Karakioulaki Meropi, Berkemeier Caroline Maria, Grize Leticia, Heijnen Ingmar, Polyzos Stergios A, Goulas Antonis, Tamm Michael, Stolz Daiana
Clinic of Respiratory Medicine and Pulmonary Cell Research, University Hospital Basel, Switzerland; Clinic of Dermatology and Venereology, Medical Center-University of Freiburg, Germany; Faculty of Medicine, University of Freiburg, Germany.
Medical Immunology, Laboratory Medicine, University Hospital Basel, Basel, Switzerland.
Eur J Intern Med. 2025 Jun;136:71-81. doi: 10.1016/j.ejim.2025.04.001. Epub 2025 Apr 12.
Total Immunoglobulin E (tIgE) and allergen-specific IgE (sIgE) have been linked to asthma in numerous studies, with emerging evidence suggesting IgE sensitization influences chronic obstructive pulmonary disease (COPD) onset and severity. This study explores whether (a) serum tIgE and sIgE profiles differ among COPD, asthma, and controls (case-control substudy) and (b) tIgE and 300 individual sIgE levels correlate with disease severity and outcomes in 343 COPD patients (longitudinal substudy).
The case-control substudy measured tIgE and sIgE in 122 participants (76 COPD, 19 asthma, 27 controls). The longitudinal substudy analyzed tIgE and 300 sIgE in 343 COPD patients, examining links to disease severity and outcomes. Atopy was defined as tIgE>20 kUA/L, while skin-sensitization was determined by skin prick test positivity.
No significant tIgE differences were observed among asthma, COPD, and controls, however asthma and COPD patients showed distinct sIgE patterns for various allergens. Atopic men reported fewer urgent visits for acute exacerbations of COPD (ECOPD) than non-atopic men (79.07 % vs.91.33 %, p = 0.007), while skin-sensitized women experienced more severe ECOPD than non-skin-sensitized women (46.43 % vs. 24.36 %, p = 0.028). Exacerbation etiology was not associated with atopic or skin-sensitization profiles. Fungal sensitization correlated with older age (p = 0.032), worse 6-minute walking test outcomes (p = 0.007), and reduced diffusion capacity (DLCO/VA %, p = 0.006).
While atopic profiles are similar across groups, asthma features higher aeroallergen sIgE. Skin-sensitization and atopy may influence lung function and symptom severity in COPD but are differently associated with ECOPD between sexes and are not linked to the etiology of ECOPD.
在众多研究中,总免疫球蛋白E(tIgE)和变应原特异性IgE(sIgE)与哮喘相关,新出现的证据表明IgE致敏会影响慢性阻塞性肺疾病(COPD)的发病和严重程度。本研究探讨:(a)COPD、哮喘和对照组之间血清tIgE和sIgE谱是否存在差异(病例对照子研究);(b)343例COPD患者的tIgE和300种个体sIgE水平与疾病严重程度和预后是否相关(纵向子研究)。
病例对照子研究检测了122名参与者(76例COPD患者、19例哮喘患者、27名对照者)的tIgE和sIgE。纵向子研究分析了343例COPD患者的tIgE和300种sIgE,研究其与疾病严重程度和预后的关联。特应性定义为tIgE>20 kUA/L,皮肤致敏通过皮肤点刺试验阳性确定。
哮喘、COPD和对照组之间未观察到显著的tIgE差异,然而哮喘和COPD患者对各种变应原表现出不同的sIgE模式。特应性男性因COPD急性加重(ECOPD)的急诊就诊次数少于非特应性男性(79.07%对91.33%,p = 0.007),而皮肤致敏女性的ECOPD比非皮肤致敏女性更严重(46.43%对24.36%,p = 0.028)。加重病因与特应性或皮肤致敏谱无关。真菌致敏与年龄较大相关(p = 0.032)、6分钟步行试验结果较差(p = 0.007)以及弥散能力降低(DLCO/VA%,p = 0.006)。
虽然各组的特应性谱相似,但哮喘患者的气传变应原sIgE更高。皮肤致敏和特应性可能影响COPD患者的肺功能和症状严重程度,但在性别之间与ECOPD的关联不同,且与ECOPD的病因无关。