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慢性丙型肝炎患者肝免疫标志物和病毒基因型研究 被引量:2

Correlation between hepatic immunological markers and virus genotype in patients with chronic hepatitis C
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摘要 目的研究慢性丙型肝炎患者肝免疫标志物和病毒基因型的关系。方法取28例HFE基因型患者的肝活检标本进行切片染色,并通过形态测定法分析CD8,主要组织相容性复合体-Ⅰ类(majorhistocompatibilitycomplexclassⅠ,MHC-Ⅰ),β2微球蛋白(β2microglobulin,β2-mG),HFE和CD68。其中18例患者的治疗应答性资料有效。结果CD8+常聚集于肝汇管区和窦状隙,CD8+与MHC-Ⅰ阳性内样细胞相互作用。MHC-Ⅰ和β2-mG主要表达于内皮细胞和枯否细胞,而大多数HFE表达于圆形和树突状CD68+细胞。基因型为3a的丙型肝炎患者肝MHC-Ⅰ和HFE强表达,且对干扰素治疗持续应答率较高。结论慢性丙型肝炎患者MHC-Ⅰ的肝脏表达可能与病毒基因型相关。HCV3a基因型上调MHC-Ⅰ和HFE的表达。 Objective To investigate the hepatic expression of immunological markers relevant to a eytotoxic response in relation to viral genotype. Methods The frozen liver biopsies were obtained from 28 HFE genotyped patients and made the sections stained. The morphometry was used to analyze the major histocompatibility complex class Ⅰ(MHC- Ⅰ), CD8^+β2-mieroglobulin (β2- mG), HFE and CD68 in the stained sections. Biopsy data of response to therapy with interferon were available in 18 eases. Results CD8 ^+ was usually clustered together and localized in portal tracts and sinusoids, and seen to interact with MHC- Ⅰ positive lining cells. MHC- Ⅰand β2- mG were expressed mainly in endothelial and Kupffer cells, lIFE was expressed in most round and dendritic CD68 ccells. Patients with virus genotype 3a had higher hepatic MHC- Ⅰand HFE expression, and a better sustained response to interferon (IFN) therapy than patients without. Conclusion The MHC- Ⅰ expression in the liver of patient with chronic hepatitis C virus infection seems to relate to viral-genotype. The hepatic MHC-Ⅰ and HFE expression are higher in patients with virus genotype 3a than that in patients with non-3a genotype.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2006年第4期452-455,共4页 Chinese Journal of Medical Genetics
关键词 丙型肝炎病毒 主要组织相容性复体-Ⅰ类 干扰素 hepatitis C virus major histocompatibility complex class Ⅰ interferon
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参考文献18

  • 1Global surveillance and control of hepatic C.Report of a WHO consultation organized in collaboration with the viral hepatitis prevention board,Antwerp,Belgium.J Viral Hepat,1999,6:35-47.
  • 2Bonkovsky HL.Iron as a comorbid factor in chronic viral hepatitis.Am J Gastroenterol,2002,97:1-4.
  • 3Freeman AJ,Pan Y,Harvey CE,et al.The presence of an intrahepatic cytotoxic T lymphocyte response is associated with low viral load in patients with chronic hepatitis C virus infection.J Hepatol,2003,38:349-356.
  • 4Sreenarasimhaiah J,Jaramillo A,Crippin J,et al.Lack of optimal T-cell reactivity against the hepatitis C virus is associated with the development of fibrosis/cirrhosis during chronic hepatitis.Hum Immunol,2003,64:224-230.
  • 5彭文伟 李刚.病毒性肝炎[A].见:彭文卫 李兰娟 乔光彦 主编.传染病学第6版[C].北京:人民卫生出版社,2004.21-50.
  • 6Cardoso CS,Alves H,Mascarenhas M,et al.Co-selection of the H63D mutation and the HLA-A29 allele:a new paradigm of linkage disequilibrium? Immunogenetics,2002,53:1002-1008.
  • 7田伟,罗奇志,李立新,金和坤,王帆,郭实士,曹亚.湖南地区鼻咽癌MHC-Ⅰ类链相关基因A第5外显子微卫星多态性研究[J].中华医学遗传学杂志,2005,22(3):309-312. 被引量:4
  • 8Burgio VL,Ballardini G,Artini M,et al.Expression of co-stimulatory molecules by Kupffer cells in chronic hepatitis C virus etiology.Hepatology,1998,27:1600-1606.
  • 9Liang TJ,Rehermann B,Seeff LB,et al.Pathogenesis,natural history,treatment,and prevention of hepatitis C.Ann Intern Med,2000,132:296-305.
  • 10Barbaro G,Di Lorenzo G,Ribersani M,et al.Serum ferritin and hepatic glutathione concentrations in chronic hepatitis C patients related to the hepatitis C virus genotype.J Hepatol,1999,30:774-782.

二级参考文献17

  • 1Bahrain S, Bresnahan M, C, eraghty DE, et al. A second lineage of mam-malian major histocompatibility complex class I genes. Proc Nail Acad Sci U S A, 1994,91:6259-6263.
  • 2Groh V, Bahram S, Bauer S, et al. Cell stress-regulated human major histocompatibility complex class I gene expressed in gastrointestinal epithelium. Proc Nail Aead Sci U S A, 1996,93: 12445-12450.
  • 3Groh V, Rhinehart R, Secrist H, et al. Broad tumor-associated expressionand recognition by tumorderived gamma delta T ceils of MICA and MICB.Proc Nail Acad Sei U S A, 1999,96:6879-.6884.
  • 4Bauer S, Groh V, Wu J, et al. Activation of NK cells and T cells by NKG2D, a receptor for stress-inducible MICA. Science, 1999,285 : 727-729.
  • 5Girardi M, Oppenheim DE, Steele CR, et al. Regulation of cutaneous malignancy by gammadelta T cells. Science,2001,294:605-609.
  • 6Mizuki N, Ota M, Kimura M,et al.Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association d six GCT repetitions with Behcet disease. Proc Nail Acad Sci U S A, 1997,94:1298-1303.
  • 7Tian W, Boggs DA, Ding WZ, et al. MICA genetic polymorphism and linkage disequilibrium with HLA-B in 29 African-American families. Immunogenetics, 2001,53 : 724-728.
  • 8Collins RW, Stephens HA, Clare MA, et al.High resolution molecular phototyping of MICA and MICB alleles using sequence specific primers.Hum Immunol, 2002,63 : 783-794.
  • 9La SJ,Day NE, Degm L, et al. Linkage of a nasohparyngeal carcinoma susceptibility locus to the HI.,A region. Nature, 1990,346:470M71.
  • 10Ooi EE, Ren EC, Chan SH. Association between micrasatellites within the human MHC and nasopharyngeal carcinoma. Int J Cancer, 1997,74:229-232.

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