Literature DB >> 28501346

IL-13 and idiopathic pulmonary fibrosis: Possible links and new therapeutic strategies.

Giovanni Passalacqua1, Marcello Mincarini2, Daniele Colombo2, Giuseppe Troisi2, Marta Ferrari2, Diego Bagnasco2, Francesco Balbi2, Annamaria Riccio2, Giorgio Walter Canonica2.   

Abstract

The recent advances in the knowledge of immunological aspects of many pulmonary diseases, allowed to identify cells, biological functions, cytokines, and receptors that are preferentially involved in each disease. This is the case of asthma, where IL-13 (together with IL-4) is recognized as a central mediator. The role of IL-13 is strictly related, via complex signaling pathways, to eosinophil recruitment and activation, to mucus secretion, periostin generation and to fibrogenic processes (which are part of the remodeling process). These peculiar roles of IL-13 have suggested the hypothesis of its role in Idiopathic Pulmonary Fibrosis, and consequently of its antagonists in the treatment of such disease. We review herein the immunological roles of IL-13 in asthma and IPF, and the currently ongoing attempts to treat IPF by IL-13 antagonism strategies.
Copyright © 2017. Published by Elsevier Ltd.

Entities:  

Keywords:  Asthma; Eosinophilic inflammation; Idiopathic pulmonary fibrosis; Interleukin 13; Periostin

Mesh:

Substances:

Year:  2017        PMID: 28501346     DOI: 10.1016/j.pupt.2017.05.007

Source DB:  PubMed          Journal:  Pulm Pharmacol Ther        ISSN: 1094-5539            Impact factor:   3.410


  18 in total

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