chronic relapsing disease. In contrast, nonglycosylated CII259-273/Aq complexes had no such effect. CIA dependent on other MHC class II molecules (Ar/Er) was also down-regulated, indicating a bystander vaccination effect. T cells could transfer the amelioration of CIA, showing that the protection is an active process. Thus, a complex between MHC class II molecules and a posttranslationally modified peptide offers a new possibility for treatment of chronically active autoimmune inflammation such as rheumatoid arthritis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Arthritis, Experimental / chemically induced
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Arthritis, Experimental / immunology
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Arthritis, Experimental / prevention & control*
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Bystander Effect / immunology
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Cattle
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Chronic Disease
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Collagen Type II / immunology
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Collagen Type II / metabolism
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Collagen Type II / therapeutic use*
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Galactose / metabolism
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Glycosylation
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Histocompatibility Antigens Class II / immunology
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Histocompatibility Antigens Class II / metabolism
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Histocompatibility Antigens Class II / therapeutic use*
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Hybridomas / immunology
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Hybridomas / metabolism
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Immunodominant Epitopes / immunology
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Immunodominant Epitopes / metabolism
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Immunodominant Epitopes / therapeutic use
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Immunotherapy, Active*
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Lymphocyte Activation / drug effects
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Lymphocyte Activation / immunology
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Male
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Mice
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Mice, Inbred BALB C
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Multiprotein Complexes / immunology
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Multiprotein Complexes / metabolism
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Multiprotein Complexes / therapeutic use*
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Peptides / immunology
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Peptides / metabolism
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Peptides / therapeutic use*
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Rats
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Solubility
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T-Lymphocytes / drug effects
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T-Lymphocytes / immunology
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Vaccines / immunology
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Vaccines / therapeutic use*
Substances
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Collagen Type II
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Histocompatibility Antigens Class II
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Immunodominant Epitopes
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Multiprotein Complexes
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Peptides
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Vaccines
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Galactose