toll样受体7:一种用于溃疡性结肠炎缓解监测的新型非侵入性炎症基因传感器

Hamid Asadzadeh-Aghdaei, Leili Rejali, Mahyar Nourian, Vahid Chaleshi, Naghmeh Zamani, Shaghayegh Baradaran-Ghavami, Mohsen Nemati, Shabnam Shahrokh, Mohsen Norouzinia, Massoud Vosough, Ehsan Nazemalhosseini-Mojarad, Mohammadreza Zali
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引用次数: 0

摘要

背景:溃疡性结肠炎(UC)和克罗恩病(CD)是炎症性肠病(IBDs)的两种主要类型。toll样受体(TLRs)在先天免疫系统中表达,负责识别多种微生物。本研究的目的是评估TLR-2、-7和-8在UC患者外周血单个核细胞(PBMC)中的表达,作为一种新的无创原发性炎症传感器,用于监测UC候选人的临床病程。材料和方法:在这项横断面研究中,从42名UC患者和20名健康供体的PBMC中提取总RNA。采用实时定量聚合酶链反应(qRT-PCR)检测TLR-2、-7、-8 mRNA水平。结果:本研究表明,UC患者的TLR-2 mRNA表达与对照组相比没有显著变化(P = 0.1264),而UC参与者的TLR-7表达在缓解过程中与健康供者和发作患者相比有显著升高(P = 0.0008) (P = 0.0004和P = 0.0063)。最后选择的TLR, TLR-8在UC患者和对照组之间或在疾病的临床病程之间均未显示显着变化。结论:在三种被提名的预测UC患者的tlr中,TLR-7可能是根据急性UC患者和对照供者mRNA表达的显著差异而被选择的。TLR-7可以作为一种新的无创生物标志物,用于监测UC患者的活动性病程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Toll-Like Receptor 7 a Novel Non-Invasive Inflammatory Genetic Sensor for Ulcerative Colitis Remission Monitoring.

Toll-Like Receptor 7 a Novel Non-Invasive Inflammatory Genetic Sensor for Ulcerative Colitis Remission Monitoring.

Toll-Like Receptor 7 a Novel Non-Invasive Inflammatory Genetic Sensor for Ulcerative Colitis Remission Monitoring.

Toll-Like Receptor 7 a Novel Non-Invasive Inflammatory Genetic Sensor for Ulcerative Colitis Remission Monitoring.

Background: Ulcerative colitis (UC) and Crohn's disease (CD) are two major types of inflammatory bowel diseases (IBDs). Toll-like receptors (TLRs) are expressed in the innate immune system compartments, in charge of identifying a wide range of microorganisms. The aim of the present study was to evaluate the expression of TLR-2, -7, and -8 in peripheral blood mononuclear cells (PBMC) of UC patients as a novel non-invasive primary inflammation sensor for monitoring the clinical course of UC candidates.

Materials and methods: In this cross-sectional study, total RNA was extracted from the PBMC of 42 UC patients along with 20 healthy donors. The mRNA levels of TLR-2, -7, and -8 were assessed using the quantitative real-time polymerase chain (qRT-PCR) reaction.

Results: The present research study demonstrated no significant changes in TLR-2 mRNA expression in UC patients in comparison with the control group (P = 0.1264), whereas significant elevation (P = 0.0008) was distinguished in the TLR-7 expression of UC participants specifically during the remission course compared with healthy donors and flareup patients (P = 0.0004 and P = 0.0063, respectively). The last selected TLR, TLR-8 was not shown remarkable changes either between UC patients and the control group or between clinical courses of the disease.

Conclusion: Here, among three nominated TLRs for predicting UC patients, TLR-7 was potentially selected according to the significant difference in mRNA expression in flareup UC patients and control donors. TLR-7 could be used as a novel non-invasive biomarker for monitoring UC patients in the active course of the disease.

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