Department of Infection, Immunity and Cardiovascular Diseases, University of Sheffield, Sheffield, United Kingdom; Florey Institute, University of Sheffield, Sheffield, United Kingdom.
Division of Systems Medicine, University of Dundee, Ninewells Hospital and Medical School, Dundee, Scotland, United Kingdom.
Chest. 2022 May;161(5):1180-1191. doi: 10.1016/j.chest.2021.11.014. Epub 2021 Nov 25.
Nontuberculous mycobacterial (NTM) infections are difficult to diagnose and treat. Biomarkers to identify patients with active infection or at risk of disease progression would have clinical utility. Sputum is the most frequently used matrix for the diagnosis of NTM lung disease.
Can sputum proteomics be used to identify NTM-associated inflammatory profiles in sputum?
Patients with NTM lung disease and a matched cohort of patients with COPD, bronchiectasis (BE), and cystic fibrosis (CF) without NTM lung disease were enrolled from two hospitals in the United Kingdom. Liquid chromatography-tandem mass spectrometry was used to identify proteomic biomarkers associated with underlying diagnosis (COPD, BE, and CF), the presence of NTM lung disease defined according to American Thoracic Society/Infectious Diseases Society of America criteria, and severity of NTM. A subset of patients receiving guideline-concordant NTM treatment were studied to identify protein changes associated with treatment response.
This study analyzed 95 sputum samples from 55 subjects (BE, n = 21; COPD, n = 19; CF, n = 15). Underlying disease and infection with Pseudomonas aeruginosa were the strongest drivers of sputum protein profiles. Comparing protein abundance in COPD, BE, and CF found that 12 proteins were upregulated in CF compared with COPD, including MPO, AZU1, CTSG, CAT, and RNASE3, with 21 proteins downregulated, including SCGB1A1, IGFBP2, SFTPB, GC, and CFD. Across CF, BE, and COPD, NTM infection (n = 15) was not associated with statistically significant differences in sputum protein profiles compared with those without NTM. Two proteins associated with iron chelation were significantly downregulated in severe NTM disease. NTM treatment was associated with heterogeneous changes in the sputum protein profile. Patients with NTM and a decrease in immune response proteins had a subjective symptomatic improvement.
Sputum proteomics identified candidate biomarkers of NTM severity and treatment response. However, underlying lung disease and typical bacterial pathogens such as P aeruginosa are also key determinants of the sputum proteomic profile.
非结核分枝杆菌(NTM)感染难以诊断和治疗。能够识别活动性感染或疾病进展风险的生物标志物将具有临床应用价值。痰液是诊断 NTM 肺病最常用的基质。
痰液蛋白质组学能否用于识别痰液中与 NTM 相关的炎症特征?
从英国的两家医院招募了 NTM 肺病患者和匹配的 COPD、支气管扩张症(BE)和囊性纤维化(CF)患者队列,这些患者无 NTM 肺病。采用液相色谱-串联质谱法鉴定与潜在诊断(COPD、BE 和 CF)相关的蛋白质组学生物标志物,根据美国胸科学会/传染病学会标准定义 NTM 肺病的存在,以及 NTM 的严重程度。研究了接受指南一致的 NTM 治疗的患者亚组,以确定与治疗反应相关的蛋白质变化。
本研究分析了 55 名患者的 95 份痰样本(BE,n=21;COPD,n=19;CF,n=15)。基础疾病和铜绿假单胞菌感染是痰液蛋白谱的最强驱动因素。比较 COPD、BE 和 CF 中的蛋白质丰度发现,CF 中 12 种蛋白质与 COPD 相比上调,包括 MPO、AZU1、CTSG、CAT 和 RNASE3,21 种蛋白质下调,包括 SCGB1A1、IGFBP2、SFTPB、GC 和 CFD。在 CF、BE 和 COPD 中,与无 NTM 相比,NTM 感染(n=15)与痰液蛋白谱无统计学显著差异。与铁螯合相关的两种蛋白质在严重的 NTM 疾病中显著下调。NTM 治疗与痰液蛋白谱的异质变化相关。NTM 患者的免疫反应蛋白减少,其症状主观改善。
痰液蛋白质组学鉴定了 NTM 严重程度和治疗反应的候选生物标志物。然而,基础肺病和典型的细菌病原体如铜绿假单胞菌也是痰液蛋白质组谱的关键决定因素。