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CIK细胞治疗晚期肝癌的临床观察 被引量:6

Clinical Study on the Treatment of Patients with Advanced Liver Cancer by CIK Cells
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摘要 目的观察CIK细胞治疗晚期肝癌的临床疗效。方法体外培养CIK细胞,14 d后分次回输给患者,观察患者治疗前后瘤体大小、肿瘤标志物、免疫指标、临床症状、生活质量、卡氏评分等的变化,并记录生存期。结果晚期肝癌治疗前后肿瘤标志物CA199和AFP比较差异有统计学意义(P<0.05),CD4、CD19、CD3/CD16+CD56+比较差异均有统计学意义(P<0.05);治疗后患者临床症状比治疗前有明显改善,差异有统计学意义(P<0.05);卡氏评分提高率为73.91%。结论CIK细胞疗法为无手术放疗及化疗适应证的晚期肝癌患者提供了一种延长生存期,改善生活质量的新途径。 Objective To estimate the clinical eftects on patients with advanced liver cancer by cytokine-induced killer cells (CIK). Meth- ods CIK cells were cultured in vitro,then were transfused back to 46 patients with advanced liver cancer after two weeks. The changes of tumor weight, immunity indexes, tumor markers, life quality, and the Karnofsky' s grade were observed, and the survival time was recorded. Results The CA199 and AFP from patients with advanced liver cancer after treatment are significantly lower than that before treatment (P 〈 0.05), the CD4, CD19, CD3/CD16^+ CD56^+ from patients with liver cancer after treatment were significantly higher than that before treatment (P 〈 0.05 ). The clinical symptoms of patients after treatment have a significant improvement as compared with before treatment. Karnofsky' s grade increased rate was 73.91%. Conclusion CIK cells therapy can improve survival quantity and prolong survival period, which probably provide a new strategy for patients with advanced liver cancer.
出处 《肿瘤基础与临床》 2009年第6期505-507,共3页 journal of basic and clinical oncology
关键词 晚期肝癌 CIK细胞 过继免疫疗法 advanced liver cancer CIK cells adoptive immunotherapy
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  • 1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
  • 2陈复兴 刘军权 等.人PBMC经数种活化剂活化后的表型变化[J].中国肿瘤生物治疗杂志,1999,6:186-187.
  • 3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..
  • 4陈复兴 刘军权 等.抗人CD3单克隆抗体体外诱导T细胞和肿瘤浸润性淋巴细胞增殖的研究[J].南京部队医药,1994,5:15-17.
  • 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.

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