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支气管肺泡灌洗液中的趋化因子受体CXCR3配体:与结节病的放射学表现、临床病程及预后的关联

Chemokine receptor CXCR3 ligands in bronchoalveolar lavage fluid: associations with radiological pattern, clinical course, and prognosis in sarcoidosis.

作者信息

Piotrowski Wojciech J, Młynarski Wojciech, Fendler Wojciech, Wyka Krystyna, Marczak Jerzy, Górski Paweł, Antczak Adam

出版信息

Pol Arch Med Wewn. 2014;124(7-8):395-402. doi: 10.20452/pamw.2349. Epub 2014 May 23.

Abstract

INTRODUCTION

Sustained inflammation in sarcoidosis may lead to lung fibrosis. The activity of numerous chemokines responsible for proliferation and activity of T lymphocytes may play a crucial role in this process and may have predictive value. These include cytokines induced by interferon γ, such as CXCL9, 10, and 11-ligands of chemokine receptor CXCR3.

OBJECTIVES

The aim of the study was to estimate the role of CXCR3 ligands in the pathogenesis of sarcoidosis and the predictive value of their concentrations in bronchoalveolar lavage (BAL) fluid.

PATIENTS AND METHODS

CXCL9, 10, and 11 concentrations in BAL fluid were measured by an enzyme‑linked immunosorbent assay in patients with sarcoidosis (n = 59) and controls (n = 34). A total of 46 patients were followed up for 24 months to compare the results between the subgroups with complete remission and with chronic disease.

RESULTS

Protein-standardized CXCL11 concentrations in BAL fluid from patients with stage II sarcoidosis were higher than in those with stage I (median [interquarile range], 0.95 [0.26-2.39] vs. 0.32 [0.13-0.74] pg/μg protein, P = 0.02). CXCL10 levels in BAL fluid from patients without Löfgren syndrome were higher compared with those the syndrome (0.69 [0.51-1.05] vs. 0.40 [0.27-0.70] pg/μg protein, P = 0.05). None of these markers predicted the chronic course of the disease. CXCL10 levels in BAL fluid correlated with serum angiotensin‑converting enzyme, and CXCL11 levels with parenchymal lesions on high‑resolution computed tomography. Only nonstandardized CXC11 concentrations in BAL fluid were higher in sarcoidosis.

CONCLUSIONS

Our results support the hypothesis that cytokines CXCL9, 10, and 11 may be involved in the pathogenesis of chronic sarcoidosis. However, the lack of notable differences between the sarcoidosis and control groups, as well as the lack of associations with the chronic course suggest that they should not be considered as potential prognostic markers.

摘要

引言

结节病中的持续性炎症可能导致肺纤维化。众多负责T淋巴细胞增殖和活性的趋化因子的活性可能在此过程中起关键作用,并且可能具有预测价值。这些趋化因子包括由干扰素γ诱导的细胞因子,如趋化因子受体CXCR3的配体CXCL9、10和11。

目的

本研究旨在评估CXCR3配体在结节病发病机制中的作用及其在支气管肺泡灌洗(BAL)液中浓度的预测价值。

患者与方法

采用酶联免疫吸附测定法测量结节病患者(n = 59)和对照组(n = 34)BAL液中CXCL9、10和11的浓度。共对46例患者进行了24个月的随访,以比较完全缓解亚组和慢性病亚组的结果。

结果

II期结节病患者BAL液中经蛋白质标准化的CXCL11浓度高于I期患者(中位数[四分位间距],0.95[0.26 - 2.39]对0.32[0.13 - 0.74] pg/μg蛋白质,P = 0.02)。无 Löfgren 综合征患者BAL液中的CXCL10水平高于有该综合征的患者(0.69[0.51 - 1.05]对0.40[0.27 - 0.70] pg/μg蛋白质,P = 0.05)。这些标志物均未预测疾病的慢性病程。BAL液中的CXCL10水平与血清血管紧张素转换酶相关,CXCL11水平与高分辨率计算机断层扫描上的实质病变相关。仅BAL液中未标准化的CXC11浓度在结节病中较高。

结论

我们的结果支持以下假设,即细胞因子CXCL9、10和11可能参与慢性结节病的发病机制。然而,结节病组与对照组之间缺乏显著差异,以及与慢性病程缺乏关联表明,它们不应被视为潜在的预后标志物。

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