首页> 外文期刊>Journal of Clinical Immunology >Dexamethasone-induced FKBP51 expression in peripheral blood mononuclear cells could play a role in predicting the response of asthmatics to treatment with corticosteroids.
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Dexamethasone-induced FKBP51 expression in peripheral blood mononuclear cells could play a role in predicting the response of asthmatics to treatment with corticosteroids.

机译:地塞米松诱导的FKBP51在外周血单个核细胞中的表达可能在预测哮喘患者对糖皮质激素治疗的反应中起一定作用。

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BACKGROUND: Corticosteroids (CSs) are the preferred anti-inflammatory therapy for the treatment of asthma, but the responses of asthmatics to CSs are known to vary. It has thus become important to discover reliable markers in predicting responses to CSs. METHODS: We performed time-series microarrays using a murine model of asthma after a single dose of dexamethasone, based on the assumption that the gene showing a greater change in response to CSs can also be a potential marker for that finding. We then evaluated the clinical meaning of the gene discovered in the microarray experiments. RESULTS: We found that the expression of FK506 binding protein 51 gene (FKBP51) in lung tissue markedly increased after dexamethasone treatment in a murine model of asthma. We then measured dexamethasone-induced FKBP51 expression in peripheral blood mononuclear cells (PBMCs) in asthmatics. Dexamethasone-induced FKBP51 expression in PBMCs was significantly higher in severe asthmatics compared with mild-to-moderate asthmatics treated with inhaled CSs. In addition, we found that dexamethasone-induced FKBP51 expression in PBMCs was inversely correlated with improvement in lung function after treatment with orally administered prednisolone in six steroid-naive asthmatics. CONCLUSION: Dexamethasone-induced FKBP51 expression in PBMCs may be a reliable and practical biomarker in predicting the response to CSs in asthmatics.
机译:背景:皮质类固醇(CSs)是治疗哮喘的首选抗炎疗法,但已知哮喘患者对CSs的反应有所不同。因此,在预测对CS的反应中发现可靠的标记就变得很重要。方法:我们基于在单次地塞米松治疗后哮喘的鼠模型进行了时间序列微阵列分析,其前提是该基因对CS的反应表现出更大的变化,也可能是该发现的潜在标志。然后,我们评估了在微阵列实验中发现的基因的临床意义。结果:我们发现,在哮喘小鼠模型中,地塞米松治疗后,肺组织中FK506结合蛋白51基因(FKBP51)的表达明显增加。然后,我们在哮喘患者中测量了地塞米松诱导的FKBP51在外周血单个核细胞(PBMC)中的表达。与吸入CSs治疗的轻度至中度哮喘患者相比,地塞米松诱导的PBMC中FKBP51表达明显高于重度哮喘患者。此外,我们发现,在六例未接受类固醇的哮喘患者中,口服泼尼松龙治疗后,地塞米松诱导的PBMC中FKBP51表达与肺功能改善呈负相关。结论:地塞米松诱导的PBMC中FKBP51表达可能是预测哮喘患者CS反应的可靠且实用的生物标志物。

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