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Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment

The IL-17 cytokine family comprising IL-17A to IL-17F and receptor subunits IL-17RA to IL-17RE represents a genetically ancient intercellular network regulating local tissue homeostasis. Its pivotal role in antifungal defense and its central position in the pathogenesis of inflammatory diseases incl...

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Detalles Bibliográficos
Autores principales: Prinz, Immo, Sandrock, Inga, Mrowietz, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037256/
https://www.ncbi.nlm.nih.gov/pubmed/31727784
http://dx.doi.org/10.1084/jem.20191397
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author Prinz, Immo
Sandrock, Inga
Mrowietz, Ulrich
author_facet Prinz, Immo
Sandrock, Inga
Mrowietz, Ulrich
author_sort Prinz, Immo
collection PubMed
description The IL-17 cytokine family comprising IL-17A to IL-17F and receptor subunits IL-17RA to IL-17RE represents a genetically ancient intercellular network regulating local tissue homeostasis. Its pivotal role in antifungal defense and its central position in the pathogenesis of inflammatory diseases including psoriasis were discovered only relatively late in the early 2000s. Since the connection of dysregulated IL-17 and psoriasis pathogenesis turned out to be particularly evident, a number of monoclonal antibodies targeting IL-17 pathways have been approved and are used as first line treatment of moderate-to-severe plaque psoriasis and psoriatic arthritis, and further agents are currently in clinical development.
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spelling pubmed-70372562020-07-06 Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment Prinz, Immo Sandrock, Inga Mrowietz, Ulrich J Exp Med Reviews The IL-17 cytokine family comprising IL-17A to IL-17F and receptor subunits IL-17RA to IL-17RE represents a genetically ancient intercellular network regulating local tissue homeostasis. Its pivotal role in antifungal defense and its central position in the pathogenesis of inflammatory diseases including psoriasis were discovered only relatively late in the early 2000s. Since the connection of dysregulated IL-17 and psoriasis pathogenesis turned out to be particularly evident, a number of monoclonal antibodies targeting IL-17 pathways have been approved and are used as first line treatment of moderate-to-severe plaque psoriasis and psoriatic arthritis, and further agents are currently in clinical development. Rockefeller University Press 2019-11-14 /pmc/articles/PMC7037256/ /pubmed/31727784 http://dx.doi.org/10.1084/jem.20191397 Text en © 2019 Prinz et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Prinz, Immo
Sandrock, Inga
Mrowietz, Ulrich
Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title_full Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title_fullStr Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title_full_unstemmed Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title_short Interleukin-17 cytokines: Effectors and targets in psoriasis—A breakthrough in understanding and treatment
title_sort interleukin-17 cytokines: effectors and targets in psoriasis—a breakthrough in understanding and treatment
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037256/
https://www.ncbi.nlm.nih.gov/pubmed/31727784
http://dx.doi.org/10.1084/jem.20191397
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