首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Altered Th1/Th2 cytokine profiles in the intestinal mucosa of patients with inflammatory bowel disease as assessed by quantitative reversed transcribed polymerase chain reaction (RT-PCR).
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Altered Th1/Th2 cytokine profiles in the intestinal mucosa of patients with inflammatory bowel disease as assessed by quantitative reversed transcribed polymerase chain reaction (RT-PCR).

机译:通过定量逆转录聚合酶链反应(RT-PCR)评估炎症性肠病患者肠粘膜中Th1 / Th2细胞因子的改变。

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摘要

Cytokines serve a central function as key factors in the regulation of the intestinal immune response and mediation of tissue damage in inflammatory bowel disease (IBD). Abnormalities in the expression of immunoregulatory cytokines such as IL-2, IL-4, IL-10 and interferon-gamma (IFN-gamma) may indicate a dysregulation of intestinal immunity probably associated with pathogenic events. Therefore, cytokine mRNA concentrations were determined in the mucosa of patients with IBD at sites of active (n = 13) and inactive (n = 12) ulcerative colitis (UC), active (n = 11) and inactive (n = 11) Crohn's disease (CD) and in control patients (n = 14) using quantitative RT-PCR. IL-10 mRNA concentrations were significantly increased in patients with both active UC (P < 0.001) and active CD (P < 0.005) compared with control patients. IFN-gamma mRNA concentrations were also significantly increased both in patients with active UC (P < 0.02) and active CD (P < 0.05) compared with control patients, whereas IL-2 mRNA levels were significantly (P < 0.02) increased only in active CD. IL-4 mRNA expression in the intestinal mucosa was frequently below the detection limit. Our results demonstrate that chronic intestinal inflammation in patients with CD is characterized by an increase of Th1-like cytokines. Furthermore, the increased IL-10 mRNA expression at sites of active IBD suggests that IL-10 is an important regulatory component involved in the control of the inflammatory response in inflammatory bowel disease.
机译:细胞因子在炎症性肠病(IBD)中的肠道免疫反应调节和组织损伤的调节中起着关键作用。免疫调节细胞因子如IL-2,IL-4,IL-10和干扰素-γ(IFN-γ)的表达异常可能表明肠道免疫失调可能与病原体事件有关。因此,在活动性(n = 13)和非活动性(n = 12)溃疡性结肠炎(UC),活动性(n = 11)和非活动性(n = 11)克罗恩氏病患者的IBD患者的粘膜中确定了细胞因子mRNA的浓度。疾病(CD)和对照组(n = 14)使用定量RT-PCR。与对照组相比,活动性UC(P <0.001)和活动性CD(P <0.005)患者的IL-10 mRNA浓度均显着增加。与对照组相比,活动性UC(P <0.02)和活动性CD(P <0.05)患者的IFN-γmRNA浓度也显着升高,而IL-2 mRNA水平仅显着升高(P <0.02)。光盘。肠粘膜中IL-4 mRNA的表达经常低于检测极限。我们的结果表明,CD患者的慢性肠道炎症的特征在于Th1样细胞因子的增加。此外,在活性IBD位点的IL-10 mRNA表达增加表明IL-10是参与控制炎症性肠病中炎症反应的重要调节成分。

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