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作 者:满琦[1] 张安[1] 张源[2] 樊明德[1] 马道新[3] 王成伟[1]
机构地区:[1]山东大学第二医院神经外科,山东济南250033 [2]山东大学齐鲁医院急诊科,山东济南250012 [3]山东大学齐鲁医院血液科,山东济南250012
出 处:《山东大学学报(医学版)》2016年第10期55-59,70,共6页Journal of Shandong University:Health Sciences
基 金:山东省自然科学基金(ZR2013HM083)
摘 要:目的探究脑胶质瘤患者外周血中Th17、Th22细胞的表达及意义。方法取34例脑胶质瘤患者及24例健康对照者为研究对象,用流式细胞术检测外周血中Th17、Th22细胞的表达比例。用实时荧光定量逆转录聚合酶链反应(RT-PCR)技术检测外周血单个核细胞中视黄酸相关孤儿核受体(RORC)mRNA及芳香烃受体(AHR)mRNA的表达。用酶联免疫吸附分析(ELISA)检测血浆中Th22细胞相关因子白细胞介素-22(IL-22)的水平。结果与健康对照组相比,脑胶质瘤患者外周血Th17细胞比例(占淋巴细胞)升高不明显(P>0.05),且高级别组(WHOⅢ-Ⅳ级)与低级别组(WHOⅠ-Ⅱ级)之间差异不明显(P>0.05);Th22细胞比例(占淋巴细胞)明显升高(P<0.05),且不同级别之间差异明显(P<0.05)。脑胶质瘤患者Th17与Th22细胞呈正相关(r=0.40,P=0.03),健康对照组中二者无相关(P>0.05)。与健康对照组比较,患者外周血中RORC mRNA及AHR mRNA的升高不明显(P>0.05,P>0.05),且不同级别间差异不明显(P>0.05,P>0.05)。患者血浆IL-22水平比健康对照组明显升高(P<0.05),但不同级别之间差异不明显(P>0.05)。结论脑胶质瘤患者外周血中存在Th22细胞及IL-22异常升高,Th17细胞与Th22细胞可能共同参与胶质瘤的发生发展过程。Objective To investigate the expression and significance of Thl7 and Th22 cells in the peripheral blood of patients with glioma. Methods A total of 34 patients with glioma and 24 normal controls were enrolled. The percenta- ges of Thl7 and Th22 cells in peripheral blood were measured by flow cytometry. Retinoid-related orphan nuclear receptor (RORC) and arylhydrocarbon receptor (AHR) mRNA in peripheral blood mononuclear cells were detected by reverse-transcriptional polymerase chain reaction (RT-PCR). The plasma level of interleukin-22 (IL-22) was detected by ELISA. Results There was no difference between patients and healthy controls in circulating Thl7 cells (P 〉 0.05 ), and no difference was found between the high-grade group ( WHO Ⅲ -Ⅳ ) and low-grade group ( WHO Ⅰ - Ⅱ ) ( P 〉 0.05 ). The percentage of circulating Th22 cells in glioma was significantly increased compared with that in controls ( P 〈 0.05 ), and the difference between different grade groups was obvious ( P 〈 0.05 ). A positive correlation between Th22 and Thl7 cells was observed in glioma ( r = 0. 40, P = 0.03 ), no correlation was found in controls ( P 〉 0.05 ). The difference of RORC and AHR between patients and controls was not significant ( P 〉 0. 05, P 〉 0.05 ),and no difference was found between different grade groups ( P 〉 0. 05, P 〉 0.05 ). The serum IL-22 level in patients was significantly increased compared with that in controls ( P 〈 0.05 ). However, there was no difference of serum IL-22 levels between different grade groups (P 〉 0.05). Conclusion There exist abnormal increases of Th22 cells and IL-22 levels in the peripheral blood of glioma, and Thl7 and Th22 cells may jointly participate in the pathogenesis and progression of glioma.
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