期刊文献+

肝癌患者CIK细胞的诱导及对肝癌细胞毒作用的研究 被引量:24

Study on the Induction of Cytokine-Induced Killer and the Cytotoxic Effect of These Cells on Hepatocellular Cells
原文传递
导出
摘要 观察肝癌患者PBMC在体外诱导成CIK细胞的能力及其对肝癌细胞的细胞毒作用。对比正常人组和肝癌患者组CIK细胞和LAK细胞之间的扩增差异。用流式细胞仪检测CIK细胞表面标志CD3、CD5 6 ,3 H TdR释放法检测CIK细胞、LAK细胞对肝癌细胞系SMMC 772 1等多种细胞系的细胞毒作用。结果显示 ,肝癌组和正常组的CIK细胞扩增倍数分别达 6 4 3倍和6 7 4倍 ,CD3+CD5 6 +细胞扩增倍数均达 6 0 0倍以上 ,在细胞扩增曲线及细胞表面标志上无差异 ,远大于LAK细胞 ;肝癌组CIK对肝癌细胞SMMC 772 1、Bel 74 0 2、Hep 3b杀伤能力均达 6 5 %~ 81% ,与正常组相同 ,且与对肠癌细胞系HIC 2 5 1杀伤能力无差异 ;对正常胎肝细胞系L 0 2的细胞毒作用 <5 % ;肝癌患者CIK对耐药的和未诱导耐药的K5 6 2细胞细胞毒作用均达到 70 %左右。肝癌患者CIK和正常人CIK一样对肝癌细胞有很强的细胞毒作用 ,对耐药肿瘤同样有效 ,对正常肝细胞无损伤 。 To observe the induction of cytokine induced killer (CIK) in PBMC of patients with liver cell carcinoma and the cytotoxic effect of these cells on the hepatocellular cells (HCC),the differences of amplification of CIK and LAK in patients with liver cell carcinoma and normal adult controls were determined by testing the cell surface markers of CIK,CD3 and CD56 The cytotoxic effects of CIK and LAK to target cells (SMMC 7721) were demonstrated by 3 H TdR release method The results showed that the amplifications of cell growth increased vigorously up to more than 60 times both in HCC group and normal control group,and those of CD3 + and CD56 + cells elevated up to more than 600 times As to the cytotoxicity rate of the expreimental group,it measured as 65%~81%,just as the same as those of the control group
出处 《上海免疫学杂志》 CSCD 北大核心 2003年第3期201-203,209,共4页 Shanghai Journal of Immunology
关键词 CIK 肝癌细胞 肝细胞 细胞毒 3H-TdR释放法 cytokine induced killer liver cell carcinoma cytotoxicity 3H TdR
  • 相关文献

参考文献11

  • 1陶义训 章谷生.临床免疫学检验[M].上海:上海科学技术出版社,1983..
  • 2戴宗晴,李增忱.全方位冷冻治疗中晚期肝癌的研究[J].中华实验外科杂志,1990,7(2):57-58. 被引量:10
  • 3张有顺,戴宗晴.肝癌生物治疗研究进展[J].中国现代普通外科进展,2001,4(4):193-196. 被引量:3
  • 4张有顺,黄玲,袁房均,戴宗晴,王波.肿瘤疫苗对小鼠肝癌作用的研究[J].郧阳医学院学报,2002,21(1):8-11. 被引量:3
  • 5Schmidt-Wolf IG, Negrin RS, Kiem HP, et al. Use of a SCID mouse/human lymphoma model to evaluate cytokine-induced killer cells with potent antitumor cell activ [ 3 ] Schmidt-Woff GD, Negrin RS,Schmidt-Wolf IG. Activated T cells and cytokine-induced CD3+ CD56+ killer cells[J]. Ann Hematol, 1997,74:51.
  • 6Schmidt-Wolf IC, Lefterova P, Johnston V, et al. Sensitivity of multidrug-resistant tumor cell lines to immunologic effector cells[J]. Cell Immunol, 1996,169:85.
  • 7Hoyle C, Bangs CD, Chang P, et al. Expansion of philadelphia chromosome-negative CD3( + )CD56( + ) cytotoxic cells from chronic myeloid leukemia patients:in vitro and in vivo efficacy in severe combined immunodeficiency disease mice[J]. Blood, 1998,92:3318.
  • 8Schmidt-Wolf IG, Finke S,Trojaneck B, et al. Phase Ⅰ clinical study applying autolognus immunological effector cells transfected with the interleukin-2 gene in patients with metastatic renal cancer , colorectal cancer and lymphoma[J]. Br J Cancer, 1999,81 : 1009.
  • 9Schmidt-Wolf IG, Lefterova P, Mehta BA, et al. Phenotypic characterization and identification of effector cells involved in tumor cell recognition of cytokine-induced killer cells [ J ]. Exp Hematol,1993, 21: 1673.
  • 10Lu PH, Negrin RS. A novel population of expanded human CD3+ CD56+ cells derived from T cells with potent in vivo antitumor activity in mice with severe combined immunodeficiency [J]. J Immunol,1994, 153: 1687.

二级参考文献3

共引文献19

同被引文献149

引证文献24

二级引证文献160

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