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细胞趋化因子受体-5和CD57在自身免疫性甲状腺疾病中的表达及意义
引用本文:张健,李翠,秦秋,朱远凤,杨香菊,王璇,张进安.细胞趋化因子受体-5和CD57在自身免疫性甲状腺疾病中的表达及意义[J].综合临床医学,2012(4):337-340.
作者姓名:张健  李翠  秦秋  朱远凤  杨香菊  王璇  张进安
作者单位:[1]复旦大学附属金山医院检验科,上海201508 [2]西安交通大学医学院第一附属医院内分泌科 ,上海201508 [3]复旦大学附属金山医院内分泌科,上海201508
基金项目:国家自然科学基金资助项目(81070627)
摘    要:目的通过观察滤泡辅助T细胞(Tfh细胞)相关因子细胞趋化因子受体_5(CXCR5)及CD57在桥本甲状腺炎及Graves病患者甲状腺的表达,探讨个m细胞在自身免疫性甲状腺疾病发生中的作用。方法利用免疫组织化学sP法检测CXCR5、CD57在15例桥本甲状腺炎及18例Graves病患者甲状腺的表达,以10例正常甲状腺组织为对照组。结果CXCR5、CD57在桥本甲状腺炎及Graves病主要表达于浸润淋巴细胞的胞膜和胞质,CXCR5阳性率分别为93.3%(14/15)和88.9%(16/18),CD57表达的阳性率分别为93.3%(14/15)和83.3%(15/18),均显著高于正常对照(P均〈0.05),两种分子在桥本甲状腺炎和Graves病中的表达差异无统计学意义(P〉0.05)。结论CXCR5及CD57主要表达在甲状腺组织浸润的淋巴细胞的胞质和胞膜,且在两种自身免疫性甲状腺疾病中的表达呈现一致性,提示Tfh细胞参与了自身免疫性甲状腺疾病的发生。

关 键 词:桥本甲状腺炎  Graves病  细胞趋化因子受体-5  CD57

The expression of CXCR5 and CD57 in autoimmune thyroid diseases
Authors:ZHANG Jian  LI Cui  QIN Qiu  ZHU Yuan-feng  YANG Xiang-ju  WANG Xuan  ZHANG Jin-an
Institution:. Department of Clinical Laboratory, Jinshan Hospital Fudan University, Shanghai 201508, China Corresponding author : ZHANG Jin-an, Email :zhangiinan@ hotmaiL corn
Abstract:Objective To investigate the potential role of T follicular helper cells (Tfh) in the pathogenesis of autoimmune thyroid diseases by comparing the expression of C-X-C chemokine teceptor type 5 (CXCRS) and CD57 in Hashimoto's thyroiditis (HT) and Graves' disease (GD) thyroid tissues. Methods The expression of CXCR5 and CD57 proteins was determined by immunohistochemical analysis in 15 HT thyroid samples, 18 GD samples and 10 normal thyroid samples. Results Immunohistochemical staining showed that CXCR5 and CD57 were mainly positive in cytomembrane and cytoplasm of the infiltrated lymphocytes both in HT and GD tissues, with much higher levels than that of normal thyroid tissues (P 〈 0.05 ). Both CXCR5 and CD57 were not significantly different between the HT and GD tissues. Conclusion CXCR5 and CD57 expressions were increased with a similar expression pattern in both of the two main autoimmune thyroid diseases( AITD), indicating that Tfh may participate in the development and progression of AITD.
Keywords:Hashimoto's thyroiditis  Graves' disease  C-X-C chemokine receptor type 5  CD57
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