{"title":"Protective effect of TSLP and IL-33 cytokines in ulcerative colitis.","authors":"Sahar Tahaghoghi-Hajghorbani, Abolghasem Ajami, Saeedeh Ghorbanalipoor, Zahra Hosseini-Khah, Saeid Taghiloo, Peyman Khaje-Enayati, Vahid Hosseini","doi":"10.1186/s13317-019-0110-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Inflammatory bowel disease (IBD) primarily includes ulcerative colitis (UC) and Crohn's disease (CD). Thymic stromal lymphopoietin (TSLP) is a cytokine produced by intestinal epithelial cells (IECs) with immunomodulatory properties that plays an important role in the development of regulatory T cell (Treg) responses and tolerance in the gut. On the other hand, IL-33 has been considered as a cytokine with two different properties, inflammatory and anti-inflammatory functions, the latter may play a protective role against chronic intestinal inflammation. In the present study, we investigated the relative gene expression levels of TSLP and IL-33 molecules in ulcerative colitis.</p><p><strong>Methods: </strong>Patients with clinical symptoms of colitis undergoing a routine diagnostic colonoscopy were included in this study. Biopsy specimens were collected and divided into two parts. One part was fixed and processed for routine histopathological examinations and the other part was stored for RNA extraction. TSLP and IL-33 gene expression were determined using the SYBR Green qRT-PCR.</p><p><strong>Results: </strong>The expression level of TSLP and IL-33 were significantly lower in UC patients compared with the control group. Moreover, the expressions of these cytokines were more down-regulated in severe UC patients compared with mild and moderate ones and the control group. We also showed a positive correlation between low expression of TSLP and IL-33 and the severity of UC disease.</p><p><strong>Conclusions: </strong>In this study, we showed decreased mRNA expression levels of TSLP and IL-33 in UC patients and also a negative correlation between expression of TSLP and IL-33 and severity of UC disease.</p>","PeriodicalId":8655,"journal":{"name":"Auto-Immunity Highlights","volume":"10 1","pages":"1"},"PeriodicalIF":0.0000,"publicationDate":"2019-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s13317-019-0110-z","citationCount":"17","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Auto-Immunity Highlights","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s13317-019-0110-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 17
Abstract
Purpose: Inflammatory bowel disease (IBD) primarily includes ulcerative colitis (UC) and Crohn's disease (CD). Thymic stromal lymphopoietin (TSLP) is a cytokine produced by intestinal epithelial cells (IECs) with immunomodulatory properties that plays an important role in the development of regulatory T cell (Treg) responses and tolerance in the gut. On the other hand, IL-33 has been considered as a cytokine with two different properties, inflammatory and anti-inflammatory functions, the latter may play a protective role against chronic intestinal inflammation. In the present study, we investigated the relative gene expression levels of TSLP and IL-33 molecules in ulcerative colitis.
Methods: Patients with clinical symptoms of colitis undergoing a routine diagnostic colonoscopy were included in this study. Biopsy specimens were collected and divided into two parts. One part was fixed and processed for routine histopathological examinations and the other part was stored for RNA extraction. TSLP and IL-33 gene expression were determined using the SYBR Green qRT-PCR.
Results: The expression level of TSLP and IL-33 were significantly lower in UC patients compared with the control group. Moreover, the expressions of these cytokines were more down-regulated in severe UC patients compared with mild and moderate ones and the control group. We also showed a positive correlation between low expression of TSLP and IL-33 and the severity of UC disease.
Conclusions: In this study, we showed decreased mRNA expression levels of TSLP and IL-33 in UC patients and also a negative correlation between expression of TSLP and IL-33 and severity of UC disease.
目的:炎症性肠病(IBD)主要包括溃疡性结肠炎(UC)和克罗恩病(CD)。胸腺基质淋巴生成素(TSLP)是一种由肠上皮细胞(IECs)产生的具有免疫调节特性的细胞因子,在肠道调节性T细胞(Treg)反应和耐受的发展中起重要作用。另一方面,IL-33被认为是一种具有炎症和抗炎两种不同特性的细胞因子,后者可能对慢性肠道炎症起保护作用。在本研究中,我们研究了TSLP和IL-33分子在溃疡性结肠炎中的相对基因表达水平。方法:有结肠炎临床症状的患者行常规结肠镜检查。采集活检标本,分为两部分。一部分固定处理用于常规组织病理学检查,另一部分保存用于RNA提取。采用SYBR Green qRT-PCR检测TSLP和IL-33基因的表达。结果:UC患者TSLP、IL-33表达水平明显低于对照组。与轻、中度UC患者及对照组相比,这些细胞因子在重度UC患者中的表达下调更明显。我们还发现TSLP和IL-33的低表达与UC疾病的严重程度呈正相关。结论:在本研究中,我们发现UC患者TSLP和IL-33 mRNA表达水平降低,且TSLP和IL-33表达与UC疾病严重程度呈负相关。