Environmental basis of primary biliary cholangitis

被引:53
作者
Tanaka, Atsushi [1 ]
Leung, Patrick S. C. [2 ]
Gershwin, M. Eric [2 ]
机构
[1] Teikyo Univ, Sch Med, Dept Med, Tokyo 1738606, Japan
[2] Univ Calif Davis, Div Rheumatol Allergy & Clin Immunol, Sch Med, Davis, CA 95616 USA
关键词
Environment; primary biliary cholangitis; genetic background; anti-mitochondrial autoantibodies; animal models; autoimmune; PYRUVATE-DEHYDROGENASE COMPLEX; PRIMARY SCLEROSING CHOLANGITIS; HUMAN AUTOIMMUNE-DISEASES; ANTIMITOCHONDRIAL ANTIBODIES; MONOZYGOTIC TWINS; EPITHELIAL-CELLS; DNA METHYLATION; ANIMAL-MODELS; E2; SUBUNIT; BILE-ACIDS;
D O I
10.1177/1535370217748893
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Autoimmunity is a consequence of both genetic and environmental factors, occurring in genetically susceptible hosts with environmental triggers. While genome-wide association studies have revealed a number of susceptible genes contributing to etiology, the environmental triggers remain poorly understood. Primary biliary cholangitis, formally known as primary biliary cirrhosis, is considered a model autoimmune disease for which our group has extensively evaluated environmental factors involved in its etiology. Bacterial infection and xenobiotics have been proposed as candidate environmental factors that may explain tolerance breakdown and production of primary biliary cholangitis-specific antimitochondrial autoantibodies. Large-scale case-control studies have consistently detected an association of primary biliary cholangitis with urinary tract infections caused by Escherichia coli, as E. coli PDC-E2 is molecularly similar to human PDC-E2, the immunodominant target of AMAs. Another bacterium of interest is Novosphingobium aromaticivorans, a ubiquitous xenobiotic-metabolizing bacterium that produces lipoylated proteins, which are highly reactive with sera from primary biliary cholangitis patients. Regarding xenobiotics, case-control studies have suggested that frequent use of nail polish is associated with an increased susceptibility to primary biliary cholangitis. We found that 2-octynamide, the conjugate derived from 2-octynoic acid present in cosmetics, lipsticks, and some chewing gums, was unique in both its quantitative structure-activity relationship analysis and reactivity with primary biliary cholangitis sera. 2-nonyamide is another xenobiotic that also has the optimal chemical structure for xenobiotic modification of the PDC-E2 epitope, as demonstrated by the enhanced epitope recognition with AMA-positive PBC sera. Moreover, we found that C57BL/6 mice immunized with 2-octynoic acid-BSA possess many of the features characteristic to primary biliary cholangitis.
引用
收藏
页码:184 / 189
页数:6
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