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首页> 外文期刊>Cytokine >Increased production of IL-1alpha and TNF-alpha in lipopolysaccharide-stimulated blood from obese patients with non-alcoholic fatty liver disease.
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Increased production of IL-1alpha and TNF-alpha in lipopolysaccharide-stimulated blood from obese patients with non-alcoholic fatty liver disease.

机译:肥胖非酒精性脂肪性肝病患者经脂多糖刺激的血液中IL-1α和TNF-α的产生增加。

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Enhanced pro-inflammatory cytokine production is considered a pathogenic factor in non-alcoholic fatty liver disease (NAFLD). Peripheral blood production of interleukin-1alpha (IL-1alpha) and tumor necrosis factor-alpha (TNF-alpha) was studied in relation to the severity of histological changes of the liver in obese NAFLD patients. Basal levels in serum and production of IL-1alpha and TNF-alpha in peripheral blood cell cultures after stimulation with lipopolysaccharide (enzyme-linked immunoabsorbent assays) were measured in 11 patients with steatosis and 15 with steatohepatitis, who underwent gastrectomy with a gastro-jejunal anastomosis in roux and Y, and in 9 controls who underwent anti-reflux surgery. Production of IL-1alpha and TNF-alpha was 122 and 67% higher in patients with steatosis than control values, respectively. In patients with steatohepatitis, IL-1alpha production was 300 and 80% higher and that of TNF-alpha 110 and 26% higher, as compared with controls and steatosis patients, respectively. Production of IL-1alpha was positively correlated with that of TNF-alpha (r=0.78, p<0.0001). IL-1alpha and TNF-alpha production were both positively correlated with the degree of steatosis (r=0.68, p<0.001 and r=0.74, p<0.0001) and steatohepatitis (r=0.77 and r=0.75, p<0.0001) at liver biopsy, and with the homeostasis model assessment index (r=0.73, p<0.0001 and r=0.63, p<0.01), respectively. Basal serum IL-1alpha and TNF-alpha levels were comparable in the three groups studied. It is concluded that elevated production of IL-1alpha and TNF-alpha by in vitro stimulated whole blood cell cultures occurs in NAFLD obese patients, which might play a pathophysiological role upon inflammatory leukocyte infiltration of the liver.
机译:促炎细胞因子产生的增加被认为是非酒精性脂肪肝疾病(NAFLD)的致病因素。研究了肥胖NAFLD患者肝脏白细胞介素1α(IL-1α)和肿瘤坏死因子-α(TNF-α)的外周血产生与肝脏组织学改变的严重性。在11例脂肪变性患者和15例脂肪性肝炎患者中,用脂多糖刺激(经胃空肠切除)后,测量血清的基础水平以及外周血细胞培养物中IL-1α和TNF-α的产生。肉瘤和Y以及其他9个接受抗反流手术的对照组进行了吻合术。脂肪变性患者的IL-1α和TNF-α产生分别比对照组高122和67%。与对照组和脂肪变性患者相比,在脂肪性肝炎患者中,IL-1α的产生分别高300和80%,TNF-α的产生高110和26%。 IL-1α的产生与TNF-α的产生呈正相关(r = 0.78,p <0.0001)。 IL-1α和TNF-α的产生均与脂肪变性程度(r = 0.68,p <0.001和r = 0.74,p <0.0001)和脂肪性肝炎(r = 0.77和r = 0.75,p <0.0001)呈正相关。肝活检和稳态模型评估指数(r = 0.73,p <0.0001,r = 0.63,p <0.01)。在研究的三组中基础血清IL-1α和TNF-α水平相当。结论是,在NAFLD肥胖患者中,通过体外刺激的全血细胞培养提高了IL-1α和TNF-α的产生,这可能在肝脏炎症性白细胞浸润中发挥了病理生理作用。

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