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创伤后嗜酸性粒细胞性胸腔积液中的白细胞介素-5

IL-5 in post-traumatic eosinophilic pleural effusion.

作者信息

Schandené L, Namias B, Crusiaux A, Lybin M, Devos R, Velu T, Capel P, Bellens R, Goldman M

机构信息

Department of Immunology-Haematology, Hôpital Erasme, Université Libre de Bruxelles, Belgium.

出版信息

Clin Exp Immunol. 1993 Jul;93(1):115-9. doi: 10.1111/j.1365-2249.1993.tb06506.x.

Abstract

Thoracic trauma or pneumothorax can result in pleural fluid eosinophilia. In this study we investigated the role of the eosinophilopoietic cytokine IL-5 in three cases of post-traumatic eosinophilic pleural effusions (EPE). Using a specific immunoenzymatic assay, significant levels of IL-5 were found in EPE (range 100-3000 pg/ml), while IL-5 was undetectable (< 25 pg/ml) in corresponding serum samples and in non-eosinophilic pleural fluids. IL-5 present in pleural fluids was found bioactive in a proliferative assay using a mouse CTLL-2 cell line transfected with the cDNA corresponding to the alpha chain of the human IL-5 receptor. Using a reverse polymerase chain reaction (PCR) method, we found IL-5 mRNA expression within pleural mononuclear cells from patients with EPE, but not in corresponding peripheral blood mononuclear cells (PBMC), confirming that IL-5 is synthesized locally in the pleural cavity. In the two cases in which pleural CD4+ cells were purified, these cells were identified as the major source of IL-5. Taken together, these data indicate that the development of post-traumatic EPE is related to a local secretion of IL-5 by CD4+ cells present in the pleural cavity.

摘要

胸部创伤或气胸可导致胸腔积液嗜酸性粒细胞增多。在本研究中,我们调查了嗜酸性粒细胞生成细胞因子白细胞介素-5(IL-5)在3例创伤后嗜酸性胸腔积液(EPE)中的作用。采用特异性免疫酶测定法,在EPE中发现了显著水平的IL-5(范围为100 - 3000 pg/ml),而在相应的血清样本和非嗜酸性胸腔积液中未检测到IL-5(< 25 pg/ml)。在使用转染了与人IL-5受体α链对应的cDNA的小鼠CTLL-2细胞系进行的增殖试验中,发现胸腔积液中存在的IL-5具有生物活性。使用逆转录聚合酶链反应(PCR)方法,我们在EPE患者的胸腔单核细胞中发现了IL-5 mRNA表达,但在相应的外周血单核细胞(PBMC)中未发现,这证实IL-5是在胸腔内局部合成的。在2例纯化了胸腔CD4 +细胞的病例中,这些细胞被确定为IL-5的主要来源。综上所述,这些数据表明创伤后EPE的发生与胸腔内存在的CD4 +细胞局部分泌IL-5有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ba2/1554754/4728c9c19282/clinexpimmunol00032-0119-a.jpg

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