The central role of IL-33/IL-1RL1 pathway in asthma: From pathogenesis to intervention

A K Saikumar Jayalatha, L Hesse, M E Ketelaar, G H Koppelman, M C Nawijn*

*Bijbehorende auteur voor dit werk

Onderzoeksoutput: Review articlepeer review

2 Citaten (Scopus)
10 Downloads (Pure)


Interleukin-33 (IL-33), a member of the IL-1 family, and its cognate receptor, Interleukin-1 receptor like-1 (IL-1RL1 or ST2), are susceptibility genes for childhood asthma. In response to cellular damage, IL-33 is released from barrier tissues as an 'alarmin' to activate the innate immune response. IL-33 drives type 2 responses by inducing signalling through its receptor IL-1RL1 in several immune and structural cells, thereby leading to type 2 cytokine and chemokine production. IL-1RL1 gene transcript encodes different isoforms generated through alternative splicing. Its soluble isoform, IL-1RL1-a or sST2, acts as a decoy receptor by sequestering IL-33, thereby inhibiting IL1RL1-b/IL-33 signalling. IL-33 and its receptor IL-1RL1 are therefore considered as putative biomarkers or targets for pharmacological intervention in asthma. This review will provide an overview of the genetics and biology of the IL-33/IL-1RL1 pathway in the context of asthma pathogenesis. It will discuss the potential and complexities of targeting the cytokine or its receptor, how genetics or biomarkers may inform precision medicine for asthma targeting this pathway, and the possible positioning of therapeutics targeting IL-33 or its receptor in the expanding landscape of novel biologicals applied in asthma management.

Originele taal-2English
Aantal pagina's18
TijdschriftPharmacology & Therapeutics
Vroegere onlinedatum2-apr-2021
StatusE-pub ahead of print - 2-apr-2021

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