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在致死性哮喘患者的气道中,表达糖皮质激素受体-β的细胞数量增加。

Increased number of glucocorticoid receptor-beta-expressing cells in the airways in fatal asthma.

作者信息

Christodoulopoulos P, Leung D Y, Elliott M W, Hogg J C, Muro S, Toda M, Laberge S, Hamid Q A

机构信息

Meakins-Christie Laboratories, McGill University, Montreal, Quebec, the University of British Columbia Pulmonary Research Laboratory, St Paul's Hospital, Vancouver, British Columbia, Canada.

出版信息

J Allergy Clin Immunol. 2000 Sep;106(3):479-84. doi: 10.1067/mai.2000.109054.

Abstract

BACKGROUND

We have recently demonstrated an increased number of glucocorticoid receptor-beta (GRbeta)-positive cells in steroid-insensitive subjects with severe asthma. Insensitivity to steroids may be a major contributing factor in fatal asthma; however, no such direct evidence has been report previously.

OBJECTIVE

Our aims were to investigate the expression of GRbeta immunoreactivity, an endogenous inhibitor of steroid action previously associated with steroid insensitivity, within the airways of patients who died of slow-onset fatal asthma and to compare its expression in patients with emphysema and in nonasthmatic subjects who died of unrelated causes. Sections from airways, both large and small, were obtained from 7 patients who died of asthma, 6 who died from emphysema, and 8 who died from nonpulmonary diseases. Sections from lungs of 6 patients with mild asthma whose lungs were resected for carcinoma were also included as controls.

METHODS

Tissue samples were processed for immunocytochemistry with a polyclonal antibody to GRbeta with use of the avidin-biotin technique and with monoclonal CD3, major basic protein, CD68, and elastase antibodies with the alkaline phosphatase-anti-alkaline phosphatase technique. Sequential immunocytochemistry was performed to phenotype the GRbeta immunoreactive cells. Tissue sections from both large (>2 mm) and small (<2 mm) airways were examined.

RESULTS

There was a significantly greater number of GRbeta immunoreactive cells in fatal asthma compared with emphysema and controls (P <.001 and P <.05, respectively). There was no difference in the expression of GRbeta in emphysema compared with controls. GRbeta immunoreactivity was also significantly higher in fatal asthma compared with mild asthma. The expression of GRbeta in the small airways of patients with severe asthma did not differ significantly from that in the large airways. The majority of GRbeta-positive cells were T cells and to a lesser extent eosinophils, macrophages, and neutrophils.

CONCLUSION

The results of this study support the association of GRbeta expression with fatal asthma and suggest that alternative anti-inflammatory agents need to be considered in the acute setting for patients who are not responding to steroid therapy.

摘要

背景

我们最近发现,在患有严重哮喘的类固醇不敏感患者中,糖皮质激素受体β(GRβ)阳性细胞数量增加。对类固醇不敏感可能是致死性哮喘的一个主要促成因素;然而,此前尚无此类直接证据的报道。

目的

我们的目的是研究GRβ免疫反应性(一种先前与类固醇不敏感相关的类固醇作用内源性抑制剂)在死于迟发性致死性哮喘患者气道中的表达情况,并将其在肺气肿患者以及死于非相关病因的非哮喘受试者中的表达进行比较。从7例死于哮喘的患者、6例死于肺气肿的患者以及8例死于非肺部疾病的患者身上获取了大小气道的切片。还纳入了6例因肺癌而切除肺部的轻度哮喘患者的肺组织切片作为对照。

方法

组织样本采用抗GRβ多克隆抗体,利用抗生物素蛋白-生物素技术进行免疫细胞化学处理,并采用碱性磷酸酶-抗碱性磷酸酶技术,使用单克隆CD3、主要碱性蛋白、CD68和弹性蛋白酶抗体进行处理。进行连续免疫细胞化学以对GRβ免疫反应性细胞进行表型分析。检查了大(>2毫米)小(<2毫米)气道的组织切片。

结果

与肺气肿和对照组相比,致死性哮喘中GRβ免疫反应性细胞数量显著更多(分别为P<.001和P<.05)。肺气肿与对照组相比,GRβ表达无差异。与轻度哮喘相比,致死性哮喘中GRβ免疫反应性也显著更高。重度哮喘患者小气道中GRβ的表达与大气道中的表达无显著差异。大多数GRβ阳性细胞是T细胞,嗜酸性粒细胞、巨噬细胞和中性粒细胞的比例较小。

结论

本研究结果支持GRβ表达与致死性哮喘之间的关联,并表明对于对类固醇治疗无反应的患者,在急性情况下需要考虑使用其他抗炎药物。

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