Suppr超能文献

[植物血凝素对细胞因子诱导的杀伤细胞增殖及细胞毒性的影响]

[Effect of phytohemagglutinin on proliferation and cytotoxicity of cytokine-induced killer cells].

作者信息

Qin Fu-Li, Zhang Shao-Lin, Sun Hui, Xi Yu-Ren

机构信息

Department of Hematology, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2005 Feb;13(1):118-20.

Abstract

The purpose was to investigate the effect of phytohemagglutinin (PHA) on proliferation and cytotoxicity of cytokine-induced killer (CIK). Peripheral blood mononuclear cells (PBMNCs) from healthy donors were divided into two groups. Cells were resuspended and maintained in complete medium containing of 10% autologous plasma. CIK cells were cultured by traditional method in group one. The other group cells were added PHA to stimulate PBMNCs for 24 hours, then cultured like incubating CIK cells. Their cytotoxicity to different target cells was evaluated by (51)Cr release assay. The results showed that the proliferation multiples of CIK and PHA-CIK cells were both high, however, the latter was much higher than CIK with significance (P < 0.05). Cells in each group cells showed high cytotoxicity. At the same high effector/target ratio PHA-CIK cells cytotoxicity was stronger than CIK cells when targets were K562 cells or acute leukemia cells (P < 0.05). In conclusion, PHA-CIK cells exhibit stronger proliferation and cytotoxicity than CIK cells, and the result provides an experimental basis for biotherapy.

摘要

目的是研究植物血凝素(PHA)对细胞因子诱导的杀伤细胞(CIK)增殖和细胞毒性的影响。将健康供者的外周血单个核细胞(PBMNCs)分为两组。细胞重悬于含10%自体血浆的完全培养基中并维持培养。第一组采用传统方法培养CIK细胞。另一组细胞加入PHA刺激PBMNCs 24小时,然后像培养CIK细胞一样进行培养。通过(51)Cr释放试验评估它们对不同靶细胞的细胞毒性。结果显示,CIK细胞和PHA - CIK细胞的增殖倍数均较高,但后者显著高于CIK细胞(P < 0.05)。每组细胞均表现出高细胞毒性。在相同的高效应细胞/靶细胞比例下,当靶细胞为K562细胞或急性白血病细胞时,PHA - CIK细胞的细胞毒性强于CIK细胞(P < 0.05)。总之,PHA - CIK细胞比CIK细胞表现出更强的增殖能力和细胞毒性,该结果为生物治疗提供了实验依据。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验