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Intestinal cytokine gene expression in infants with acute necrotizing enterocolitis: interleukin-11 mRNA expression inversely correlates with extent of disease.

机译:急性坏死性小肠结肠炎婴儿的肠道细胞因子基因表达:白细胞介素11 mRNA表达与疾病程度呈负相关。

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BACKGROUND/PURPOSE: The authors have shown previously that surgical specimens from infants with acute necrotizing enterocolitis (NEC) show upregulation of inducible nitric oxide (NO) synthase (iNOS) and interferon-gamma mRNA. However, the contribution of other inflammatory cytokines such as interleukin-8 (IL-8), IL-11, and IL-12 has not been defined. Likewise, the role of GTP-cyclohydrolase, the rate-limiting enzyme in tetrahydrobiopterin synthesis, and thus NO production by iNOS is unclear. In this study, the authors sought to further define the pattern of cytokine expression seen in infants with acute NEC. METHODS: The authors measured intestinal cytokine mRNA expression by semiquantitative reverse transcriptase polymerase chain reaction in 21 infants with histologically confirmed NEC, 18 with other inflammatory conditions, and in 9 patients without intestinal inflammation. Guanosine triphosphate-cyclohydrolase (GTP-CH) activity was measured by specific enzyme assay. Univariate exact logistic regression analysis was performed to identify predictors of outcome. RESULTS: IL-8 and IL-11 mRNA were upregulated in patients with acute NEC compared with those with other inflammatory conditions or those without disease; these levels returned to baseline at the time of stoma closure. Increased IL-11 mRNA decreased the likelihood of pan-necrosis (odds ratio, 0.93; P =.002). Increased IL-12 levels (but not IL-8) seemed to protect against pan-necrosis (odds ratio, 0.70; P =.06). CONCLUSIONS: Local upregulation of IL-11 may represent an adaptive response designed to limit the extent of intestinal damage in NEC. Decreased IL-12 levels may contribute to the pathogenesis of NEC by allowing bacteria to escape host defenses. Copyright 2001 by W.B. Saunders Company.
机译:背景/目的:作者先前已经表明,来自患有急性坏死性小肠结肠炎(NEC)的婴儿的手术标本显示出诱导型一氧化氮(NO)合酶(iNOS)和干扰素-γmRNA的上调。但是,尚未确定其他炎性细胞因子如白介素8(IL-8),IL-11和IL-12的作用。同样,GTP-环水解酶(四氢生物蝶呤合成中的限速酶)的作用尚不清楚,因此iNOS不会产生NO。在这项研究中,作者试图进一步定义在急性NEC婴儿中看到的细胞因子表达模式。方法:作者通过半定量逆转录酶聚合酶链反应检测了21例经组织学证实为NEC的婴儿,18例患有其他炎症的婴儿和9例无肠道炎症的婴儿的肠道细胞因子mRNA表达。鸟苷三磷酸环水解酶(GTP-CH)活性通过特异性酶法测定。进行单变量精确逻辑回归分析以鉴定结果的预测因子。结果:与其他炎症性疾病或无疾病的患者相比,急性NEC患者的IL-8和IL-11 mRNA表达上调。这些水平在造口闭合时恢复到基线。 IL-11 mRNA的增加降低了泛坏死的可能性(比值比为0.93; P = 0.002)。 IL-12水平升高(而非IL-8水平升高)似乎可以预防泛坏死(优势比为0.70; P = .06)。结论:IL-11的局部上调可能代表一种适应性反应,旨在限制NEC肠道损伤的程度。 IL-12水平的降低可能通过使细菌逃脱宿主防御而导致NEC的发病。 W.B.版权所有2001桑德斯公司。

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