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慢性阻塞性肺疾病临床稳定期和加重期的炎症表型相关气道微生物组:一项多队列纵向分析。

Inflammatory Endotype-associated Airway Microbiome in Chronic Obstructive Pulmonary Disease Clinical Stability and Exacerbations: A Multicohort Longitudinal Analysis.

机构信息

Institute of Ecological Sciences, School of Life Sciences, South China Normal University, Guangzhou, China.

Medical Innovation, Value Evidence and Outcomes, and.

出版信息

Am J Respir Crit Care Med. 2021 Jun 15;203(12):1488-1502. doi: 10.1164/rccm.202009-3448OC.

Abstract

Understanding the role of the airway microbiome in chronic obstructive pulmonary disease (COPD) inflammatory endotypes may help to develop microbiome-based diagnostic and therapeutic approaches. To understand the association of the airway microbiome with neutrophilic and eosinophilic COPD at stability and during exacerbations. An integrative analysis was performed on 1,706 sputum samples collected longitudinally from 510 patients with COPD recruited at four UK sites of the BEAT-COPD (Biomarkers to Target Antibiotic and Systemic COPD), COPDMAP (Chronic Obstructive Pulmonary Disease Medical Research Council/Association of the British Pharmaceutical Industry), and AERIS (Acute Exacerbation and Respiratory Infections in COPD) cohorts. The microbiome was analyzed using COPDMAP and AERIS as a discovery data set and BEAT-COPD as a validation data set. The airway microbiome in neutrophilic COPD was heterogeneous, with two primary community types differentiated by the predominance of . The -predominant subgroup had elevated sputum IL-1β and TNFα (tumor necrosis factor α) and was relatively stable over time. The other neutrophilic subgroup with a balanced microbiome profile had elevated sputum and serum IL-17A and was temporally dynamic. Patients in this state at stability were susceptible to the greatest microbiome shifts during exacerbations. This subgroup can temporally switch to both neutrophilic and eosinophilic states that were otherwise mutually exclusive. Time-series analysis on the microbiome showed that the temporal trajectories of and were indicative of intrapatient switches from neutrophilic to eosinophilic inflammation, in track with patient sputum eosinophilia over time. Network analysis revealed distinct host-microbiome interaction patterns among neutrophilic -predominant, neutrophilic balanced microbiome, and eosinophilic subgroups. The airway microbiome can stratify neutrophilic COPD into subgroups that justify different therapies. Neutrophilic and eosinophilic COPD are interchangeable in some patients. Monitoring temporal variability of the airway microbiome may track patient inflammatory status over time.

摘要

了解气道微生物组在慢性阻塞性肺疾病(COPD)炎症表型中的作用,可能有助于开发基于微生物组的诊断和治疗方法。 研究气道微生物组与稳定期和加重期中性粒细胞性和嗜酸性粒细胞性 COPD 的关联。对来自英国四个地点的 BEAT-COPD(生物标志物靶向抗生素和系统性 COPD)、COPDMAP(慢性阻塞性肺疾病医学研究委员会/英国制药工业协会)和 AERIS(COPD 中的急性加重和呼吸道感染)队列的 510 名 COPD 患者的 1706 份纵向痰液样本进行了综合分析。使用 COPDMAP 和 AERIS 作为发现数据集,BEAT-COPD 作为验证数据集分析微生物组。 在中性粒细胞性 COPD 中,气道微生物组是异质的,有两种主要的群落类型,其特征是. 优势亚组痰液中 IL-1β 和 TNFα(肿瘤坏死因子α)升高,且随时间相对稳定。另一个具有平衡微生物组特征的中性粒细胞亚组,其痰液和血清中 IL-17A 升高,且随时间动态变化。在稳定期处于这种状态的患者在加重期更容易发生最大的微生物组变化。该亚组可暂时转变为中性粒细胞和嗜酸性粒细胞状态,这两种状态以前是相互排斥的。对微生物组的时间序列分析表明,和的时间轨迹表明患者体内从中性粒细胞炎症向嗜酸性粒细胞炎症的转变,与患者随时间推移的痰嗜酸性粒细胞增多相吻合。网络分析显示,在中性粒细胞占优势、中性粒细胞平衡微生物组和嗜酸性粒细胞亚组中,宿主-微生物组的相互作用模式存在明显差异。 气道微生物组可以将中性粒细胞性 COPD 分层为不同治疗的亚组。在一些患者中,中性粒细胞性和嗜酸性粒细胞性 COPD 是可以相互转化的。监测气道微生物组的时间变异性可能会随时间跟踪患者的炎症状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2418/8483235/4cc314df7837/rccm.202009-3448OCf1.jpg

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