期刊文献+

CD68在慢性乙型肝炎发病机制的临床初步研究 被引量:3

Preliminary clinical study of CD68 in the pathogenesis of chronic hepatitis B
下载PDF
导出
摘要 目的分析健康人群和慢性乙型肝炎(CHB)患者CD68表达情况,研究CD68表达与乙型肝炎病毒(HBV)血清学、肝功能等相关性。方法分析血清、外周血单个核细胞(PBMC)CD68含量及mRNA表达水平;采用免疫组化染色技术分析PBMC与肝组织CD68表达情况;运用实时荧光定量PCR检测患者外周血病毒载量及其基因分型。分别以t检验和Pearson相关性检验分析CD68在CHB患者与健康对照血清中差异及其与其它指标相关性。结果与健康对照组比较,CHB组血清CD68含量显著升高,且与HBV DNA载量、ALT、AST水平呈显著正相关性(r=0.355 0,P=0.0014;r=0.345 0,P=0.002 0;r=0.328 9,P=0.003 3),而与乙肝表面抗原(HBsAg)含量、HBV基因分型及乙肝e抗原(HBeAg)状态无相关性(r=0.085,P=0.459;t=1.251,P=0.215;t=1.293,P=0.200)。CD68在CHB组和健康对照组PBMC中mRNA和蛋白表达水平差异无统计学意义,但CHB组肝组织CD68含量显著高于健康对照组。结论 CHB患者CD68与病毒复制及肝细胞损伤密切相关,且在肝组织呈现较高表达,提示CD68在慢性乙型肝炎发病机制中可能具有重要作用。 Objective To investigate the levels of CD68 in healthy controls and patients with chronic hepatitis B(CHB),and analyze whether it is associated with HBV markers as well as liver function indexes. Methods The levels of CD68 in serum and peripheral blood mononuclear cell( PBMC) were analyzed. Both the expression of CD68 in PBMC and hepatic tissue specimens were used to analyze by immunohistochemical( IHC) methods. Moreover,HBV DNA load and HBV genotype were detected by Real-Time PCR. The serum and PBMC levels of CD68,liver function indexes in patients with CHB and healthy controls were compared by t test. Meanwhile,the association between CD68 with HBV markers and liver function indexes were analysed using by Pearson correlation test.Results Compared with healthy controls,serum CD68 levels in patients with CHB were significantly increased,and positively correlated with HBV DNA load,ALT and AST,respectively( r = 0. 355 0,P = 0. 001 4;r = 0. 345 0,P = 0. 002 0;r = 0. 328 9,P = 0. 003 3). In contrast,there was no correlation between CD68 with hepatitis B surface antigen( HBs Ag) quantification,HBV genotype and hepatitis B e antigen( HBe Ag) status( r = 0. 085,P =0. 459;t = 1. 251,P = 0. 215;t = 1. 293,P = 0. 200). There was no significant difference of CD68 in PBMC between CHB patients and healthy controls. However,the expression of CD68 in liver specimens of CHB patients was markedly higher than that in healthy controls. Conclusion The CD68 concentrations closely relate to HBV replication and liver injury in patients with CHB,especially high expression in liver of CHB patients,suggesting that it might plays an important roles of pathogenesis in CHB patients.
作者 陈治东 管世鹤 杨凯 张浩 姚杰 程婉秋 Chen Zhidong;Guan Shihe;Yang Kai(Dept of Laboratory,The Second Affiliated Hospital of Anhui Medical University,Hefei 230601)
出处 《安徽医科大学学报》 CAS 北大核心 2018年第8期1271-1275,共5页 Acta Universitatis Medicinalis Anhui
基金 安徽省卫生计生委科研计划项目(全科医学临床科研课题)(编号:2016QK014) 安徽省教育厅高等学校省级质量工程项目(编号:2016jxtd059)
关键词 CD68 慢性乙型肝炎 乙型肝炎病毒 CD68 chronic hepatitis B HBV
  • 相关文献

参考文献2

二级参考文献15

  • 1E1-Serag HB. Epidemiology of viral hepatitis and hepatocellular carcinoma. Gastroenterology, 2012, 142:1264-1273 e1.
  • 2Kolls JK, Linden A. Interleukin-17 family members and inflammation. Immunity, 2004, 21: 467-476.
  • 3Leipe J, Grunke M, Dechant C, et al. Role of Thl7 cells in human autoimmune arthritis. Arthritis Rheum, 2010, 62 : 2876-2885.
  • 4Miossec P, Kolls JK. Targeting IL-17 and TH17 cells in chronic inflammation. Nat Rev Drug Discov, 2012, 11:763- 776.
  • 5Liaw YF, Chu CM. Hepatitis 12, virus infection. Lancet, 2009, 373 .. 582-592.
  • 6Bertoletti A, Ferrari C. Innate and adaptive immune responses in chronic hepatitis B virus infections: towards restoration of immune control of viral infection. Postgrad Med J, 2013, 89.. 294-304.
  • 7Mndri M, Locarnini S. New insight in the pathobiology of hepatitis B virus infection. Gut, 2012, 61: i6-i17.
  • 8Busca A, Kumar A. Innate immune responses in hepatitis B virus (HBV) infection. Virol J, 2014, 11: 22.
  • 9Bilzer M, Roggel F, Gerbes AL. Role of Kupffer cells in host defense and liver disease. Liver Int, 2006, 26; 1175-1186.
  • 10Stienstra R, Saudale F, Duval C, et al. Kupffer cells promote hepatic steatosis via interleukin lbeta-dependent suppression of peroxisome proliferator-activated receptor alpha activity. Hepatology, 2010, 51: 511-522.

共引文献617

同被引文献25

引证文献3

二级引证文献9

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