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肺泡蛋白沉积症样改变在特发性间质性肺炎中的特征表现为 club 细胞丢失。

Club Cell Loss as a Feature of Bronchiolization in ILD.

机构信息

Department of Respiratory Diseases, Univ Montpellier, CHU Montpellier, Montpellier, France.

PhyMedExp, Univ Montpellier, CNRS, INSERM, CHU Montpellier, Montpellier, France.

出版信息

Front Immunol. 2021 Feb 26;12:630096. doi: 10.3389/fimmu.2021.630096. eCollection 2021.

Abstract

Distal airway metaplasia may precede honeycombing in progressive fibrosing interstitial lung disease (ILD). The SCGB1A1 bronchiolar-specific club cell may play a role in this aberrant regenerative process. To assess the presence of club cells in the small airways of patients suffering from ILD. Small airways (internal diameter <2 mm) in lung samples [surgical lung biopsy (SLB) and/or transbronchial lung cryobiopsy (TBLC)] from 14 patients suffering from ILD and 10 controls were morphologically assessed and stained for SCGB1A1. SCGB1A1 was weighted by epithelial height as a marker of airway generation (SCGB1A1/EH). Correlations between clinical, functional, and high-resolution CT (HRCT) prognostic factors and histomorphometry were assessed. Small airways from samples with ILD patterns were significantly less dense in terms of SCGB1A1 cells [0.064 (0.020-0.172)] as compared to controls' sample's small airways [0.393 (0.082-0.698), < 0.0001]. Usual interstitial pneumonia (UIP) patterns most frequently contained small airways with limited or absent SCGB1A1 expression (SCGB1A1/EH <0.025): UIP (18/33; 55%) as compared with non-UIP patterns (4/31; 13%) or controls (0/29; 0%): < 0.0001. In addition, correlations with HRCT indicated a significant negative relationship between SCGB1A1 and bronchiectasis as a feature of bronchiolization (Rho -0.63, < 0.001) and a positive relationship with both forced vital capacity (FVC) and Hounsfield unit (HU)-distribution pattern in kurtosis (Rho 0.38 and 0.50, respectively, both < 0.001) as markers of fibrotic changes. Compared with controls, the small airways of patients with ILD more often lack SCGB1A1, especially so in UIP. Low densities of SCGB1A1-marked cells correlate with bronchiectasis and fibrotic changes. Further research investigating SCGB1A1 staining as a pathological feature of the bronchiolization process is merited.

摘要

远端气道化生可能先于进行性纤维化间质性肺病 (ILD) 的蜂窝肺形成。SCGB1A1 支气管特异性克拉细胞可能在这一异常再生过程中发挥作用。评估患有 ILD 的患者的小气道中是否存在克拉细胞。对 14 名患有 ILD 和 10 名对照者的肺组织标本[外科肺活检 (SLB) 和/或经支气管肺冷冻活检 (TBLC)]的小气道进行形态学评估,并对 SCGB1A1 进行染色。SCGB1A1 作为气道生成的标志物(SCGB1A1/EH),按上皮高度加权。评估临床、功能和高分辨率 CT(HRCT)预后因素与组织形态计量学之间的相关性。ILD 模式样本的小气道中 SCGB1A1 细胞的密度明显较低[0.064(0.020-0.172)],而对照组样本的小气道中 SCGB1A1 细胞的密度较高[0.393(0.082-0.698)],<0.0001。常见间质性肺炎 (UIP) 模式最常包含 SCGB1A1 表达有限或缺失的小气道(SCGB1A1/EH <0.025):UIP(18/33;55%)与非 UIP 模式(4/31;13%)或对照组(0/29;0%)相比:<0.0001。此外,与 HRCT 的相关性表明,SCGB1A1 与支气管扩张呈显著负相关,支气管扩张是小气道化生的特征(Rho -0.63,<0.001),与用力肺活量 (FVC) 和峰度 HU 分布模式呈正相关(Rho 0.38 和 0.50,均<0.001),这是纤维化变化的标志物。与对照组相比,ILD 患者的小气道中更常缺乏 SCGB1A1,尤其是 UIP 患者。SCGB1A1 标记细胞的密度较低与支气管扩张和纤维化变化相关。进一步研究 SCGB1A1 染色作为小气道化生过程的病理特征是值得的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b12e/7952638/597e5b8ac067/fimmu-12-630096-g0001.jpg

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