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[黏膜β-防御素-2、肿瘤坏死因子α及白细胞介素-1β在溃疡性结肠炎中的表达及意义]

[Expression and significance of mucosal beta-defensin-2, TNFalpha and IL-1beta in ulcerative colitis].

作者信息

Chang Yu-Ying, Ouyang Qin

机构信息

Department of Gastroenterology, West China Hospital of Sichuan University, Chengdu 610041, China.

出版信息

Zhonghua Nei Ke Za Zhi. 2008 Jan;47(1):11-4.

Abstract

OBJECTIVE

To investigate the expression and significance of human beta-defensin-2 (HBD2), TNFalpha and IL-1beta in ulcerative colitis (UC).

METHODS

Thirty-five patients with active UC diagnosed by the department of gastroenterology in West China Hospital were included in this study. Ulcerative colitis disease activity index (UCAI) was assessed and the pathological grades of UC were classified. Immunohistochemistry assay and real-time quantitative PCR were used for the expression of HBD2, TNFalpha, IL-1beta in colonic mucosa of UC.

RESULTS

Among the 35 patients with UC, 10 cases were mild, 13 moderate and 12 severe. Of the 35 cases, there were 11 with grade I, 13 grade II and 11 grade III lesion according to Truelove criteria. The score of UCAI had positive correlation with pathological grading (r = 0.890, P < 0.01). The expressions of HBD2, TNFalpha, IL-1beta in colonic mucosa of UC with immunohistochemistry and real-time quantitative PCR were significantly higher than those in healthy control (P < 0.05); the expressions increased gradually with the severity of pathological grade and there was a higher expression of them in inflamed area than in non-inflamed (P < 0.05). A good positive correlation was also found between HBD2 and other inflammatory cytokines.

CONCLUSIONS

It is shown that there is a higher expression of HBD2 in colonic mucosa as compared with healthy control, a higher expression of it in inflamed area than in non-inflamed area and a positive correlation of expression between HBD2 and pro-inflammatory cytokines such as TNFalpha and IL-1beta, implying that HBD2 and pro-inflammatory cytokines are interdependent and interactive playing an important role in magnifying and aggravating inflammatory injury in UC.

摘要

目的

探讨人β-防御素-2(HBD2)、肿瘤坏死因子α(TNFα)和白细胞介素-1β(IL-1β)在溃疡性结肠炎(UC)中的表达及意义。

方法

纳入四川大学华西医院胃肠病科确诊的35例活动期UC患者。评估溃疡性结肠炎疾病活动指数(UCAI),并对UC进行病理分级。采用免疫组织化学法和实时定量PCR检测UC结肠黏膜中HBD2、TNFα、IL-1β的表达。

结果

35例UC患者中,轻度10例,中度13例,重度12例。根据Truelove标准,35例中I级病变11例,II级病变13例,III级病变11例。UCAI评分与病理分级呈正相关(r = 0.890,P < 0.01)。免疫组织化学法和实时定量PCR检测显示,UC结肠黏膜中HBD2、TNFα、IL-1β的表达明显高于健康对照(P < 0.05);其表达随病理分级的加重而逐渐升高,且炎症区域的表达高于非炎症区域(P < 0.05)。HBD2与其他炎性细胞因子之间也存在良好的正相关。

结论

结果表明,与健康对照相比,UC结肠黏膜中HBD2表达较高,炎症区域的表达高于非炎症区域,且HBD2与TNFα和IL-1β等促炎细胞因子的表达呈正相关,这意味着HBD2与促炎细胞因子相互依存、相互作用,在UC炎症损伤的放大和加重中起重要作用。

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