李金凤, 张震宇, 王淑珍, 刘晋玮. 卵巢癌细胞和脐血树突状细胞融合瘤苗抗肿瘤免疫效应的初步研究[J]. 中国肿瘤临床, 2007, 34(14): 789-793.
引用本文: 李金凤, 张震宇, 王淑珍, 刘晋玮. 卵巢癌细胞和脐血树突状细胞融合瘤苗抗肿瘤免疫效应的初步研究[J]. 中国肿瘤临床, 2007, 34(14): 789-793.
Li Jinfeng, Zhang Zhenyu, Wang Shuzhen, . The Anti-tumor Immune Response to Ovarian Cancer Cells Fused to Dendritic Cells Derived from Cord Blood In Vitro[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 34(14): 789-793.
Citation: Li Jinfeng, Zhang Zhenyu, Wang Shuzhen, . The Anti-tumor Immune Response to Ovarian Cancer Cells Fused to Dendritic Cells Derived from Cord Blood In Vitro[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 34(14): 789-793.

卵巢癌细胞和脐血树突状细胞融合瘤苗抗肿瘤免疫效应的初步研究

The Anti-tumor Immune Response to Ovarian Cancer Cells Fused to Dendritic Cells Derived from Cord Blood In Vitro

  • 摘要: 目的 :将脐血来源的树突状细胞(DC)与人卵巢癌细胞株SKOV3细胞相融合,获得SKOV3/DC融合细胞,分析其生物学特性及体外诱导抗卵巢癌肿瘤免疫的能力。 方法 :1)将用pKH26红色荧光染料标记脐血来源的DC后,聚乙二醇法(PEG)融合DC与人卵巢癌细胞株SKOV3细胞,流式细胞仪分选融合细胞。2)应用细胞培养技术、流式细胞术及光学显微镜检测SKOV3/DC的生长特性和形态学特征;四甲基偶氮唑蓝(MTT)法观察融合细胞体外刺激混合淋巴细胞反应的能力及诱导特异性肿瘤免疫的能力。 结果 :1)DC和SKOV3按10:1比例融合,融合率约为8.5%。融合细胞可在体外缓慢增殖,CA125抗原及CD1a、CD80、CD86、HLA-DR、MHC-I分子表达阳性。2) SKOV3/DC在体外能有效的激发混合淋巴细胞增殖反应,可明显激活细胞毒性T淋巴细胞(CTL),对卵巢癌细胞株SKOV3有特异性杀伤效应。 结论 :利用PEG法制备的SKOV3/DC融合细胞兼具两种亲本细胞的部分特性,在体外能够诱导特异性抗肿瘤免疫。本研究将SKOV3/DC作为肿瘤疫苗,为其在卵巢癌主动免疫治疗研究中的进一步应用打下了基础。

     

    Abstract: Objective : To prepare hybrid SK0V3/DC cells by fusing dendritic cells (DC) derived from cord blood and SK0V3 ovarian cancer cells and to analyze anti-tumor immune response to ovari-an cancer cells in vitro. Methods : 1) Using polyethylene glycol (PEG) SK0V3 cells were fused to DC that was then stained with red fluorescent PKH26. The SK0V3/DC fused cells were selected by flow cytometry. 2) Flow cytometry and light microscopy were used to study the morphology of SK0V3/DC in vitro. MTT assay was used to detect the fused cells" ability to activate a mixed lymphocyte reaction. The killing action of the specific anti-tumor immune response was also assessed. Results : 1) The DC were fused with SK0V3 cells at a ratio of 10:1 and the fusion rate was about 8.5%. SK0V3/DC could prolif-erate slowly in vitro and expressed CA125, CD I a, CD80, CD86, HLA-DR, and MHC-I molecules. 2) SKOV3/DC could stimulate a mixed lymphocyte reaction (MLR) efficiently in vitro; SKOV3/DC could activate cytotoxic T lymphocytes that could kill the SKOV3 cells specifically. Conclusion : SKOV3/DC obtained by PEG treatment have some characteristics of both parental cells and were capa-ble of inducing a specific anti-tumor immune response to ovarian cancer cells in vitro. These data sim-ulating an SKOV3/DC vaccine provide evidence for effective immunotherapy against ovarian cancer.

     

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