期刊文献+

白细胞介素10基因启动子区多态性与乙型肝炎病毒感染预后的关联研究 被引量:12

Associated study on interleukin 10 gene promoter polymorphisms related to hepatitis B virus infection in Chinese Han population
原文传递
导出
摘要 目的探讨中国汉族人白细胞介素10基因(interleukin10gene,IL10)启动子区单核苷酸多态性与乙型肝炎病毒(hepatitisBvirus,HBV)感染、转归的关联。方法采用聚合酶链反应-限制性片段长度多态性分析方法,检测231例HBV感染者,165例HBV感染康复者和135名正常对照者IL10基因启动子-1082G/A、-819T/C、-592A/C位点基因型。结果IL10基因启动子-1082G/A、-819T/C、-592A/C位点基因型和等位基因在HBV感染组、HBV感染康复组和正常对照组之间的分布频率比较差异无统计学意义(P>0.05),在血清HBV-DNA<1×103拷贝/mL的HBV感染者组和HBV-DNA≥1×103拷贝/mL组之间的分布频率比较差异亦无统计学意义(P>0.05);但IL10基因启动子-819T/C和-592A/C位点基因型和等位基因在HBV无症状携带组和慢性乙型肝炎组之间的分布差异有统计学意义(P<0.05),-819T/C位点TT型和-592A/C位点AA型在慢性乙型肝炎组的频率明显较高。结论汉族人IL10基因启动子多态性可能与人群对HBV易感性及感染后的病毒血症水平无显著相关性;但IL10启动子-819T/C和-592A/C位点基因多态性与HBV感染后的肝脏炎症反应有关。 Objective To investigate the association that the polymorphisms of intedeukin 10 gene (IL10) promoter region are related to the susceptibility and clinical phenotypes of hepatitis B vires(HBV) in Chinese Han population. Methods With polymerase chain reaction with restriction fragment length polymorphism(PCR-RFLP)methed, the single nucleotide polymorphisms(SNP)of the promoter region of IL10 gene at position - 1082G/A, - 819T/C, - 592A/ C were detected in 231 patients with chronic hepatitis B, 165 individuals spontaneously recovered from HBV infection and 135 normal controls. Results No significant difference was found in frequencies of genotypes and alleles of IL10 gene promoter region at position - 1082G/A, - 819T/C, - 592A/C among normal controls, individuals spontaneously recovering from HBV infection and patients with chronic hepatitis B ( P 〉 0.05 ), also between patients with HBV infection with HBV-DNA 〈 1 × 10^3 copies/mL and those with HBV-DNA≥ 1 ×10^3 copies/mL( P 〉 0.05). However, frequencies of TT genotype at position - 819T/C and AA genotype at position - 592A/C in chronic hepatitis B were significantly higher than that in asymptomatic HBV carriers( P 〈 0.05). Conclusion It is possible that genetic polymorphisms of 11,10 promoter region are not associated with both susceptibility of HBV infection and HBV-DNA replication after infected HBV in Chinese Hart population. However, the polymorphisms of the promoter region ofIL10 at position - 819T/C and - 592A/C are related to inflammatory reaction to liver of the patients with HBV infection.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2006年第4期410-414,共5页 Chinese Journal of Medical Genetics
关键词 白细胞介素10 基因多态性 乙型肝炎病毒 interleukin 10 gene polymorphism hepatitis B virus
作者简介 Email : Zhangpingan@ yahoo, com. cn
  • 相关文献

参考文献3

二级参考文献64

  • 1Liang-PingLu,Xing-WangLi,YingLiu,Guo-ChangSun,Xue-PingWang,Xi-LinZhu,Quan-YouHu,HuiLi.Association of -238G/A polymorphism of tumor necrosis factor-alpha gene promoter region with outcomes of hepatitis B virus infection in Chinese Han population[J].World Journal of Gastroenterology,2004,10(12):1810-1814. 被引量:19
  • 2[43]Griffiths PD. Interactions between viral and human genes. Rev Med Virol 2002; 12:197-199
  • 3[44]Dean M, Carrington M, O′Brien SJ. Balanced polymorphism selected by genetic versus infectious human disease. Annu Rev Genomics Hum Genet 2002; 3:263-292
  • 4[1]Gu CH, Luo KX. Hepatitis B: Basic biology and clinical science. Second edition. Beijing, People′s Medical Publishing House 2001:1-6
  • 5[2]Iino S. Natural history of hepatitis B and C virus infections. Oncology 2002; 62(Suppl 1): 18-23
  • 6[3]Luo KX. Hepatitis B: Basic biology and clinical science. Second edition. Beijing, People′s Medical Publishing House 2001:56-70
  • 7[4]Ferrari C. Hepatitis B virus immunopathogenesis. Annu Rev Immunol 1995; 13:29-60
  • 8[5]Guidotti LG, Chisari FV. Noncytolytic control of viral infections by the innate and adaptive immune response. Annu Rev Immunol 2001; 19:65-91
  • 9[6]Abel L, Dessein AJ. The impact of host genetics on susceptibility to human infectious diseases. Curr Opin Immunol 1997; 9:509-516
  • 10[7]McNicholl J. Host genes and infectious diseases. Emerg Infect Dis 1998; 4:423-426

共引文献125

同被引文献122

引证文献12

二级引证文献31

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