The prevalence, heterogeneity, and severity of type 2 inflammatory diseases, including asthma and atopic dermatitis, continue to rise, especially in children and adolescents. Type 2 inflammation is mediated by both innate and adaptive immune cells and sustained by a specific subset of cytokines, such as interleukin (IL)-4, IL-5,IL-13, and IgE. IL-4 and IL-13 are considered signature type 2 cytokines, as they both have a pivotal role in many of the pathobiologic changes featured in asthma and atopic dermatitis. Several biologics targeting IL-4, IL-5, and IL-13, as well as IgE, have been proposed to treat severe allergic disease in the pediatric population with promising results. A better definition of type 2 inflammatory pathways is essential to implement targeted therapeutic strategies.

Type-2 inflammatory mediators as targets for precision medicine in children

Manti S.;
2020-01-01

Abstract

The prevalence, heterogeneity, and severity of type 2 inflammatory diseases, including asthma and atopic dermatitis, continue to rise, especially in children and adolescents. Type 2 inflammation is mediated by both innate and adaptive immune cells and sustained by a specific subset of cytokines, such as interleukin (IL)-4, IL-5,IL-13, and IgE. IL-4 and IL-13 are considered signature type 2 cytokines, as they both have a pivotal role in many of the pathobiologic changes featured in asthma and atopic dermatitis. Several biologics targeting IL-4, IL-5, and IL-13, as well as IgE, have been proposed to treat severe allergic disease in the pediatric population with promising results. A better definition of type 2 inflammatory pathways is essential to implement targeted therapeutic strategies.
2020
Inglese
Si
Si, OA ibrido
Blackwell Publishing Ltd
31
26
17
19
3
https://www.authorea.com/users/340022/articles/467159-type-2-inflammatory-mediators-as-targets-for-precision-medicine-in-children
Internazionale
Esperti anonimi
asthma; atopic dermatitis; biologics; children; type 2 inflammation
no
info:eu-repo/semantics/article
Castagnoli, R.; Licari, A.; Manti, S.; Chiappini, E.; Marseglia, G. L.
14.a Contributo in Rivista::14.a.1 Articolo su rivista
5
262
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3239563
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