Division of Pediatric Allergy and Immunology, Mount Sinai School of Medicine, New York, New York 10029-6574, USA.
Ann Allergy Asthma Immunol. 2011 Mar;106(3):205-13. doi: 10.1016/j.anai.2010.11.019. Epub 2011 Jan 14.
Clinical outcomes of patients with asthma are highly variable. Immunological biomarkers associated with asthma control have not been elucidated.
To identify the association between clinical control of asthma and serum immunological profiles of asthmatics and compare these profiles with those of healthy controls by using a multiplex assay.
Sera were obtained from 28 nonsmokers 18 to 55 years of age with moderate and severe persistent asthma. Patients were classified as having well-controlled (WC, n = 14) or poorly controlled (PC, n = 14) asthma based on their responses to the Asthma Control Questionnaire and Asthma Quality of Life Questionnaire. Sera from nonasthmatic control individuals (NAC, n = 14) were used for comparison. Levels of 50 analytes, including cytokines, chemokines, angiogenic, and growth factors, were determined, using a multiplex assay.
Twelve of the 29 cytokines levels were significantly higher in patients with asthma than in NACs, but only interferon gamma levels were significantly lower in patients with asthma than in the NAC group. Among these, interleukin (IL)-3 and IL-18 levels were significantly higher in the PC group than the WC group. Five of the 12 tested chemokine levels were significantly higher in patients with asthma than in NACs. Five of six growth factor levels were significantly higher in patients with asthma than in NACs, and 3 were higher in PC than WC. Interleukin-18, fibroblast growth factor, hepatocyte growth factor, and stem cell growth factor-beta were positively correlated with poor asthma control and negatively with quality of life scores.
Increased serum levels of fibroblast growth factor, hepatocyte growth factor, and stem cell growth factor-beta might be useful biomarkers of asthma control status and targets of future asthma therapy.
哮喘患者的临床结局差异很大。与哮喘控制相关的免疫学标志物尚未阐明。
通过多重分析检测,确定哮喘患者临床控制与血清免疫学特征之间的关系,并将这些特征与健康对照者进行比较。
收集 28 名年龄在 18 至 55 岁之间、不吸烟的中重度持续性哮喘患者的血清。根据哮喘控制问卷和哮喘生活质量问卷的应答情况,将患者分为控制良好(WC)组(n = 14)和控制不佳(PC)组(n = 14)。使用非哮喘对照者(NAC)的血清进行比较。采用多重分析检测,测定 50 种分析物(包括细胞因子、趋化因子、血管生成和生长因子)的水平。
29 种细胞因子中有 12 种在哮喘患者中的水平明显高于 NAC 组,但只有干扰素γ水平在哮喘患者中明显低于 NAC 组。其中,IL-3 和 IL-18 水平在 PC 组中明显高于 WC 组。在 12 种检测到的趋化因子中,有 5 种在哮喘患者中的水平明显高于 NAC 组。5 种生长因子水平在哮喘患者中明显高于 NAC 组,3 种在 PC 组中高于 WC 组。IL-18、成纤维细胞生长因子、肝细胞生长因子和干细胞生长因子-β与哮喘控制不良呈正相关,与生活质量评分呈负相关。
成纤维细胞生长因子、肝细胞生长因子和干细胞生长因子-β的血清水平升高可能是哮喘控制状态的有用生物标志物,也是未来哮喘治疗的靶点。