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机构地区:[1]山东省医学科学院基础所免疫室,济南市250062
出 处:《中国肿瘤临床》1997年第11期845-848,共4页Chinese Journal of Clinical Oncology
摘 要:应用抗CD3单克隆抗体和基因重组人IL-2共同诱导人外周血单个核细胞,制备抗CD3单克隆抗体活化的杀伤细胞(CD3AK)。利用LDH释放法,观察顺氨氯铂(CDDP)和阿霉素(ADM)预处理人肝癌细胞系H-7402,对CD3AK杀伤该靶细胞的调节作用。ABC-ELISA法检测CDDP和ADM对H-7402细胞表达细胞间粘附分子-1(ICAM-1)、HLA-ABC、HLA-DR抗原的影响。结果表明:经CDDP(2.0μg/ml)、ADM(O.1μg/ml)预处理12h的H-7402细胞对CD3AK的杀伤敏感性显著提高(P<0.05);CDDP能够明显促进H-7402细胞表达ICAM-1、HLA-ABC分子(P<0.05);ADM预处理的肿瘤细胞表面三种分子的表达均未发生明显的变化。CDDP促进人肝癌细胞对CD3AK的杀伤敏感性可能与其上调了肿瘤细胞表面的ICAM-1分子有关。Human CD3AK cells were prepared from peripheral blood mononuclear cells by culturing them in recombinant IL-2 and anti CD3McAb. The vulnerabi lity H-7402 pretreated with CDDP or ADM to lysis by CD3AK, and the expression of ICAM-1, HLA-ABC, HLA-DR antigen induced by CDDP or ADM were examined. The result showed that pretreatment of H-7402 cells with CDDP (2ug/ml) or ADM (0. 1ug/ml) for 12 hrs resulted in increased vulnerability of these cells to CD,AK-mediated killing (P<0. 05). The expression of ICAM-1, HLA-ABC but not HLA-DR on H-7402 cells were increased after treatment of the tumor cells with CDDP (P<0. 05). However, ADM showed no regulation effect on the expression of the surface antigens on H-7402 cells. The results suggest that enhancement of CD3AK-mediated cytotoxicity by CDDP may probably be correlated with the modulation of ICAM-1 molecule on H-7402 cells.
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