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囊性纤维化患者中白细胞介素-13表达增加,但白细胞介素-4未增加。

Increased expression of Interleukin-13 but not Interleukin-4 in cystic fibrosis patients.

作者信息

Hauber Hans-Peter, Gholami Djalal, Koppermann Gerhard, Heuer Hans-Eberhard, Meyer Andreas, Pforte Almuth

机构信息

Department of Internal Medicine, University Hospital Eppendorf, Germany.

出版信息

J Cyst Fibros. 2003 Dec;2(4):189-94. doi: 10.1016/S1569-1993(03)00091-2.

Abstract

BACKGROUND

Many patients with cystic fibrosis (CF) suffer from allergic disease, which can complicate treatment of CF lung disease. Interleukin (IL)-4 and IL-13 have been shown to be important mediators in allergic disease.

OBJECTIVE

To investigate the role of IL-4 and IL-13 in allergic and non-allergic CF patients.

METHODS

Expression of IL-4 and IL-13 mRNA was investigated in peripheral blood mononuclear cells (PBM) of seven CF patients with allergy, of six patients without allergy and of nine healthy subjects as well as in BAL cells of four patients and of all controls. PBM from six patients were incubated with recombinant human IL-13 or human antiIL-13 antibody without and with LPS stimulation and TNFalpha levels were measured by ELISA.

RESULTS

IL-13 mRNA expression was increased in allergic and non-allergic patients compared to controls. No significant difference in IL-4 expression could be found between patients and controls. Addition of IL-13 decreased TNFalpha in PBM culture supernatants.

CONCLUSION

Our data suggest that IL-13 rather than IL-4 might play an important role in both allergic and non-allergic CF patients. IL-13 might also compromise host defence by decreasing TNFalpha production.

摘要

背景

许多囊性纤维化(CF)患者患有过敏性疾病,这会使CF肺部疾病的治疗复杂化。白细胞介素(IL)-4和IL-13已被证明是过敏性疾病中的重要介质。

目的

研究IL-4和IL-13在过敏性和非过敏性CF患者中的作用。

方法

在7名有过敏症的CF患者、6名无过敏症的患者和9名健康受试者的外周血单核细胞(PBM)以及4名患者和所有对照的支气管肺泡灌洗(BAL)细胞中研究IL-4和IL-13 mRNA的表达。将6名患者的PBM与重组人IL-13或人抗IL-13抗体一起在有无LPS刺激的情况下孵育,并通过ELISA测量TNFα水平。

结果

与对照组相比,过敏性和非过敏性患者中IL-13 mRNA表达增加。患者和对照组之间在IL-4表达上未发现显著差异。添加IL-13可降低PBM培养上清液中的TNFα。

结论

我们的数据表明,IL-13而非IL-4可能在过敏性和非过敏性CF患者中均起重要作用。IL-13也可能通过降低TNFα的产生而损害宿主防御。

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