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Immunological profiling in chronic rhinosinusitis with nasal polyps reveals distinct VEGF and GM-CSF signatures during symptomatic exacerbations.伴有鼻息肉的慢性鼻-鼻窦炎的免疫谱分析揭示了症状加重期间不同的血管内皮生长因子(VEGF)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)特征。
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本文引用的文献

1
Chronic rhinosinusitis, race, and ethnicity.慢性鼻-鼻窦炎,种族和民族。
Am J Rhinol Allergy. 2012 Mar-Apr;26(2):110-6. doi: 10.2500/ajra.2012.26.3741.
2
Pathophysiology of chronic rhinosinusitis with nasal polyp.慢性鼻-鼻窦炎伴鼻息肉的病理生理学。
Am J Rhinol Allergy. 2011 Sep-Oct;25(5):285-90. doi: 10.2500/ajra.2011.25.3680.
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Genetics and phenotyping in chronic sinusitis.慢性鼻窦炎的遗传学和表型分析。
J Allergy Clin Immunol. 2011 Oct;128(4):710-20; quiz 721-2. doi: 10.1016/j.jaci.2011.05.022. Epub 2011 Jun 25.
4
Acute exacerbations of chronic rhinosinusitis occur in a distinct seasonal pattern.慢性鼻窦炎的急性加重呈明显的季节性模式。
J Allergy Clin Immunol. 2010 Jul;126(1):168-9. doi: 10.1016/j.jaci.2010.03.041.
5
Evidence for altered activity of the IL-6 pathway in chronic rhinosinusitis with nasal polyps.慢性鼻息肉鼻窦炎患者白细胞介素 6 通路活性改变的证据。
J Allergy Clin Immunol. 2010 Feb;125(2):397-403.e10. doi: 10.1016/j.jaci.2009.10.072.
6
Contemporary assessment of the disease burden of sinusitis.鼻窦炎疾病负担的当代评估。
Am J Rhinol Allergy. 2009 Jul-Aug;23(4):392-5. doi: 10.2500/ajra.2009.23.3355.
7
Infection rate and virus-induced cytokine secretion in experimental rhinovirus infection in mucosal organ culture: comparison between specimens from patients with chronic rhinosinusitis with nasal polyps and those from normal subjects.鼻黏膜器官培养中实验性鼻病毒感染的感染率及病毒诱导的细胞因子分泌:鼻息肉型慢性鼻-鼻窦炎患者与正常受试者标本的比较
Arch Otolaryngol Head Neck Surg. 2008 Apr;134(4):424-7. doi: 10.1001/archotol.134.4.424.
8
Detection of rhinovirus in turbinate epithelial cells of chronic sinusitis.慢性鼻窦炎鼻甲骨上皮细胞中鼻病毒的检测
Am J Rhinol. 2006 Nov-Dec;20(6):634-6. doi: 10.2500/ajr.2006.20.2899.
9
Persistent inflammation and hyperresponsiveness following viral rhinosinusitis.病毒性鼻-鼻窦炎后的持续性炎症和高反应性。
Laryngoscope. 2006 Jul;116(7):1236-40. doi: 10.1097/01.mlg.0000224526.43698.52.
10
Rhinosinusitis: establishing definitions for clinical research and patient care.鼻窦炎:为临床研究和患者护理确立定义。
J Allergy Clin Immunol. 2004 Dec;114(6 Suppl):155-212. doi: 10.1016/j.jaci.2004.09.029.

一项用于研究慢性鼻-鼻窦炎加重期免疫变化的模型:一项初步研究的数据。

A proposed model to study immunologic changes during chronic rhinosinusitis exacerbations: data from a pilot study.

机构信息

Division of Allergy, Asthma, and Immunology, Mayo Clinic, Scottsdale, Arizona, USA.

出版信息

Am J Rhinol Allergy. 2013 Mar-Apr;27(2):98-101. doi: 10.2500/ajra.2013.27.3850.

DOI:10.2500/ajra.2013.27.3850
PMID:23562196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3610944/
Abstract

BACKGROUND

One way to gain insight into the pathophysiology of chronic rhinosinusitis (CRS) is to study the immunologic changes that occur with exacerbation. This study describes the immunologic changes during CRS exacerbation

METHODS

We performed a prospective study to investigate the immunologic changes seen during exacerbation of CRS with nasal polyposis. We recruited adult subjects who met clinical criteria for CRS with sinus CT scan within the past 5 years with Lund-Mackay score of >5 and nasal polyps. Subjects underwent a baseline visit with collection of nasal secretion and nasal wash. With acute worsening of symptoms, subjects underwent 6 near-consecutive-day collections and one follow-up collection 2 weeks later. IL-6, IL-33, eosinophil major basic protein (MBP), eosinophil-derived neurotoxin (EDN), myeloperoxidase (MPO), and uric acid were measured on the nasal samples from each visit.

RESULTS

A total of 10 subjects were recruited and 9 had acute worsening of CRS during the study period. Eight of the nine subjects were women and ages ranged from 26 to 56 years. At baseline, most inflammatory parameters were low and eight of the nine subjects were on intranasal corticosteroids. Compared with baseline measurements, IL-6, MBP, MPO, EDN, and uric acid were significantly elevated during CRS exacerbation. Levels of IL-6 and MBP (r = 0.47) levels as well as IL-6 and MPO (r = 0.75) were both significantly correlated (p < 0.01).

CONCLUSION

Prospective study of CRS exacerbations is feasible and provides insights into the immunologic mechanisms of CRS.

摘要

背景

了解慢性鼻-鼻窦炎(CRS)病理生理学的一种方法是研究加重时发生的免疫变化。本研究描述了 CRS 加重期间的免疫变化。

方法

我们进行了一项前瞻性研究,以研究伴有鼻息肉的 CRS 加重期间发生的免疫变化。我们招募了符合 CRS 临床标准的成年受试者,这些受试者在过去 5 年内进行了鼻窦 CT 扫描,Lund-Mackay 评分>5 分,且有鼻息肉。受试者进行基线就诊,采集鼻分泌物和鼻腔冲洗液。在症状急性恶化时,受试者连续 6 天进行采集,2 周后进行一次随访采集。在每次就诊时测量鼻样本中的白细胞介素-6(IL-6)、白细胞介素-33(IL-33)、嗜酸性粒细胞主要碱性蛋白(MBP)、嗜酸性粒细胞衍生神经毒素(EDN)、髓过氧化物酶(MPO)和尿酸。

结果

共招募了 10 名受试者,其中 9 名在研究期间出现 CRS 急性加重。9 名受试者中有 8 名是女性,年龄在 26 至 56 岁之间。在基线时,大多数炎症参数较低,9 名受试者中有 8 名正在使用鼻内皮质类固醇。与基线测量值相比,CRS 加重期间 IL-6、MBP、MPO、EDN 和尿酸均显著升高。IL-6 和 MBP 水平(r = 0.47)以及 IL-6 和 MPO 水平(r = 0.75)均呈显著相关性(p < 0.01)。

结论

CRS 加重的前瞻性研究是可行的,并提供了对 CRS 免疫机制的深入了解。