Severe therapy resistant asthma in children: translational approaches to uncover sub-phenotypes
File(s)EXPERT_review-final-150617 revision-SS.docx (112.33 KB)
Accepted version
Author(s)
Alonso, AM
Fainardi, V
Saglani, S
Type
Journal Article
Abstract
Introduction: Paediatric severe therapy resistant asthma (STRA) affects a very small proportion of all children with asthma, but results in significant morbidity, has a high risk of mortality and utilises approximately half of all healthcare resources for childhood asthma. children with STRA need add-on ‘beyond guidelines’ therapies because of poor control despite maximal conventional treatments and optimisation of basic asthma management. however, STRA is heterogeneous with marked phenotypic variation between patients and mechanisms from adult severe asthma cannot be extrapolated to children.
Areas covered: This review will cover our current knowledge of paediatric STRA pathophysiology, with examples of translational approaches that have been used to define sub-phenotypes including; 1. pre-clinical age-appropriate models using clinically relevant allergens, 2. in vitro techniques incorporating complex co-cultures of structural and inflammatory cells, and 3. techniques that allow detailed cellular immunophenotyping of small airway samples will be discussed. Studies using these approaches that have demonstrated the importance of the innate mediator IL-33 and vitamin D deficiency in severe steroid resistant disease will also be discussed.
Expert commentary: These experimental approaches allow investigation of age and disease specific molecular pathways and the development of personalised therapies that can be stratified and targeted to sub-phenotypes of paediatric STRA.
Areas covered: This review will cover our current knowledge of paediatric STRA pathophysiology, with examples of translational approaches that have been used to define sub-phenotypes including; 1. pre-clinical age-appropriate models using clinically relevant allergens, 2. in vitro techniques incorporating complex co-cultures of structural and inflammatory cells, and 3. techniques that allow detailed cellular immunophenotyping of small airway samples will be discussed. Studies using these approaches that have demonstrated the importance of the innate mediator IL-33 and vitamin D deficiency in severe steroid resistant disease will also be discussed.
Expert commentary: These experimental approaches allow investigation of age and disease specific molecular pathways and the development of personalised therapies that can be stratified and targeted to sub-phenotypes of paediatric STRA.
Date Issued
2017-08-21
Date Acceptance
2017-08-14
Citation
Expert Review of Respiratory Medicine, 2017, 11 (11), pp.867-874
ISSN
1747-6348
Publisher
Taylor & Francis
Start Page
867
End Page
874
Journal / Book Title
Expert Review of Respiratory Medicine
Volume
11
Issue
11
Copyright Statement
© 2017 Informa UK Limited, trading as Taylor & Francis Group
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000414150700003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Respiratory System
Severe asthma
mechanisms
pathology
phenotypes
children
INNATE LYMPHOID-CELLS
SEVERE EOSINOPHILIC ASTHMA
PROBLEMATIC SEVERE ASTHMA
CORTICOSTEROID RESPONSE
AIRWAY INFLAMMATION
PEDIATRIC-PATIENTS
BLOOD EOSINOPHILS
DISEASE SEVERITY
CHILDHOOD
MICE
Publication Status
Published