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CD_3AK 细胞、环磷酰胺和硒酸酯多糖联合治疗小鼠白血病的研究 被引量:10

Biotherapeutic efficacy of adoptive transfer of CD 3AK cells in combination with cyclophosphamide and kappa selenocarrageenan in P 388 leukemic mice
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摘要 目的:为探讨DBA/2小鼠脾淋巴细胞诱生的抗CD3单克隆抗体(单抗)激活的杀伤细胞(CD3AK细胞)过继输入及联合化疗和生物反应调节剂对小鼠白血病的治疗作用。方法:将P388细胞移植到DBA/2小鼠腹腔建立白血病模型,用抗CD3单抗和小剂量重组白细胞介素2(rIL-2)从小鼠脾细胞中诱生CD3AK细胞。检测淋巴细胞转化率、NK细胞活性和脾淋巴细胞IL-2诱生水平以及荷瘤鼠生存期。结果:小鼠接种P388细胞后细胞免疫功能(淋巴细胞转化率、NK活性和IL-2水平)明显减低。转输CD3AK细胞和小剂量rIL-2,小鼠生存期延长(45.19%),细胞免疫功能显著增强;单纯化疗可以延长小鼠生存期(29.90%),但却使免疫功能低下的荷瘤鼠的T细胞和NK细胞功能进一步降低,与CD3AK细胞转输联合可阻止化疗所致的免疫功能的降低,生存期进一步延长(59.45%),并有25%的小鼠长期存活;硒酸酯多糖与CD3AK细胞或CD3AK细胞+化疗联合应用治疗效果最佳,12.5%~75.0%小鼠长期存活,且体内未发现有白血病细胞存在。结论:硒酸酯多糖是一种实用而有效的生物反应调节剂,肿瘤杀伤效应细胞+化疗+生物反应调节剂方案是一种白? Objective:To study the antileukemia efficacy of a combination of adoptive transfer of CD 3AK cells, cyclophosphamide(CTX) , and kappa selenocarrageenan(KSC)in P 388 leukemic mice.Methods:CD 3AK cells in normal DBA/2 murine splenocytes were induced with anti CD 3 antibody and low dose recombinant interleukin 2 (rIL 2).The P 388 murine leukemia model was induced by i.p.injection of P 388 cells into normal DBA/2 mice.The tumor bearing mice were administrated with adoptively transferred CD 3AK Cells and/or CTX and/or KSC.Results:After tumor inoculation ,the cellular immune function of P 388 bearing mice was supressed markedly.Adoptive transfer of CD 3AK cells with low dose rIL 2 into the P 388 mice significantly enhanced the splenocyte proliferation (SP) induced by Con A ,the NK cell activity and the splenocytic IL 2 production and prolonged their survival(45.19%);CTX(200 mg/kg) alone prolonged the survival of P 388 bearing mice(29.90%),but further decreased the immunodeficiency ; combination of CTX and CD 3AK passive transfer could prevent the reduction of SP,NK activity and IL 2 production in the leukemic mice and prolonged the survival(59.45%),combination of KSC and adoptively transfected CD 3AK cells and/or CTX had a much better therapeutic efficacy for P 388 murine leukemia,12.50%~75.00% of the leukemic mice were cured.Conclusion:KSC is a hopeful biological response modifier in cancer biotherapy,and tumor killing effector cells and chemotherapy plus BRM might be a promising candidate for human leukemia biotherapy.
出处 《中华血液学杂志》 CAS CSCD 北大核心 1997年第5期243-246,共4页 Chinese Journal of Hematology
关键词 CD3AK细胞 环磷酰胺 硒酸酯多糖 白血病 CD 3AK cells Cyclophosphamide Kappa selenocarrageenan Leukemia,experimental Biotherapy
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参考文献5

  • 1魏虎来,兰州大学学报,1996年,32卷,122页
  • 2魏虎来,免疫学杂志,1995年,11卷,104页
  • 3牛桂莲,中华微生物学和免疫学杂志,1995年,15卷,86页
  • 4毕爱华,医学免疫学,1995年
  • 5王文涛,中国药理学与毒理学杂志,1994年,8卷,199页

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