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本文引用的文献

1
The interleukin-33 receptor ST2 is important for the development of peripheral airway hyperresponsiveness and inflammation in a house dust mite mouse model of asthma.白细胞介素-33受体ST2在哮喘的屋尘螨小鼠模型中,对于外周气道高反应性和炎症的发展至关重要。
Clin Exp Allergy. 2016 Mar;46(3):479-90. doi: 10.1111/cea.12683.
2
Lebrikizumab in moderate-to-severe asthma: pooled data from two randomised placebo-controlled studies.瑞莎珠单抗治疗中重度哮喘:两项随机安慰剂对照研究的汇总数据
Thorax. 2015 Aug;70(8):748-56. doi: 10.1136/thoraxjnl-2014-206719. Epub 2015 May 22.
3
IL-33-dependent type 2 inflammation during rhinovirus-induced asthma exacerbations in vivo.鼻病毒诱导的体内哮喘加重过程中依赖白细胞介素-33的2型炎症反应
Am J Respir Crit Care Med. 2014 Dec 15;190(12):1373-82. doi: 10.1164/rccm.201406-1039OC.
4
Mepolizumab treatment in patients with severe eosinophilic asthma.美泊利珠单抗治疗严重嗜酸性粒细胞性哮喘患者。
N Engl J Med. 2014 Sep 25;371(13):1198-207. doi: 10.1056/NEJMoa1403290. Epub 2014 Sep 8.
5
Symptom- and fraction of exhaled nitric oxide-driven strategies for asthma control: A cluster-randomized trial in primary care.症状和呼出一氧化氮分数驱动的哮喘控制策略:初级保健中的一项集群随机试验。
J Allergy Clin Immunol. 2015 Mar;135(3):682-8.e11. doi: 10.1016/j.jaci.2014.07.016. Epub 2014 Aug 28.
6
IL-33 and thymic stromal lymphopoietin mediate immune pathology in response to chronic airborne allergen exposure.IL-33 和胸腺基质淋巴细胞生成素介导对慢性空气传播过敏原暴露的免疫病理学反应。
J Immunol. 2014 Aug 15;193(4):1549-59. doi: 10.4049/jimmunol.1302984. Epub 2014 Jul 11.
7
Improved molecular typing assay for rhinovirus species A, B, and C.针对A、B和C型鼻病毒的改进分子分型检测方法
J Clin Microbiol. 2014 Jul;52(7):2461-71. doi: 10.1128/JCM.00075-14. Epub 2014 Apr 30.
8
Anti-inflammatory treatment of atopic asthma guided by exhaled nitric oxide: a randomized, controlled trial.呼出气一氧化氮指导下的特应性哮喘抗炎治疗:一项随机对照试验。
J Allergy Clin Immunol Pract. 2013 Nov-Dec;1(6):639-48.e1-8. doi: 10.1016/j.jaip.2013.07.013. Epub 2013 Oct 9.
9
Frequent exacerbators--a distinct phenotype of severe asthma.频繁加重者——严重哮喘的一种特殊表型。
Clin Exp Allergy. 2014 Feb;44(2):212-21. doi: 10.1111/cea.12179.
10
Outcomes after cessation of mepolizumab therapy in severe eosinophilic asthma: a 12-month follow-up analysis.重度嗜酸性粒细胞性哮喘患者停用美泊利珠单抗治疗后的结局:一项12个月的随访分析。
J Allergy Clin Immunol. 2014 Mar;133(3):921-3. doi: 10.1016/j.jaci.2013.11.026. Epub 2014 Jan 10.

呼出气一氧化氮分数和痰液嗜酸性粒细胞升高与未来病毒诱发加重的风险增加相关:一项前瞻性队列研究。

High fractional exhaled nitric oxide and sputum eosinophils are associated with an increased risk of future virus-induced exacerbations: A prospective cohort study.

作者信息

Bjerregaard A, Laing I A, Backer V, Sverrild A, Khoo S-K, Chidlow G, Sikazwe C, Smith D W, Le Souëf P, Porsbjerg C

机构信息

Respiratory Research Unit, Bispebjerg University Hospital, Copenhagen, Denmark.

Telethon Kids Institute, Perth, WA, Australia.

出版信息

Clin Exp Allergy. 2017 Aug;47(8):1007-1013. doi: 10.1111/cea.12935. Epub 2017 May 9.

DOI:10.1111/cea.12935
PMID:28390083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7162064/
Abstract

BACKGROUND

The major trigger of asthma exacerbations is infection with a respiratory virus, most commonly rhinovirus. Type 2 inflammation is known to be associated with an increased risk of exacerbations in general. Whether type 2 inflammation at baseline increases the risk of future virus-induced exacerbations is unknown.

OBJECTIVE

To assess whether type 2 inflammation is associated with an increased risk of virus-induced exacerbations of asthma.

METHODS

Stable asthmatics had spirometry, skin prick test, measurement of FeNO and sputum induced for differential cell counts. Patients were followed up for 18 months, during which they were assessed at the research unit when they had symptoms of an exacerbation. Nasal swabs collected at these assessments underwent viral detection by PCR.

RESULTS

A total of 81 asthma patients were recruited, of which 22 (27%) experienced an exacerbation during the follow-up period. Of these, 15 (68%) had a respiratory virus detected at exacerbation. Sputum eosinophils >1% at baseline increased the risk of having a subsequent virus-induced exacerbation (HR 7.6 95% CI: 1.6-35.2, P=.010) as did having FeNO >25 ppb (HR 3.4 95% CI: 1.1-10.4, P=.033).

CONCLUSION AND CLINICAL RELEVANCE

Established type 2 inflammation during stable disease is a risk factor for virus-induced exacerbations in a real-life setting. Measures of type 2 inflammation, such as sputum eosinophils and FeNO, could be included in the risk assessment of patients with asthma in future studies.

摘要

背景

哮喘急性加重的主要诱因是呼吸道病毒感染,最常见的是鼻病毒。一般而言,已知2型炎症与急性加重风险增加有关。基线时的2型炎症是否会增加未来病毒诱发急性加重的风险尚不清楚。

目的

评估2型炎症是否与病毒诱发的哮喘急性加重风险增加有关。

方法

病情稳定的哮喘患者进行肺活量测定、皮肤点刺试验、呼出气一氧化氮(FeNO)测定以及诱导痰进行细胞分类计数。对患者进行18个月的随访,在此期间,当他们出现急性加重症状时在研究单位进行评估。在这些评估时采集的鼻拭子通过聚合酶链反应(PCR)进行病毒检测。

结果

共招募了81例哮喘患者,其中22例(27%)在随访期间出现急性加重。其中,15例(68%)在急性加重时检测到呼吸道病毒。基线时痰嗜酸性粒细胞>1%会增加随后病毒诱发急性加重的风险(风险比[HR] 7.6,95%置信区间[CI]:1.6 - 35.2,P = 0.010),FeNO>25 ppb时也是如此(HR 3.4,95% CI:1.1 - 10.4,P = 0.033)。

结论及临床意义

在稳定期疾病中已确立的2型炎症是现实生活中病毒诱发急性加重的危险因素。在未来研究中,2型炎症指标,如痰嗜酸性粒细胞和FeNO,可纳入哮喘患者的风险评估。