索拉非尼联合树突状细胞与细胞因子诱导的杀伤细胞对肝癌生长与侵袭转移的作用

Effects of sorafenib combined with dendritic cells and cytokine induced killer cells on the growth and invasion and metastasis of hepatocellular carcinoma

  • 摘要: 目的:探讨索拉非尼联合树突状细胞(DC)与细胞因子诱导的杀伤细胞(CIK)对肝癌生长与侵袭转移的作用。
    方法:采集健康自愿者外周血50 mL,体外培养健康成人细胞因子诱导的DC和CIK。160只雄性ICR小鼠建立H22肝癌细胞小鼠原位肝癌模型,采用随机数字表法分为4组:(1)生理盐水组:仅经胃灌注与索拉非尼组同等的生理盐水;(2)索拉非尼组:经胃灌注索拉非尼100 μg/g,1次/d;(3)DC-CIK细胞组:经腹腔注射DC-CIK共培养细胞,1×10 7/只,1次/3 d;(4)索拉非尼联合DC-CIK 细胞组:经胃灌注索拉非尼,同时腹腔注射DC-CIK共培养细胞,剂量同前。每组40只,治疗3周,各组取20只处死,获取外周血和肝脏肿瘤组织。采用ELISA法检测AFP水平,HE染色检测肿瘤坏死程度,免疫组织化学染色分别检测肿瘤组织Ki-67和CD34表达。各组余下20只小鼠,观察生存时间。多组比较采用单因素方差分析,组间比较采用LSD检验。
    结果:DC和CIK诱导、培养成功。生理盐水组、索拉非尼组、DCCIK组和索拉非尼联合DC-CIK组AFP分别为(0.675±0.177)ng/L、(0.379±0.052)ng/L、(0.415±0.028)ng/L和(0.288±0.012)ng/L,4组比较,差异有统计学意义( F=0.415,P <0.05)。生理盐水组肝内和腹腔转移数目分别为(21.2±1.3)个和(29.7±7.6)个,索拉非尼组分别为(16.4±1.6)个和(17.4±1.8)个,DC-CIK组分别为(20.2±1.7)个和(26.4±1.7)个,索拉非尼联合DC-CIK组分别为(15.2±1.3)个和(15.2±1.3)个,4组比较,差异有统计学意义( F=2.137,3.271,P <0.05)。生理盐水组、索拉非尼组、DC-CIK组和索拉非尼联合DC-CIK组抑瘤率分别为0、21% ±5%,4组比较,差异有统计学意义( F=3.715,P <0.05)。生理盐水组、索拉非尼组、DC-CIK组和索拉非尼联合DC-CIK组生存时间分别为(18.2±2.5)d、(21.6±2.1)d、(24.3±2.8)d和(25.4±1.4)d,4组比较,差异有统计学意义( F=6.247,P <0.05)。
    结论:索拉非尼联合DC与CIK免疫治疗能够显著延长肝癌荷瘤小鼠生存时间,抑制肝肿瘤生长和转移。

     

    Abstract: Objective:To investigate the effects of sorafenib combined with dendritic cells and cytokine induced killer (DC CIK) cells on the growth, invasion and metastasis of hepatocellular carcinoma.
    Methods: CIK cells and dendritic cells from healthy adults were cultured in vitro . Mice models with H22 hepatic cancer were established, and randomly divided into the normal saline group, sorafenib group, DC CIK group and the sorafenib+DC CIK group according to the random number table. There were 40 rats in each group. All the mice received intragastric gavage with sorafenib of 100 μg/g once a day. DC CIK cells were intraperitoneally injected into the mice every 3 days with 1×10 7 cells each time. Twenty mice bearing tumors in each group were sacrificed after treatment for 3 weeks, and the peripheral venous blood and hepatic tumor tissues were harvested. The levels of alpha fetoprotein (AFP) were detected by ELISA, and the necrotic degree of tumor tissues was evaluated by 〖HJ*4〗hematoxylin and eosin staining. The protein expressions of Ki -67 and CD34 in the tumor tissues were determined by immunohistochemical method. The survival time of the other 20 mice bearing the tumor in each group were detected. All data were analyzed using the analysis of variance or LSD test.
    Results:CIK cells and dendritic cells were successfully cultured. The levels of AFP in the peripheral venous blood of the normal saline group, sorafenib group, DC CIK group and sorafenib+DC CIK group were (0.675±0.177)ng/L, (0.379±0.052)ng/L, (0.415 ±0.028)ng/L, (0.288±0.012)ng/L, with significant difference between the 4 groups ( F=0.415, P <0.05) . The numbers of intrahepatic and peritoneal metastasis of  the normal saline group, sorafenib group, DC CIK group and sorafenib+DC CIK group were 21.2±1.3 and 29.7±7.6, 16.4±1.6 and 17.4±1.8, 20.2±1.7 and 26.4±1.7, 15.2±1.3 and 15.2±1.3, with significant difference between the 4 groups ( F= 2.137, 3.271, P <0.05).  The tumor inhibition rate of the normal saline group, sorafenib group, DC CIK group and sorafenib+DC CIK group were 0, 21% ±5%,with significant difference between the 4 groups ( F=3.715, P< 0.05). The survival time of mice in  the normal saline group, sorafenib group, DC CIK group and sorafenib+DC CIK group were (18.2±2.5)days, (21.6±2.1)days, (24.3±2.8)days and (25.4±1.4)days, with significant difference between the 4 groups ( F=6.247, P <0.05).
    Conclusions: Sorafenib combined with immunotherapy can significantly increase the therapeutic effects of molecular targeted drug on hepatocellular carcinoma.

     

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