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作 者:周同[1] 孙桂芝[1] 张玉梅[1] 张雁云[2] 张冬青[2] 陈楠[1]
机构地区:[1]上海第二医科大学瑞金医院肾内科,上海200025 [2]上海第二医科大学上海市免疫学研究所,上海200025
出 处:《现代免疫学》2004年第6期477-481,共5页Current Immunology
基 金:国家自然科学基金资助项目 (3 9970 3 40 ) ;上海市自然科学基金资助项目 (0 2ZB14 0 41;0 3 4119916)
摘 要:观察抗P选择素Lectin EGF功能域单抗 (PsL EGFmAb )对体外培养人树突状细胞 (DC )表型以及促炎细胞因子IL 1 2分泌的影响 ,探讨PsL EGFmAb对DC炎性成熟过程中的调节作用。通过SCF、GM CSF、TGF β1 、Flt 3和TNF α体外培养体系 ,从脐血CD34+ 造血干细胞中诱导扩增获得DC ,并于成熟中用PsL EGFmAb进行干预。采用流式细胞仪分析细胞表型CD1a、CD1 1c、CD83、CD80、CD86和HLA DR ;采用RT PCR检测IL 1 2p35、p4 0mRNA表达 ;以及ELISA法测定IL 1 2p70分泌的含量。结果显示 ,PsL EGFmAb可下调成熟中DC表面CD1 1c、CD83、CD80、CD86和HLA DR的表达 ,同时能抑制DC内IL 1 2p35、p4 0mRNA的转录和IL 1 2p70的分泌。本研究提示 ,PsL EGFmAb对DC黏附共刺激分子表达和促炎细胞因子合成具有抑制作用 。To observe the influence of the monoclonal antibody against Lectin-EGF domain of P-selectin (PsL-EGFmAb) upon the morphologic features of cultured human dendritic cells (DC), as well as the expression of IL-12p35,p40 mRNA and secretion of IL-12p70, CD34+ stem cells from cord blood were isolated and cultured in 20%IMDM medium with SCF,GM-CSF,TGF-β_1,Flt-3,TNF-α. DC were interfered by PsL-EGFmAb.CD1a,CD11c,CD83,CD80,CD86 and HLA-DR was assayed by flow cytometry. IL-12p35,40 mRNA was detected by RT-PCR、IL-12p70 secreted in culture medium was detected by ELISA. It was found that the expression of CD11c,CD83,CD80,CD86 and HLA-DR was lower in PsL-EGFmAb group, and the expression of IL-12p35,40 mRNA and the secretion of IL-12p70 was suppressed after PsL-EGFmAb treatmeut. The PsL-EGFmAb might inhibit the expression of adhesion and co-stimulation molecules, and inhibit proinflammatory cytokine secretion, as well as adjust the antigen presenting function of DC.
关 键 词:树突状细胞 细胞表型 白细胞介素12 抗P选择素Lectin-EGF功能域单抗
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