Abstract
T lymphocytes play a pivotal role in the autoimmune response in primary biliary cirrhosis (PBC). Recent studies have shown that there is overlapping in the PDC-E2-specific T and B cell epitopes. In addition, helper T and cytotoxic T cell epitopes all contain a shared peptide sequence. In addition, recognition of exogenous antigens including bacterial antigens by autoantigen-specific T cell and the mechanism of molecular mimicry provide a clue to clarifying the pathogenesis of PBC. Furthermore, the findings that autoantigen-immune complexes cross present and also that the presentation of autoantigen is of a higher relative efficiency, define a unique role of autoantibodies in the pathogenesis of the autoimmune disease. The mechanism of immune-mediated bile duct damage in PBC, including the possible role of T cell-mediated cytotoxicity and molecular mimicry is discussed.
MeSH terms
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Animals
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Antigen Presentation
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Antigens, Bacterial / immunology
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Autoantibodies / immunology
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Autoimmunity*
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B-Lymphocytes / immunology
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Bile Ducts / pathology
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CD4-Positive T-Lymphocytes / immunology*
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Dihydrolipoyllysine-Residue Acetyltransferase
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Escherichia coli / immunology
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Humans
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Immunodominant Epitopes / chemistry
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Liver Cirrhosis, Biliary / etiology
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Liver Cirrhosis, Biliary / immunology*
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Molecular Mimicry / immunology
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Neutrophil Infiltration
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Pyruvate Dehydrogenase Complex / biosynthesis
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Pyruvate Dehydrogenase Complex / chemistry
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Pyruvate Dehydrogenase Complex / immunology
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T-Lymphocytes, Cytotoxic / chemistry
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T-Lymphocytes, Cytotoxic / immunology
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T-Lymphocytes, Helper-Inducer / chemistry
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T-Lymphocytes, Helper-Inducer / immunology
Substances
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Antigens, Bacterial
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Autoantibodies
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Immunodominant Epitopes
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Pyruvate Dehydrogenase Complex
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Dihydrolipoyllysine-Residue Acetyltransferase