The immune response to mitochondrial autoantigens

被引:30
作者
Ishibashi, H [1 ]
Shimoda, S
Gershwin, ME
机构
[1] Natl Hosp Org, Nagasaki Med Ctr, Clin Res Ctr, Nagasaki 8568562, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Med Ctr, NHO,Gen Clin Res Ctr,Dept Hepatol, Nagasaki 852, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Fukuoka 812, Japan
[4] Univ Calif Davis, Div Rheumatol Allergy & Clin Immunol, Genome & Biomed Sci Facil, Davis, CA 95616 USA
关键词
anti mitochondrial antigen; 2-oxo-acid dehydrogenase complex; biliary epithelial cell; CD4(+) helper T cell; molecular mimicry;
D O I
10.1055/s-2005-916325
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Similar to other autoimmune diseases, there are intense humoral and cellular responses to intracytoplasmic antigens in primary biliary cirrhosis (PBC). The autoantigens against antimitochondrial antibodies (AMAs) in PBC are located on the inner mitochondrial membrane and are identified as members of the 2-oxo-acid dehydrogenase complexes (2-OADCs), of which the E2 subunit of pyruvate dehydrogenase complex (PDC-E2) is the major autoantigen; AMAs are present in approximately 90 to 95% of PBC sera. An orchestrated immune response against the intrahepatic billary epithelial cell (BEC) through 2-OADC-specific CD4(+) helper T cells and CD8(+) CTL are thought to be the major players in the immunological destruction of BECs in PBC. We believe that a prior/ primary event of specific intrahepatic BEC malfunction (possibly caused by environmental insults such as xenobiotics and microorganisms) is responsible for the breaking of self tolerance to 2-OADC and leads to BEC destruction. The generation of 2-OADC-specific T cells further accelerates the damage of BEC. In addition, immunoglobulin A AMAs may participate in the destruction of BECs by damaging mitochondria.
引用
收藏
页码:337 / 346
页数:10
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