Niessen Natalie M, Baines Katherine J, Simpson Jodie L, Scott Hayley A, Qin Ling, Gibson Peter G, Fricker Michael
Priority Research Centre for Healthy Lungs, The University of Newcastle, Newcastle, NSW, Australia.
National Health and Medical Research Council Centre of Excellence in Severe Asthma, Newcastle, NSW, Australia.
Clin Exp Allergy. 2021 Feb;51(2):305-317. doi: 10.1111/cea.13811. Epub 2021 Jan 1.
Monocytes and macrophages are critical innate immune cells of the airways. Despite their differing functions, few clinical studies discriminate between them and little is known about their regulation in asthma.
We aimed to distinguish and quantify macrophages, monocytes and monocyte subsets in induced sputum and blood and examine their relationship with inflammatory and clinical features of asthma.
We applied flow cytometry to distinguish macrophages, monocytes and subsets in sputum and blood (n = 53; 45 asthma, 8 non-asthma) and a second asthma sputum cohort (n = 26). Monocyte subsets were identified by surface CD14/CD16 (CD14 CD16 classical, CD14 CD16 intermediate and CD14 CD16 non-classical monocytes). Surface CD206, a marker of monocyte tissue differentiation, was measured in sputum. Relationship to airway inflammatory phenotype (neutrophilic n = 9, eosinophilic n = 14, paucigranulocytic n = 22) and asthma severity (severe n = 12, non-severe n = 33) was assessed.
Flow cytometry- and microscope-quantified sputum differential cell proportions were significantly correlated. Sputum macrophage number was reduced (p = .036), while classical monocyte proportion was increased in asthma vs non-asthma (p = .032). Sputum classical monocyte number was significantly higher in neutrophilic vs paucigranulocytic asthma (p = .013). CD206 monocyte proportion and number were increased in neutrophilic vs eosinophilic asthma (p < .001, p = .013). Increased sputum classical and CD206 monocyte numbers in neutrophilic asthma were confirmed in the second cohort. Blood monocytes did not vary with airway inflammatory phenotype, but blood classical monocyte proportion and number were increased in severe vs non-severe asthma (p = .022, p = .011).
Flow cytometry allowed distinction of sputum macrophages, monocytes and subsets, revealing compartment-specific dysregulation of monocytes in asthma. We observed an increase in classical and CD206 monocytes in sputum in neutrophilic asthma, suggesting co-recruitment of monocytes and neutrophils to the airways in asthma. Our data suggest further investigation of how airway monocyte dysregulation impacts on asthma-related disease activity is merited.
单核细胞和巨噬细胞是气道关键的固有免疫细胞。尽管它们功能不同,但很少有临床研究对二者进行区分,且对它们在哮喘中的调节机制知之甚少。
我们旨在区分并定量诱导痰和血液中的巨噬细胞、单核细胞及单核细胞亚群,并研究它们与哮喘炎症和临床特征的关系。
我们应用流式细胞术区分痰和血液中的巨噬细胞、单核细胞及其亚群(n = 53;45例哮喘患者,8例非哮喘患者),以及另一组哮喘痰样本队列(n = 26)。通过表面CD14/CD16鉴定单核细胞亚群(CD14⁺CD16⁻为经典单核细胞,CD14⁺CD16⁺为中间型单核细胞,CD14⁻CD16⁺为非经典单核细胞)。测量痰中表面CD206,这是单核细胞组织分化的标志物。评估其与气道炎症表型(嗜中性粒细胞性n = 9,嗜酸性粒细胞性n = 14,少粒细胞性n = 22)和哮喘严重程度(重度n = 12,非重度n = 33)的关系。
流式细胞术和显微镜定量的痰中不同细胞比例显著相关。与非哮喘相比,哮喘患者痰中巨噬细胞数量减少(p = 0.036),而经典单核细胞比例增加(p = 0.032)。嗜中性粒细胞性哮喘患者痰中经典单核细胞数量显著高于少粒细胞性哮喘患者(p = 0.013)。嗜中性粒细胞性哮喘与嗜酸性粒细胞性哮喘相比,痰中CD206单核细胞比例和数量增加(p < 0.001,p = 0.013)。在第二个队列中证实了嗜中性粒细胞性哮喘患者痰中经典单核细胞和CD206单核细胞数量增加。血液单核细胞与气道炎症表型无关,但重度哮喘与非重度哮喘相比,血液中经典单核细胞比例和数量增加(p = 0.022,p = 0.011)。
流式细胞术能够区分痰中的巨噬细胞、单核细胞及其亚群,揭示哮喘中单核细胞在不同部位的失调情况。我们观察到嗜中性粒细胞性哮喘患者痰中经典单核细胞和CD206单核细胞增加,提示哮喘中单核细胞和嗜中性粒细胞共同被募集到气道。我们的数据表明,值得进一步研究气道单核细胞失调如何影响哮喘相关疾病活动。