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Abundance of Non-Polarized Lung Macrophages with Poor Phagocytic Function in Chronic Obstructive Pulmonary Disease (COPD)

机译:丰富的非偏振肺巨噬细胞吞噬肺纤维疾病患者在慢性阻塞性肺疾病(COPD)中

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摘要

Lung macrophages are the key immune effector cells in the pathogenesis of Chronic Obstructive Pulmonary Disease (COPD). Several studies have shown an increase in their numbers in bronchoalveolar lavage fluid (BAL) of subjects with COPD compared to controls, suggesting a pathogenic role in disease initiation and progression. Although reduced lung macrophage phagocytic ability has been previously shown in COPD, the relationship between lung macrophages’ phenotypic characteristics and functional properties in COPD is still unclear. (1) Methods: Macrophages harvested from bronchoalveolar lavage (BAL) fluid of subjects with and without COPD (GOLD grades, I–III) were immuno-phenotyped, and their function and gene expression profiles were assessed using targeted assays. (2) Results: BAL macrophages from 18 COPD and 10 (non-COPD) control subjects were evaluated. The majority of macrophages from COPD subjects were non-polarized (negative for both M1 and M2 markers; 77.9%) in contrast to controls (23.9%; p < 0.001). The percentages of these non-polarized macrophages strongly correlated with the severity of COPD (p = 0.006) and current smoking status (p = 0.008). Non-polarized macrophages demonstrated poor phagocytic function in both the control (p = 0.02) and COPD (p < 0.001) subjects. Non-polarized macrophages demonstrated impaired ability to phagocytose Staphylococcus aureus (p < 0.001). They also demonstrated reduced gene expression for CD163, CD40, CCL13 and C1QA&B, which are involved in pathogen recognition and processing and showed an increased gene expression for CXCR4, RAF1, amphiregulin and MAP3K5, which are all involved in promoting the inflammatory response. (3) Conclusions: COPD is associated with an abundance of non-polarized airway macrophages that is related to the severity of COPD. These non-polarized macrophages are predominantly responsible for the poor phagocytic capacity of lung macrophages in COPD, having reduced capacity for pathogen recognition and processing. This could be a key risk factor for COPD exacerbation and could contribute to disease progression.
机译:肺巨噬细胞是慢性阻塞性肺病发病机制中的关键免疫效应细胞(COPD)。与对照组相比,几项研究表明,与COPD的受试者的支气管肺泡灌洗液(BAL)中的数量增加,表明疾病引发和进展中的致病作用。虽然降低了肺巨噬细胞吞噬能力,​​但先前已经在COPD中表现出,但肺巨噬细胞的表型特征与COPD中功能性能之间的关系仍然尚不清楚。 (1)方法:从带有和不带COPD(金等级,I-III)的受试者的支气管肺泡灌洗(BAL)流体收获的巨噬细胞是免疫表型的,并且使用靶向测定评估它们的功能和基因表达谱。 (2)结果:评估来自18个COPD和10个(非COPD)对照受试者的Bal巨噬细胞。来自COPD受试者的大多数巨噬细胞是非偏振的(对于M1和M2标记的阴性; 77.9%)与对照相比(23.9%; P <0.001)。这些非极化巨噬细胞的百分比与COPD的严重程度强烈相关(p = 0.006)和当前吸烟状态(p = 0.008)。非极化巨噬细胞在对照(P = 0.02)和COPD(P <0.001)受试者中表现出较差的吞噬功能。非偏振巨噬细胞证明了吞噬细胞金黄色葡萄球菌的能力(P <0.001)。它们还证明了CD163,CD40,CCL13和C1QA&B的基因表达,其参与病原体识别和加工,并显示CXCR4,RAF1,Amphiregulin和MAP3K5的增加,这些基因表达全部涉及促进炎症反应。 (3)结论:COPD与与COPD的严重程度有关的非极化气道巨噬细胞有关。这些非偏振巨噬细胞主要负责COPD中肺巨噬细胞的吞噬能力差,具有降低的病原体识别和加工能力。这可能是COPD加剧的关键危险因素,可以有助于疾病进展。

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