文章摘要
盛红玲柏翠张秋业△ 姜元培.支气管哮喘病儿外周血树突状细胞功能变化[J].,2012,12(8):1482-1485
支气管哮喘病儿外周血树突状细胞功能变化
Function Changes of Dendritic Cells in Peripheral Bloodof Children with Bronchial Asthma
  
DOI:
中文关键词: 支气管哮喘  树突状细胞  共刺激分子  白细胞介素  儿童
英文关键词: Asthma  Dendritic cell  Co-stimulatory molecules  Interleukin  Children
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作者单位
盛红玲柏翠张秋业△ 姜元培 青岛大学医学院附属医院儿科 
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中文摘要:
      目的:观察支气管哮喘病儿外周血单个核细胞(PBMC)来源树突状细胞(DC)功能变化。方法:以18 例健康儿童为对照,选 择16 例支气管哮喘发作期病儿为研究对象,分离PBMC 并经rhGM-CSF 诱生成熟DC。采用流式细胞仪(FACS)检测DC 表面共 刺激分子CD80(B7-1)、CD86(B7-2)和CD83 的表达率;ELISA 法检测培养上清液中IL-10 和IL-12 的变化。结果:①哮喘组DC 表 面CD86 的表达率明显高于健康对照组(t=2.27,P<0.05),CD80、CD83 的表达率与健康对照组比较均无显著性差异(t =1.17,1.34; P>0.05)。②哮喘组DC 分泌IL-10、IL-12 水平均明显低于健康对照组(t'=3.31,3.39;P<0.01)。③哮喘组DC 分泌IL-10 与IL-12 成 正相关(r=0.740,P<0.01),而健康对照组IL-10 与IL-12 无相关性(r=0.232,P>0.05)。结论:支气管哮喘病儿DC 存在功能缺陷, 主要表现在CD86 表达升高、IL-10、IL-12 分泌减少。
英文摘要:
      Objective: To investigate the function changes dendritic cells (DCs) from peripheral blood mononuclear cells (PBMC) in bronchial asthmatic children. Methods: PBMC-derived immature DCs(iDCs) were obtained from peripherial blood samples in 16 asthmatic patients and in 18 healthy children. iDCs were stimulated with rhTNF-α as mature DCs. The expression of the co-stimulatory molecules CD80(B7-1), CD86(B7-2) and CD83 were detected by fluorescent activated cell sorter and the levels of IL-10 and IL-12 in the supernatant were determined by enzyme-linked immunosobent assay. Results: ①The expression of CD86 on DCs was significantly higher than that of healthy control group (t=2.27, P < 0.05). There was no significant difference in the expression of CD80, CD83 between the two groups(t=1.17, 1.34; P > 0.05). ②The level of IL-10 and IL-12 produced from DCs of asthmatic group were significantly lower than that of healthy control group (t'=3.31, 3.39; P < 0.01).③IL-10 had postively relationship with IL-12 in asthma group (r=0.740, P<0.01), while there was no correlation in healthy control group (r=0.232, P > 0.05). Conclusion: DCs dysfunction existed in asthmatic children. It mainly manifested in the increase of the expression of CD86 and the decrease of the secretion of IL-10 and IL-12.
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