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About:
Airway Interleukin-33 and type 2 cytokines in adult patients with acute asthma
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schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Airway Interleukin-33 and type 2 cytokines in adult patients with acute asthma
Creator
Khoo, Siew-Kim
Laing, Ingrid
Backer, Vibeke
Baltic, Svetlana
Barrett, Lucy
Bjerregaard, Asger
Le Souëf, Peter
Porsbjerg, Celeste
Poulsen, Nadia
Cohen, Suzanne
Rapley, Laura
Thompson, Philip
Source
Elsevier; Medline; PMC
abstract
Abstract Background Several animal studies, and one inoculation study in adult asthmatics have shown that interleukin-33 (IL-33) is a major contributor to type-2 inflammation in acute asthma. However, the link between IL-33 and type-2 inflammation has not been shown in naturally occurring asthma exacerbations. Objectives To determine if airway IL-33 is associated with type-2 inflammation measured by type-2 cytokines, FeNO and sputum eosinophils in patients presenting to the Emergency Department with an asthma exacerbations. Methods Adult patients hospitalized due to acute asthma were enrolled. Upper airways were sampled with nasal swabs and lower airways with induced sputum. Cytokines were measured at protein level using a Luminex® assay and mRNA expression level using droplet-digital-PCR. Airway sampling was repeated four weeks after exacerbation. Results At the time of exacerbation, upper airway IL-33 correlated with upper airway IL-5 and IL-13 (R = 0.84, p < 0.01 and R = 0.76, p < 0.01, respectively) and with lower airway IL-13 (R = 0.49, p = 0.03). Similar associations were observed for mRNA expression. Lower airway IL-33 positively correlated with lower airway IL-13 (R = 0.84, p < 0.01). IL-13 and IL-33 were positively correlated with FeNO, and IL-5 with eosinophils. The association between IL-33 and type-2 cytokines were still present four weeks after exacerbation. Conclusion This is the first study to demonstrate that airway IL-33 is associated with type-2 cytokines in naturally occurring asthma exacerbations in adults, providing in vivo evidence supporting that IL-33 may be driving type-2 inflammation in acute asthma. Thus supporting IL-33 as a potential future drug target due to its role, upstream in the immunological cascade.
has issue date
2018-07-31
(
xsd:dateTime
)
bibo:doi
10.1016/j.rmed.2018.05.016
bibo:pmid
29957280
has license
els-covid
sha1sum (hex)
fe00f479396b82f2ab95abadb67f2c7881bb0776
schema:url
https://doi.org/10.1016/j.rmed.2018.05.016
resource representing a document's title
Airway Interleukin-33 and type 2 cytokines in adult patients with acute asthma
has PubMed Central identifier
PMC7172141
has PubMed identifier
29957280
schema:publication
Respiratory Medicine
resource representing a document's body
covid:fe00f479396b82f2ab95abadb67f2c7881bb0776#body_text
is
schema:about
of
named entity 'naturally'
named entity 'potential'
named entity 'Adult'
named entity 'This'
named entity 'adult'
named entity 'correlated'
named entity 'immunological'
named entity 'adult'
named entity 'asthma'
named entity 'IS A'
named entity 'LUMINEX'
named entity 'METHODS'
named entity 'CONTRIBUTOR'
named entity 'OBSERVED'
named entity 'INFLAMMATION'
named entity 'PATIENTS'
named entity 'Cytokines'
named entity 'measured'
named entity 'Methods'
named entity 'expression'
named entity 'study'
named entity 'eosinophils'
named entity 'IL-33'
named entity 'Conclusion'
named entity 'IL-33'
named entity 'cytokines'
named entity 'However'
named entity 'sputum'
named entity 'Airway'
named entity 'future'
named entity 'vivo'
named entity 'inoculation'
named entity 'IL-13'
named entity 'adults'
named entity 'upper airway'
named entity 'acute asthma'
named entity 'interleukin-33'
named entity 'Lower airway'
named entity 'FeNO'
named entity 'asthma exacerbations'
named entity 'IL-33'
named entity 'IL-33'
named entity 'IL-33'
named entity 'acute asthma'
named entity 'inflammation'
named entity 'inoculation'
named entity 'assay'
named entity 'lower airway'
named entity 'IL-13'
named entity 'immunological'
named entity 'PCR'
named entity 'inflammation'
named entity 'positively correlated'
named entity 'IL-13'
named entity 'Emergency Department'
named entity 'sputum'
named entity 'type 2'
named entity 'Interleukin-33'
named entity 'cytokines'
named entity 'Thus'
named entity 'IL-33'
named entity 'IL-5'
named entity 'acute asthma'
named entity 'log-transformation'
named entity 'inflammation'
named entity 'FeNO'
named entity 'asthma'
named entity 'HKU1'
named entity 'inflammation'
named entity 'mRNA expression'
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