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  4. Type 2 chronic inflammatory diseases: targets, therapies and unmet needs
 
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2023
Review
Title

Type 2 chronic inflammatory diseases: targets, therapies and unmet needs

Abstract
Over the past two decades, significant progress in understanding of the pathogenesis of type 2 chronic inflammatory diseases has enabled the identification of compounds for more than 20 novel targets, which are approved or at various stages of development, finally facilitating a more targeted approach for the treatment of these disorders. Most of these newly identified pathogenic drivers of type 2 inflammation and their corresponding treatments are related to mast cells, eosinophils, T cells, B cells, epithelial cells and sensory nerves. Epithelial barrier defects and dysbiotic microbiomes represent exciting future drug targets for chronic type 2 inflammatory conditions. Here, we review common targets, current treatments and emerging therapies for the treatment of five major type 2 chronic inflammatory diseases — atopic dermatitis, chronic prurigo, chronic urticaria, asthma and chronic rhinosinusitis with nasal polyps — with a high need for targeted therapies. Unmet needs and future directions in the field are discussed.
Author(s)
Kolkhir, P. V.
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Akdiş, Cezmi A. A.
Universität Zürich
Akdiş, Mübeccel
Universität Zürich
Bachert, Claus
Universitätsklinikum Münster
Bieber, Thomas
Universitätsklinikum Bonn
Canonica, Walter G.
Humanitas University
Guttman-Yassky, Emma
Icahn School of Medicine at Mount Sinai
Metz, M.
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Mullol, Joaquim
Universitat de Barcelona
Palomares, Oscar
Universidad Complutense de Madrid
Renz, Harald E.
Universitätsklinikum Gießen und Marburg, Standort Marburg
Ständer, Sonja
Universitätsklinikum Münster
Zuberbier, Torsten
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Maurer, Marcus
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Journal
Nature Reviews Drug Discovery  
DOI
10.1038/s41573-023-00750-1
Language
English
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
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