...
首页> 外文期刊>Thorax: The Journal of the British Thoracic Society >Relative corticosteroid insensitivity of alveolar macrophages in severe asthma compared with non-severe asthma.
【24h】

Relative corticosteroid insensitivity of alveolar macrophages in severe asthma compared with non-severe asthma.

机译:与非严重哮喘相比,重度哮喘患者肺泡巨噬细胞相对于皮质类固醇不敏感。

获取原文
获取原文并翻译 | 示例

摘要

BACKGROUND: About 5-10% of patients with asthma suffer from poorly controlled disease despite corticosteroid (CS) treatment, which may indicate the presence of CS insensitivity. A study was undertaken to determine whether relative CS insensitivity is present in alveolar macrophages from patients with severe asthma and its association with p38 mitogen-activated protein kinase (MAPK) activation and MAPK phosphatase-1 (MKP-1). METHODS: Fibreoptic bronchoscopy and bronchoalveolar lavage (BAL) were performed in 20 patients with severe asthma and 19 with non-severe asthma and, for comparison, in 14 normal volunteers. Alveolar macrophages were exposed to lipopolysaccharide (LPS, 10 mug/ml) and dexamethasone (10(-8) and 10(-6) M). Supernatants were assayed for cytokines using an ELISA-based method. p38 MAPK activity and MKP-1 messenger RNA expression were assayed in cell extracts. RESULTS: The inhibition of LPS-induced interleukin (IL)1beta, IL6, IL8, monocyte chemotactic protein (MCP)-1 and macrophage inflammatory protein (MIP)-1alpha release by dexamethasone (10(-6) M) was significantly less in macrophages from patients with severe asthma than in macrophages from patients with non-severe asthma. There was increased p38 MAPK activation in macrophages from patients with severe asthma. MKP-1 expression induced by dexamethasone and LPS, expressed as a ratio of LPS-induced expression, was reduced in severe asthma. CONCLUSION: Alveolar macrophages from patients with severe asthma demonstrate CS insensitivity associated with increased p38 MAPK activation that may result from impaired inducibility of MKP-1.
机译:背景:尽管有皮质类固醇(CS)治疗,约有5-10%的哮喘患者疾病控制不佳,这可能表明存在CS不敏感性。进行了一项研究,以确定患有严重哮喘的患者的肺泡巨噬细胞中是否存在相对CS不敏感性及其与p38丝裂原活化蛋白激酶(MAPK)活化和MAPK磷酸酶-1(MKP-1)的关系。方法:对20例重度哮喘患者和19例非重度哮喘患者进行了纤维支气管镜检查和支气管肺泡灌洗(BAL),并比较了14名正常志愿者。肺泡巨噬细胞暴露于脂多糖(LPS,10杯/毫升)和地塞米松(10(-8)和10(-6)M)。使用基于ELISA的方法分析上清液中的细胞因子。在细胞提取物中测定p38 MAPK活性和MKP-1信使RNA表达。结果:地塞米松(10(-6)M)对LPS诱导的白介素(IL)1beta,IL6,IL8,单核细胞趋化蛋白(MCP)-1和巨噬细胞炎性蛋白(MIP)-1alpha释放的抑制作用明显降低。严重哮喘患者的巨噬细胞比非严重哮喘患者的巨噬细胞高。重症哮喘患者巨噬细胞中p38 MAPK激活增加。在严重哮喘中,地塞米松和LPS诱导的MKP-1表达降低,以LPS诱导表达的比例表示。结论:重度哮喘患者的肺泡巨噬细胞显示CS不敏感与p38 MAPK活化增加有关,这可能是由于MKP-1的诱导能力受损所致。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号