耐药乳腺癌免疫治疗的实验研究  被引量:2

Pilot Study of Immunization Therapy on Drug-Resistance in Breast Cancer Bearing Mouse Model

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作  者:司玉玲[1] 庞华[1] 綦振家[1] 乔丽葵[2] 王英娟[1] 李世俊[1] 

机构地区:[1]天津市第四中心医院肿瘤血液科,300140 [2]天津市第四中心医院肿瘤病理科

出  处:《天津医药》2012年第4期359-362,I0004,共5页Tianjin Medical Journal

基  金:天津市自然科学基金资助项目(项目编号:09JCYBJC10600)

摘  要:目的:探讨耐药乳腺癌抗原负载的树突细胞(DC)与细胞因子诱导的杀伤细胞(CIK)联合培养后对同种乳腺癌荷瘤小鼠的可能治疗机制。方法:分离健康人外周血获得单个核细胞,分别诱导为DC和CIK细胞,将人类乳腺癌耐药细胞株MCF-7/ADR细胞的冻融物抗原冲击DC(AP-DC),分别将DC与CIK细胞共培养(AP-DC+CIK组、DC+CIK组),将细胞经尾静脉注入裸鼠体内,观察不同组荷瘤标本中MDR1的表达、肿瘤细胞凋亡及凋亡相关蛋白Bax和Bcl-2的表达。结果:AP-DC+CIK组、DC+CIK组、CIK组及生理盐水组MDR1/β-actin比值分别为0.14、0.57、0.81及0.98。生理盐水组、CIK组、DC+CIK组和AP-DC+CIK组平均凋亡指数差异有统计学意义(P<0.001)。各组Bcl-2及Bax蛋白表达的OD值差异有统计学意义(P<0.01),Bcl-2/Bax值AP-DC+CIK组<DC+CIK组<CIK组<生理盐水组。结论:经耐药乳腺癌抗原负载的DC与CIK共同作用后,诱导同种乳腺癌细胞凋亡强于单纯DC与CIK共同作用后及单独CIK的治疗效果。Objective: To explore the possible mechanisms of immunization therapy, cytokine-induced killer (CIK) cells co-cultured with dendritic cells (DC), on mutidrug-resistance breast cancer bearing mouse model. Methods: DC and CIK were cultured respectively from peripheral blood mononuclear cells (PBMC) derived from healthy individuals. MCF-7/ ADR, a kind of breast cancer cell line with multidrug resistance, was prepared to obtain the antigen lyses. CIK was co-cul- tured with DC pulsed or unpulsed by the above antigen lyses (AP-DC+CIK and DC+CIK). The effector cells were injected into the tumor-bearing mice through tail intravenous. The expression of MDR1, tumor cell apoptosis and the expression of Bcl-2 and Bax were measured in 4 types of cells. Results:The ratio of MDR1 to β-actin was different in the above 4 types of cells, AP-DC+CIK group was 0.14, DC+CIK group was 0.57, CIK groupwas 0.81, and normal saline (NS) group was 0.98. The average apoptosis index was also significantly different in these 4 groups (P 〈 0.001). The values of optical density (OD) of protein Bcl-2 and Bax were different in 4 types of cells (P 〈 0.05). The value of Bcl-2/Bax was the lowest in AP-DC+CIK group, and then followed by DC+CIK group and CIK group. The value of Bcl-2/Bax was the highest in NS group. Conclu- sion: After CIK cells were co-cultured with DC loaded with multidrug resistance breast cancer antigen, the apoptosis of these breast cancer cells was higher than those of CIK cells co-cultured with DC and those of CIK.

关 键 词:树突细胞 杀伤细胞 淋巴因子激活 BCL-2相关X蛋白质 乳腺肿瘤 抗药性 肿瘤 疾病模型 动物 

分 类 号:R28[医药卫生—中药学]

 

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