Fraunhofer Institute of Toxicology and Experimental Medicine, Hannover, Germany.
Fraunhofer Institute of Toxicology and Experimental Medicine, Hannover, Germany.
Ann Allergy Asthma Immunol. 2017 Mar;118(3):290-297. doi: 10.1016/j.anai.2017.01.018.
Allergic rhinitis is an inflammatory disease that causes cellular influx and mediator release in the nose. These inflammatory changes might be used as nasal biomarkers to assess the efficacy of novel anti-allergic treatments.
To assess the specificity and reproducibility of nasal biomarkers in patients with allergic rhinitis after grass pollen exposure in an allergen challenge chamber.
In a monocenter pilot study, 15 patients with allergic rhinitis and 19 healthy individuals underwent two 4-hour Dactylis glomerate pollen challenges in the challenge chamber with an interval of 21 days. Before challenge, on exit, and after 2 and 22 hours, a nasal lavage was performed and nasal secretions were collected on filter paper to determine a wide panel of cells and mediators. Furthermore, total nasal symptom score, nasal flow, and nasal nitric oxide were measured.
Pollen exposure significantly increased eosinophil, interleukin (IL) 5, IL-6, IL-13, and macrophage inflammatory protein 1β levels in allergic patients but not in healthy individuals. The effect could be reproduced for eosinophils, IL-5, IL-6, and macrophage inflammatory protein 1β after the second allergen challenge. By contrast, the IL-13 levels were higher and eotaxin levels first increased after repetitive allergen challenge. There was no correlation between total nasal symptom score and elevated cell or cytokine levels. Nasal nitric oxide levels were nonspecifically elevated in both patients with allergy and healthy controls.
A subset of cellular and soluble biomarkers in nasal lavage and secretion reveals specificity and reproducibility in patients with allergic rhinitis. These can be used to measure the immunologic efficacy of antiallergic treatments in an allergen challenge chamber. Carryover effects attributable to priming must be considered when designing cross-over studies.
clinicaltrials.gov Identifier: NCT00297843.
变应性鼻炎是一种炎症性疾病,可导致鼻内细胞浸润和介质释放。这些炎症变化可作为鼻生物标志物,用于评估新型抗过敏治疗的疗效。
评估变应性鼻炎患者在变应原激发室内进行草花粉暴露后,鼻生物标志物的特异性和可重复性。
在一项单中心的初步研究中,15 例变应性鼻炎患者和 19 例健康个体在变应原激发室内接受了两次为期 4 小时的梯牧草花粉激发,两次激发间隔 21 天。在激发前、激发后及 2 小时和 22 小时时,进行鼻冲洗,并在滤纸上收集鼻分泌物,以确定广泛的细胞和介质。此外,还测量了总鼻症状评分、鼻流量和鼻内一氧化氮。
花粉暴露显著增加了变应性鼻炎患者的嗜酸性粒细胞、白细胞介素(IL)-5、IL-6、IL-13 和巨噬细胞炎性蛋白 1β水平,但在健康个体中没有增加。在第二次变应原激发后,可重复观察到嗜酸性粒细胞、IL-5、IL-6 和巨噬细胞炎性蛋白 1β的作用。相比之下,IL-13 水平在重复变应原激发后升高,而嗜酸性粒细胞趋化因子水平首先升高。总鼻症状评分与升高的细胞或细胞因子水平之间没有相关性。鼻内一氧化氮水平在变应性鼻炎患者和健康对照者中均非特异性升高。
鼻冲洗和分泌物中细胞和可溶性生物标志物的亚群在变应性鼻炎患者中具有特异性和可重复性。这些可用于在变应原激发室内测量抗过敏治疗的免疫疗效。在设计交叉研究时,必须考虑到由于引发作用而产生的残留效应。
clinicaltrials.gov 标识符:NCT00297843。