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作 者:翟妍[1] 张震宇[1] 王淑珍[1] 乔宝丽[1]
机构地区:[1]首都医科大学附属北京朝阳医院妇产科,100020
出 处:《中国妇幼保健》2008年第13期1850-1852,共3页Maternal and Child Health Care of China
基 金:国家自然科学基金资助项目(编号:39970770)
摘 要:目的:通过负载肿瘤冻融抗原的树突状细胞(DC)预防大鼠卵巢上皮癌发生的体内试验,进行DC疫苗用于卵巢癌防治的可行性研究。方法:取大鼠骨髓单个核细胞(bone marrow mononuclear cells,BMMNC)体外培养获得成熟DC,诱导BMMNC细胞分化的第3天加入大鼠卵巢癌细胞株NuTu-19的冻融抗原,获得负载肿瘤抗原(TAA)的成熟DC;将致敏的DC制成DC疫苗经尾静脉注射大鼠体内,后于大鼠皮下接种NuTu-19细胞,观察大鼠皮下肿瘤的生长情况;注射生理盐水、NuTu-19冻融抗原、未致敏DC作为对照组。结果:大鼠骨髓来源的BMMNC在相关细胞因子的作用下可以培养出成熟的DC。TAA致敏的DC疫苗体内试验中肿瘤发生率较低,成瘤时间较晚,肿瘤生长速度缓慢,与对照组有显著性差别(P<0.01)。结论:大鼠骨髓来源的BMMNC可以培养出成熟的DC。DC可负载并提呈肿瘤抗原,体内试验证明负载癌抗原的DC可以杀伤肿瘤细胞,DC疫苗能够对肿瘤的发生起到主动免疫预防作用,在今后的肿瘤免疫防治方面有着广阔的前景。Objective: To study the feasibility of ovarian tumor cells lysates pulsed dendrite cells in the immunotherapy of tumor prevention in rats. Methods: The bone marrow mononuclear cells (BMMNC) were obtained to sample the mature DC by BMMNC cultured in medium with granulocyte - macrephage colony stimulating factor ( GM - CSF), interleukin -4 (IL -4) and tumor necrosis factor - α. After culturing for 3 days, the rat's ovarian cancer cell line NuTu - 19 freeze - melt antigens were added to pulse DC and acquire the tumor cells lysates pulsed DC. Tumor cells NuTu - 19 were injected to the rats subcutaneous after vaccinating tumor cells lysates pulsed DC via tail vein, and the growth of subcutaneous tumor was observed. For control, saline, NuTu - 19 freeze - melt antigen and not - pulsed DC were injected respectively. Results: The mature DCs were induced by BMMNC co - culturing with relative cytokines, and cell - surface phenotypes were highly expressed. Vaccinating TAA pulsed DC rats had a lower incidence of oncogenesis. There was a significant difference (P 〈 0. 01 ) compare with control group (P 〈0. 01 ) . Conclusion: The mature DC could be obtained from BMMNC. DC could load and submit tumor antigen, which would induce cytotoxic effect for tumor cells invivo. DC vaccine activated T lymphocytes proliferation which induce active immunity against tumor, and it would bring bright prospects in clinical tumor immunotherapy.
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