期刊文献+

慢性乙型肝炎患者外周血细胞因子诱导的杀伤细胞的动态观察 被引量:5

Dynamic observation of cytokine-induced killer cells in peripheral blood from pa- tients with chronic hepatitis B
原文传递
导出
摘要 目的:动态观察慢性乙型肝炎患者细胞因子诱导的杀伤(CIK)细胞的增殖及杀伤活性。方法:抽取10例健康人及20例慢性乙型肝炎患者的外周血,常规分离单个核细胞(PB-MC),加IFN-γ、IL-2及抗人CD3单克隆抗体(mAb)后培养,诱导CIK细胞形成。于培养后3、6、12、24及30 d,取培养的 细胞,用流式细胞仪检测CIK细胞表面CD3、CD4和CD8以及CD4、CD25、CD3、CD56和CD95、CD28分子的表达水平、增殖及杀伤活性。结果:慢性乙型肝炎患者CIK细胞的增殖及杀伤活性均低于正常对照组。培养不同时间乙肝患者CIK细胞的增殖倍数、杀伤活性和上述表面标志的表达水平,均较培养前明显增高,于培养后12 d达高峰。结论:慢性乙型肝炎患者CIK细胞的增殖倍数、杀伤活性均低于正常人,但明显高于培养前;这可能是导致HBV感染持续发展的原因之一。 AIM: To oberve dynamically proliferation and cytotoxicity of cy-tokine-induced killer cells (CIKs) in peripheral blood from patients with persistent infection of hepatitis B virus. METHODS: Peripheral blood mononuclear cells (PBMCs) were isolated routinely from 10 normal volunteers (control group) and 20 patients with chronic hepatitis B. PBMCs were co-cultured with IFN-γ, rhlL-2 and anti-CD3 mAb to induce CIK cell generation. The expressions of single staining CD3, CD4, and CD8, as well as double staining CD4 CD25, CD3 CD56 and CD28 CD95 on CIK cells were analyzed by flow cytomctry on 3,6,12,24 and 30 days of co-culture. RESULTS: The prolif-erative level and killer activity of CIK cells from the patients were lower than those from control group. The proliferative multiple, killer activity and expressions of above surface markers on CIK cells from the patients at various times after co-culture were higher than those before co-culture, and reached peak values on 12 days after co-culture. CONCLUSION: The proliferative multiple and killer activity of CIK cells from the patients are lower than that of normal people, which may be the reason of persistent development of HBV infection.
作者 黄俭 陈作严
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2003年第6期554-556,共3页 Chinese Journal of Cellular and Molecular Immunology
关键词 乙型肝炎病毒 细胞因子诱导的杀伤 增殖 细胞毒作用 hepatitis B virus cytokine-induced killer cell proliferation cytotoxicty
  • 相关文献

参考文献3

二级参考文献11

  • 1Sakaguchi S.Immunologic tolerance maintained by CD25+ CD4+regulatory T cells: their common role in controlling autoimmunity,tumor immunity and transplantation tolerance[].Immunological Reviews.2001
  • 2Shimizu J,Yamazaki S,Takahashi T,et al.Stimulation of CD4+25+ regulatory T cells through GITR breaks immunological selftolerance[].Nature Immunology.2002
  • 3Jordan MS,Boesteanu A,Reed AJ,et al.Thymic selection of CD4+25+ regulatory T cells induced by an agaonist self- peptide[].Nature Immunology.2001
  • 4Shevach EM.Control of T cell activation by CD4+ CD25+ suppressor T cells[].Immunological Reviews.2001
  • 5Bystry RS,Aluvihare V,Welch KA,et al.B cells and professional APCs recruit regulatory T cells via CCL4[].Nature Immunology.2001
  • 6Read S,Powrie F.CD4+ regulatory T cells[].Current Opinion in Immunology.2001
  • 7Green EA,Choi Y,Flavell RA.Pancreatic lymph node-derived CD4+25+ T reg cells: highly potent regulators of diabetes that require TRANCE-RANK signals[].Immunity.2002
  • 8Kazuhiko N,Atsushi K,Warren S,et al.Cell contact-dependent immunosuppression by CD4+ 25+ regulatory T cells is mediated by cell surface - bound transforming growth factor -β[].The Journal of Experimental Medicine.2001
  • 9Suto A,Nakajima H,Ikeda K,et al.CD4+ 25+ T-cell development is regulated by at least 2 distinct mechanisms[].Blood.2002
  • 10McHugh RS,Whitters MJ,Piccirillo CA,et al.CD4+25+ immunoregulatory T cells: gene expression analysis reveals a functional role for the glucocorticoid-induced TNF receptor[].Immunity.2002

共引文献55

同被引文献42

引证文献5

二级引证文献5

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