Abstract
We utilized HLA transgenic mice to identify the dominant epitopes on the human (H)-AChR alpha subunit. The cytoplasmic H-AChR peptide alpha320-337 was the dominant T cell epitope for DQ8, DR3, and DQ8xDQ6 F1 mice. The H-AChR-immunized HLA-DQ8, DR3, DQ8xDR3 F1 and DQ8xDQ6 F1 mice developed clinical EAMG, whereas HLA-DQ6 mice were less susceptible.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Cell Line
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Disease Models, Animal
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Epitope Mapping
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Epitopes / immunology
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HLA Antigens / genetics
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Humans
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Immunization / methods
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In Vitro Techniques
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Mice
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Mice, Transgenic / immunology*
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Myasthenia Gravis, Autoimmune, Experimental / chemically induced
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Myasthenia Gravis, Autoimmune, Experimental / immunology*
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Peptides / immunology
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Receptors, Cholinergic / immunology*
Substances
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Epitopes
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HLA Antigens
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Peptides
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Receptors, Cholinergic