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炎症性肠病患者T淋巴细胞亚群的改变及临床意义 被引量:17

Clinical Significance of T-Lymphocyte Subsets Changes in Inflammatory Bowel Disease
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摘要 目的:探讨炎症性肠病(IBD)患者外周血T淋巴细胞亚群的变化特点及临床意义。方法:对临床确诊的18例溃疡性结肠炎(UC)和9例Crohn病(CD)患者,于疾病的不同时期用荧光单克隆抗体标记一流式细胞仪技术检测其外周血T淋巴细胞亚群的变化,并结合临床和病理资料进行综合分析。结果:UC患者缓解期时的CD3+、CD8+和自然杀伤(NK)细胞与对照组比较无显著差异;但活动期时,其CD8+和NK细胞数明显下降(CD8+:活动期:23.1%±1.0%,对照组:31.3%±1.2%,P<0.05;NK:活动期:9.8%±1.0%,对照组:15.1%±1.1%,P<0.01),CD4+/CD8+比值上升(活动期:1.8±0.1,对照组:1.4±0.02,P<0.05);活动期CD患者的CD8+细胞和CD4+/CD8+比值(43.0%±4.4%和0.6±0.1)变化却与UC组活动期呈相反趋势(P<0.01)。结论:T淋巴细胞亚群改变在IBD的发病机制中可能起重要作用;UC和CD的细胞免疫机制不同;外周血CD4+、CD8+、NK细胞和CD4+/CD8+比值可作为检测UC病情变化和疗效考核的敏感指标。 Background/Aims: To investigate the changes and clinical significance of peripheral blood T-lym- phocyte subsets in patients with inflammatory bowel disease (IBD) during various stages. Methods: 18 patients with ulcerative colitis (UC), 9 with Crohn disease (CD) and 10 normal volunteers were re- cruited in this study. The T-lymphocyte subsets were investigated by immunofluorescence flow cyto- metry analysis and analyzed with clinical activity index. Results: Compared with controls, no signifi- cant difference in CD3+, CD8+ and natural killer (NK) cells were observed in inactive stage of UC. But in active stage of UC, CD8+ and NK cells decreased significantly (CD8+: 23.1%±1.0% vs 31.3%±1.2%, P<0.05;NK:9.8%±1.0% vs 15.1% ± .1%, P< 0.01), and CD.+/CD,+ ratio increased (1.8t0.1 vs 1.4t 0.02, P<0.05). The changes of CD,+ and CD,+/CD,+ ratio in active stage of CD were contrary to those o f UC in the active stage (P<0.01). Conclusions: Alteration of T-lymphocyte subsets may contribute to the pathogenesis of active UC inflammation. The disorders of T-lymphocyte subsets may play dif- ferent role in UC and CD. The number of CD4+, CD8+, NK cells and CD4+/CD8+ ratio may be valuable in monitoring the disease stages and in guidance of treatment.
出处 《胃肠病学》 2000年第4期220-222,共3页 Chinese Journal of Gastroenterology
关键词 溃疡性结肠炎 T淋巴细胞亚群 CD4阳性T淋巴细胞 CD8阳性T淋巴细胞 Colitis, Ulcerative T-Lymphocyte Subsets CD4-Positive T-Lymphocytes CD8-Positive T-Lymphocytes
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