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作 者:朱一蓓[1] 张学光[1] 黄勇[1] 陈成[1] 李文香[1] 戴俊[1] 夏瑜[1] 吴明媛[1]
机构地区:[1]苏州大学医学生物技术研究所
出 处:《中国肿瘤生物治疗杂志》2007年第3期264-268,共5页Chinese Journal of Cancer Biotherapy
基 金:国家自然科学基金重点项目(No30330540)~~
摘 要:目的:研究肿瘤患者外周血单个核细胞来源的树突状细胞(monocyte-deriveddendriticcells,Mo-DC)共刺激分子的表达及其功能。方法:选取11例肺癌、卵巢癌和胃癌患者及10例正常志愿者,分别经粒细胞巨噬细胞集落刺激因子(gran-ulocytemacrophagecolonystimulatingfactor,GM-CSF)和白细胞介素4(IL-4)诱导外周血单个核细胞来源的DC,通过免疫荧光标记和流式细胞术分析、混合淋巴细胞反应(MLR)、FITC-dextran吞噬实验、微孔迁徙实验以及酶联免疫吸附试验(ELISA)等方法比较肿瘤患者和健康志愿者外周血单个核细胞来源DC的表型及功能差异。结果:肿瘤患者来源的Mo-DC在体外诱导早期持续高表达编程死亡-1配体1(programmeddeath-1ligand1,PD-L1),而PD-L2及CCR7、CXCR4的表达则较正常人低(P<0.05);患者来源的Mo-DC分泌高水平的IL-10,体外激发自体T细胞增殖及趋化T细胞尤其是趋化活化T细胞的能力明显低于正常人(P<0.05)。结论:肿瘤患者来源的Mo-DC可能由于自分泌高水平的IL-10和高表达PD-L1而影响其功能的行使。Objective: To investigate the expression of costimulatory molecules of dendritic cells derived from monocytes obtained from the peripheral blood of patients with malignant tumor and their functions. Methods: Peripheral blood samples were obtained from I 1 patients with lung cancer, ovarian cancer, or gastric cancer and 10 normal volunteers; the monocyte-derived dendritic cells were generated in vitro using GM-CSF and IL-4. The phenotypes and functions of DCs derived from healthy volunteers and cancer patients were compared using immunofluorescence, FCT, mixed-lymphocyte reaction, FITC-dextran capture, ELISA, and chemotaxis activity of T lymphocytes. Results: DCs derived from cancer patients expressed higher level of PD-L1 at the early stage of the in vitro culture, but lower levels of PD-L2, CCR7 and CXCR4 compared with those derived from healthy volunteers. DCs derived from cancer patients secreted high level of IL-10 and had a retarded ability to stimulate T cells proliferation and to enrich T cells, especially activated T cells, compared with DCs derived from healthy volunteers. Conclusion: High expression of PD-L1 and autocrine of IL-10 may impair the function of DCs derived from cancer patients.
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