期刊文献+

原发性胆汁性肝硬化基因易感性的研究进展 被引量:1

Research Advance on Genetic Susceptibility of Primary Biliary Cirrhosis
原文传递
导出
摘要 原发性胆汁性肝硬化(PBC)是一种由自身免疫机制介导的慢性进行性胆汁淤积性肝脏疾病。近年来,其发病率逐年增长,研究表明谷胱甘肽S转换酶(GST)、细胞毒性T淋巴细胞相关抗原4(CTLA-4)、血管内皮细胞一氧化氮合成酶(eNOS)、人类白细胞分化抗原(HLA)、IL-10、细胞角蛋白19(CK19)、甘露糖结合凝集素(MBL)、IL-1、TNF-α基因以及x染色体关联的基因等可能与PBC相关。我对与PBC易感性相关的基因的研究进展进行综述,为今后的研究提供一定的依据。 The incidence of primary biliary cirrhosis (PBC), a chronic progressive cholestetic liver disease caused by autoimmune mechanism, is increasing these years. Recent studies showed that genes encoded glutathione S-transferase (GST), cytotoxic T lymphocyte associated antigen-4( CTLA-4), endothelial nitric ox- ide synthase (eNOS), human leucocyte antigen, interleukin-10 (IL-10), cytokeratinl9 (CK19), mannosebinding lectin ( MBL), interleukin-1 ( IL-1 ), tumor necrosisfactor-alpha (TNF-α), and X chromosome linked genes, might be related to the susceptibility of PBC. Here we reviewed the latest literatures for further investigation.
出处 《国际免疫学杂志》 CAS 2007年第2期84-87,共4页 International Journal of Immunology
基金 国家自然科学基金资助项目(30471616) 上海市重点基础研究项目(05JC14052)
关键词 原发性胆汁性肝硬化 自身免疫 基因 易感性 Primary biliary cirrhosis Autoimmune Gene Susceptibility
  • 相关文献

参考文献1

二级参考文献19

  • 1Czaja AJ, Strettell MD, Thomson LJ, et al.Associations between alleles of the major histocompatibility complex and type 1 autoimmune hepatitis. Hepatology, 1997,25:317-323.
  • 2Qiu DK, Ma X. Relationship between human leukocyte antigenDRB1 and autoimmune hepatitis type Ⅰ in Chinese patients. J Gastroenterol Hepatol,2003, 18:63-67.
  • 3Donaldson P, Agarwal K, Craggs A, et al. HLA and interleukin 1 gene polymorphisms in primary biliary cirrhosis: associations with disease progression and disease susceptibility. Gut, 2001, 48:397-402.
  • 4Vogel A, Strassburg CP, Manns MP. Genetic association of vitamin D receptor polymorphisms with primary biliary cirrhosis and autoimmune hepatitis. Hepatology, 2002,35:126-131.
  • 5Vaidya B, Imrie H, Perros P, et al. The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus. Hum Mol Genet, 1999,8:1195-1199.
  • 6Nistico L, Buzzetti R, Pritchard LE, et al. The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with type I diabetes. Hum Mol Genet, 1996,5:1075-1080.
  • 7Gonzalez-Escribano MF, Rodriguez R, Valenzuela A, et al. CTLA-4 polymorphisms in Spanish patients with rheumatoid arthritis. Tissue Antigens, 1999,53:296-300.
  • 8Lee YH, Choi SJ, Ji JD, et al. No association of polymorphisms of the CTLA-4 exon 1(+49) and promoter (-318) genes with rheumatoid arthritis in the Korean population. Scand J Rheumatol, 2002,31:266-270.
  • 9Bocko D, Bilinska M, Dobosz T, et al. Lack of association between an exon 1 CTLA-4 gene polymorphism A(49)G and multiple sclerosis in a Polish population of the Lower Silesia region. Arch Immunol Ther Exp (Warsz), 2003,51:201-205.
  • 10Kantarci OH, Hebrink DD, Achenbach SJ, et al. CTLA-4 is associated with susceptibility to multiple sclerosis. J Neuroimmunol, 2003,134:133-141.

共引文献7

同被引文献6

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部