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在轻症和重症急性胰腺炎期间细胞因子表达的不同谱。

Different profiles of cytokine expression during mild and severe acute pancreatitis.

机构信息

Laboratory for Research of Digestive System, Institute for Biomedical Research, Eiveniu Str. 2, 50009 Kaunas, Lithuania.

出版信息

World J Gastroenterol. 2010 Apr 21;16(15):1845-53. doi: 10.3748/wjg.v16.i15.1845.

Abstract

AIM

To study secretion patterns of pro- and anti-inflammatory cytokines, and activation of various cellular subsets of leukocytes in peripheral blood.

METHODS

We have conducted a prospective observational study. One hundred and eight patients with a diagnosis of acute pancreatitis and onset of the disease within last 72 h were included in this study. The mRNA expression of 25 different types of cytokines in white blood cells was determined by quantitative real time polymerase chain reaction. Levels of 8 different cytokines in blood serum were measured by enzyme linked immunosorbent assay. Clinical data and cytokine expression results were subjected to statistical analysis.

RESULTS

Severe and necrotizing acute pancreatitis (AP) is characterized by the significant depletion of circulating lymphocytes. Severe acute pancreatitis is associated with a typical systemic inflammatory response syndrome and over-expression of pro-inflammatory cytokines [interleukin (IL)-6, IL-8, macrophage migration inhibitory factor (MIF)]. Serum IL-6 and MIF concentrations are the best discriminators of severe and necrotizing AP as well as possible fatal outcome during the early course of the disease.

CONCLUSION

Deregulation of cellular immune system is a key event leading to severe and necrotizing AP. IL-6 and MIF could be used as early predictors of complications.

摘要

目的

研究前炎症细胞因子和后炎症细胞因子的分泌模式,以及外周血中白细胞各细胞亚群的激活情况。

方法

我们进行了一项前瞻性观察性研究。纳入了 108 例在发病后 72 小时内确诊为急性胰腺炎的患者。通过实时定量聚合酶链反应(PCR)测定白细胞中 25 种不同类型细胞因子的 mRNA 表达,采用酶联免疫吸附试验(ELISA)测定血清中 8 种不同细胞因子的水平。对临床数据和细胞因子表达结果进行统计学分析。

结果

严重和坏死性急性胰腺炎(AP)的特征是循环淋巴细胞大量减少。严重急性胰腺炎与典型的全身炎症反应综合征和前炎症细胞因子(白细胞介素(IL)-6、IL-8、巨噬细胞移动抑制因子(MIF))过度表达有关。血清 IL-6 和 MIF 浓度是区分严重和坏死性 AP 以及疾病早期可能发生致命后果的最佳指标。

结论

细胞免疫系统失调是导致严重和坏死性 AP 的关键事件。IL-6 和 MIF 可作为并发症的早期预测指标。

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