Abstract
IA2 and phogrin are important targets of humoral and cell-mediated autoimmunity in type 1 diabetes in man. They belong to a conserved subfamily of transmembrane protein tyrosine phosphatases (PTPs) associated with the regulatory pathway of secretion. To examine potential cross-reactivity between PTP family members we tested sera from T1D patients for reactivity to IA2, and the Drosophila (FLYDA) and C. elegans (IDA) orthologs using radioimmunoprecipitation assays of (35)S Met-labeled in vitro translated products of the cytosolic domains of these proteins. Approximately 80% of sera reacted with at least one probe. Of these, 82.5% showed reactivity to human IA2, 74.1% to FLYDA, and 33.7% to IDA. The majority of sera that bound FLYDA and/or IDA also recognized IA2. This raises the possibility that in some cases reactivity to IA2 may have arisen by molecular mimicry.
MeSH terms
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Animals
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Antibody Specificity
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Autoantigens / chemistry
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Autoantigens / genetics
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Autoantigens / immunology*
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Caenorhabditis elegans / enzymology
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Caenorhabditis elegans / genetics
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Case-Control Studies
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Conserved Sequence / genetics
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Conserved Sequence / immunology*
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Cross Reactions / immunology
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Diabetes Mellitus, Type 1 / immunology*
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Drosophila / enzymology
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Drosophila / genetics
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Epitope Mapping
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Epitopes / chemistry
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Epitopes / genetics
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Epitopes / immunology*
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Female
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Humans
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Male
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Multigene Family / immunology
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Multigene Family / physiology
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Protein Tyrosine Phosphatases / chemistry
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Protein Tyrosine Phosphatases / genetics
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Protein Tyrosine Phosphatases / immunology*
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Receptor-Like Protein Tyrosine Phosphatases, Class 8 / chemistry
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Receptor-Like Protein Tyrosine Phosphatases, Class 8 / genetics
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Receptor-Like Protein Tyrosine Phosphatases, Class 8 / immunology
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Sequence Homology
Substances
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Autoantigens
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Epitopes
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Protein Tyrosine Phosphatases
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Receptor-Like Protein Tyrosine Phosphatases, Class 8