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内毒素暴露下人呼吸道中的白细胞介素-17 产生 T 辅助细胞及相关细胞因子。

Interleukin-17-producing T-helper cells and related cytokines in human airways exposed to endotoxin.

机构信息

Lung Immunology Group Dept of Internal Medicine/Respiratory Medicine and Allergology Sahlgrenska Academy, University of Gothenburg, Box 480, SE 405 30 Gothenburg, Sweden.

出版信息

Eur Respir J. 2010 Nov;36(5):1155-64. doi: 10.1183/09031936.00170609. Epub 2010 Feb 25.

DOI:10.1183/09031936.00170609
PMID:20185422
Abstract

Previous studies on mouse models have indicated that interleukin (IL)-17 and IL-17-producing T-helper (Th) cells are important for pulmonary host defence against Gram-negative bacteria. Human correlates to these findings have not yet been demonstrated. The aim of the present study was to determine whether or not IL-17-producing Th cells are present and whether IL-17 and other Th17-associated cytokines are involved in the immunological response to endotoxin in human airways. Segmental exposure to endotoxin and contralateral exposure to vehicle were performed in the lungs of healthy volunteers, with subsequent bronchoalveolar lavage 12 or 24 h after exposure to study local changes in cytokines and inflammatory cells. Endotoxin exposure increased concentrations of IL-17, IL-22 and their downstream effector molecules, human β-defensin-2 and IL-8/CXC chemokine ligand 8, in bronchoalveolar lavage fluid. Th cells with the capacity to produce IL-17 were found among the bronchoalveolar lavage cells, and expression of IL-17 mRNA correlated with expression of the transcription factor, retinoic-acid-receptor-related orphan receptor C variant 2. Moreover, endotoxin increased the numbers of neutrophils, macrophages and IL-17-producing T-cells, as well as the concentration of the Th17-regulating cytokines, IL-21 and IL-23. In conclusion, IL-17-producing Th cells are present, and IL-17, as well as other Th17-associated cytokines, is involved in the immunological response to endotoxin in human airways.

摘要

先前在小鼠模型上的研究表明,白细胞介素(IL)-17 和产生 IL-17 的辅助性 T 细胞(Th)对于肺部防御革兰氏阴性细菌至关重要。但这些发现尚未在人体中得到证实。本研究旨在确定是否存在产生 IL-17 的 Th 细胞,以及 IL-17 和其他 Th17 相关细胞因子是否参与了人体气道对内毒素的免疫反应。在健康志愿者的肺部进行节段性内毒素暴露和对侧载体暴露,在暴露后 12 或 24 小时进行支气管肺泡灌洗,以研究局部细胞因子和炎症细胞的变化。内毒素暴露增加了支气管肺泡灌洗液中 IL-17、IL-22 及其下游效应分子、人β防御素-2 和 IL-8/CXC 趋化因子配体 8 的浓度。在支气管肺泡灌洗液中发现了具有产生 IL-17 能力的 Th 细胞,并且 IL-17 mRNA 的表达与转录因子视黄酸受体相关孤儿受体 C 变体 2 的表达相关。此外,内毒素增加了中性粒细胞、巨噬细胞和产生 IL-17 的 T 细胞的数量,以及 Th17 调节细胞因子 IL-21 和 IL-23 的浓度。总之,存在产生 IL-17 的 Th 细胞,IL-17 以及其他 Th17 相关细胞因子参与了人体气道对内毒素的免疫反应。

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