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IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants

Psoriasis vulgaris (PV) is a cutaneous inflammatory disorder stemming from abnormal, persistent activation of the interleukin- (IL-)23/Th17 axis. Pustular psoriasis (PP) is a clinicopathological variant of psoriasis, histopathologically defined by the predominance of intraepidermal collections of ne...

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Autores principales: Saggini, Andrea, Chimenti, Sergio, Chiricozzi, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122019/
https://www.ncbi.nlm.nih.gov/pubmed/25126586
http://dx.doi.org/10.1155/2014/964069
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author Saggini, Andrea
Chimenti, Sergio
Chiricozzi, Andrea
author_facet Saggini, Andrea
Chimenti, Sergio
Chiricozzi, Andrea
author_sort Saggini, Andrea
collection PubMed
description Psoriasis vulgaris (PV) is a cutaneous inflammatory disorder stemming from abnormal, persistent activation of the interleukin- (IL-)23/Th17 axis. Pustular psoriasis (PP) is a clinicopathological variant of psoriasis, histopathologically defined by the predominance of intraepidermal collections of neutrophils. Although PP pathogenesis is thought to largely follow that of (PV), recent evidences point to a more central role for IL-1, IL-36, and IL-6 in the development of PP. We review the role of IL-6 in the pathogenesis of PV and PP, focusing on its cross-talk with cytokines of the IL-23/Th17 axis. Clinical inhibitors of IL-6 signaling, including tocilizumab, have shown significant effectiveness in the treatment of several inflammatory rheumatic diseases, including rheumatoid arthritis and juvenile idiopathic arthritis; accordingly, anti-IL-6 agents may potentially represent future promising therapies for the treatment of PP.
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spelling pubmed-41220192014-08-14 IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants Saggini, Andrea Chimenti, Sergio Chiricozzi, Andrea J Immunol Res Review Article Psoriasis vulgaris (PV) is a cutaneous inflammatory disorder stemming from abnormal, persistent activation of the interleukin- (IL-)23/Th17 axis. Pustular psoriasis (PP) is a clinicopathological variant of psoriasis, histopathologically defined by the predominance of intraepidermal collections of neutrophils. Although PP pathogenesis is thought to largely follow that of (PV), recent evidences point to a more central role for IL-1, IL-36, and IL-6 in the development of PP. We review the role of IL-6 in the pathogenesis of PV and PP, focusing on its cross-talk with cytokines of the IL-23/Th17 axis. Clinical inhibitors of IL-6 signaling, including tocilizumab, have shown significant effectiveness in the treatment of several inflammatory rheumatic diseases, including rheumatoid arthritis and juvenile idiopathic arthritis; accordingly, anti-IL-6 agents may potentially represent future promising therapies for the treatment of PP. Hindawi Publishing Corporation 2014 2014-07-13 /pmc/articles/PMC4122019/ /pubmed/25126586 http://dx.doi.org/10.1155/2014/964069 Text en Copyright © 2014 Andrea Saggini et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Saggini, Andrea
Chimenti, Sergio
Chiricozzi, Andrea
IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title_full IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title_fullStr IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title_full_unstemmed IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title_short IL-6 as a Druggable Target in Psoriasis: Focus on Pustular Variants
title_sort il-6 as a druggable target in psoriasis: focus on pustular variants
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122019/
https://www.ncbi.nlm.nih.gov/pubmed/25126586
http://dx.doi.org/10.1155/2014/964069
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