机构地区:[1]河北医科大学第四医院暨河北省肿瘤研究所,河北石家庄050011 [2]第四军医大学西京医院肿瘤科,陕西西安710030
出 处:《中国肿瘤生物治疗杂志》2012年第4期374-380,共7页Chinese Journal of Cancer Biotherapy
基 金:河北省科技计划资助项目(No.09276101D-29);河北省高校强势特色学科资助项目(No.200552)~~
摘 要:目的:探讨细胞因子诱导的杀伤细胞(cytokine-induced killer cell,CIK)对荧光素酶标记的人宫颈癌HeLa-luc细胞的体内外抗肿瘤作用,了解CIK回输荷瘤小鼠后在不同器官的分布特点。方法:由健康志愿者外周血单个核细胞体外诱导培养CIK,流式细胞术检测CIK表面分子的表达,RT-PCR法检测IFN-γmRNA的表达,MTT法和瑞氏-姬姆萨染色测定CIK对HeLa-luc细胞的杀伤作用。建立荷HeLa-luc瘤BALB/c裸鼠模型,体内成像系统观察荷瘤小鼠肿瘤大小变化及CIK治疗效果,共聚焦显微镜观察不同器官中CIK的分布情况。结果:CIK在体外诱导培养14~21 d,其生长达到高峰,此时CD3+CD56+T细胞的比例增加50倍以上,IFN-γmRNA表达水平也达到高峰。在效靶比为20∶1、40∶1时,CIK对HeLa-luc细胞的杀伤率分别为(51.16±2.64)%、(72.14±4.21)%,明显高于对照组的(16.33±3.09)%、(21.26±2.71)%(P<0.05)。CIK治疗5周和8周后,对荷瘤小鼠的抑瘤率分别为47.18%、64.38%。CIK治疗组荷瘤小鼠外周血中IFN-γ水平为(61.92±6.49)pg/ml,明显高于对照组的(34.30±1.78)pg/ml(P<0.05)。CFSE标记的CIK经腹腔和瘤旁注射入荷瘤小鼠3 h,在肺、肝、脾、外周血、肿瘤中均可观察到绿色荧光;腹腔途径注射24 h时,肿瘤组织中CIK浓度达到高峰(20.56±1.72)%;瘤旁途径注射3 h时,肿瘤组织中CIK达到高峰(25.75±3.45)%。结论:CIK在体内外对宫颈癌HeLa-luc细胞均有较强的杀伤作用,CIK经不同途径注射荷瘤小鼠后可以广泛分布于全身器官,其到达各脏器的浓度与输注途径及时间密切相关。Objective: To study the anti-tumor activity of cytokine-induced killer cells (CIK cells) against HeLa-luc cells (cervical cancer HeLa ceils labeling luciferase) in vivo and in vitro, and to analyze the distribution characteristics of CIK cells in different organs in a mouse xenograft model of cervical cancer nude. Methods: CIK cells were induced from peripheral blood mononuclear cells of health volunteers and cultured in vitro. The phenotype of CIK ceils were determined by flow cytometry. The expression of IFN-γ mRNA in CIK ceils was detected by RT-PCR assay. The killing activity of CIK cells on HeLa-luc cells was determined by MTF assay and Wright-Giemsa' s staining. HeLa-luc cell-bearing BALB/c nude mouse model was established. Tumor size changes and treatment effect were detected using in vivo Xenogen IVIS Im- aging System. The distribution characteristics of CIK cells in different organs were detected by confocal microscopy. Results : CIK cells grew up to the peak after being cultured for 14-21 d. The percentage of CD3 ^± CD56 ^± T cells was increased more 50 times than that of the beginning. The expression level of IFN-γ mRNA in CIK cells was also increased to the peak. When the ratios of effect to target were 20: 1, and 40: 1, the cytotoxicity of CIK cells on HeLa-luc cells was (51.16 ± 2.64) % and (72.14% ± 4.21 ) %, respectively, and was significantly higher than that of the control group ( [ 16. 33 ± 3.09 ] %, [ 21.26 ± 2.71]%, respectively, P 〈 0.05 ). The inhibitory rate of CIK cells on the tumor was 47.18% and 64.38% at the fifth week and the eighth week, respectively. The level of IFN-3, mRNA in the CIK experi- ment group (61.92 ± 6.49) pg/ml was significantly higher than that in the control group (34.30 ± 1.78 ) pg/ml (P 〈 0. 05 ). Green fluorescence can be observed in the lung, liver, spleen, peripheral blood and tumor tissues under the con- focal microscope 3 h after CFSE-labeled CIK cells injection via peritoneal cavity and tumor adjacent.
关 键 词:细胞因子诱导的杀伤细胞 宫颈癌 HeLa—luc细胞 IFN-γ 抗肿瘤作用 体内分布
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