IL-17A及Th17在炎症性肠病中的作用  被引量:9

Role of IL-17A and Th17 in inflammatory bowl disease

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作  者:杨淑萍[1] 智绪亭[2] 卢雪峰[1] 冯立娟[1] 王琴伊[1] 

机构地区:[1]山东大学齐鲁医院消化内科,山东济南250012 [2]山东大学齐鲁医院普外科,山东济南250012

出  处:《中国现代普通外科进展》2009年第3期222-225,共4页Chinese Journal of Current Advances in General Surgery

摘  要:目的:检测IL-17A、IL-10、IFN-γ在缓解期炎症性肠病(inflammatory bowl disease,IBD)患者中的表达,探讨诸炎症因子及Th17在炎症性肠病的发病及治疗中的作用。方法:应用ELISA检测12例Crohn病(Crohn disease,CD)、46例溃疡性结肠炎患者(ulcerative colitis,UC)和20例健康人(正常对照组)血清中IL-17A、IL-10和IFN-γ的水平,并用免疫组织化学法检测CD、UC及正常对照组结肠黏膜局部IL-17A的表达。结果:正常对照组结肠黏膜局部未检测到IL-17A的表达,而UC和CD组在结肠黏膜活组织中均检测到IL-17A的表达。同样UC和CD组血清中IL-17A明显增高,而正常对照组血清未检出IL-17A;UC和CD组患者血清IL-10水平均较对照组升高(P<0.05),且CD组明显高于UC组(P<0.05);CD、UC组与正常对照组血清中IFN-γ的表达差异无统计学意义(P>0.05)。结论:IL-17A不仅在缓解期IBD患者结肠黏膜局部表达,同时在其血清中高表达,提示Th17及其分泌的IL-17A在缓解期IBD患者的发病过程中起重要作用,并伴随促炎因子和抑炎性因子失调。Objective: To detect the expression of IL-17A,IL-10 and IFN-γ in patients wth different forms of inflammatory bowel disease (IBD) during clinical remission phase and investigate their role in the onset and treatment of IBD. Methods: Tissue samples were obtained from patients with ulcerative colitis (UC, n=46), Crohn's disease (CD, n=12), and normal colorectal tissues (n=20). IL-17A expression was evaluated by a standard immunohistochemical procedure. Serum IL-17A IL-10 and IFN-γ levels were determined by ELISA. Results: IL-17A expression was not detected in samples from normal colonic mucosa but was present in the mucosa of IBD. The level of IL-17A significantly increased in IBD patients while it was not detected in the sera of normal individuals. The level of IL-10 in patients with Crohn's disease was significantly higher than that in patients with ulcerative colitis and control group (P〈0.05 and P〈0.05, respectively). Conclusions: The expression of IL-17A in both the mucosa and serum of remission IBD patients increased significantly, the imbalance between production of proinflammatory and anti-inflammatory cytokines persisted even during remission of the disease.

关 键 词:结肠炎 溃疡性 CROHN病 白细胞介素17 白细胞介素10 

分 类 号:R574.62[医药卫生—消化系统]

 

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