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Advances and challenges in targeting IRF5, a key regulator of inflammation

Interferon regulatory factor 5 (IRF5) belongs to a family of transcription factors, originally implicated in antiviral responses and interferon production. However, studies conducted in different laboratories over the last decade have placed IRF5 as a central regulator of the inflammatory response....

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Detalles Bibliográficos
Autores principales: Almuttaqi, Hannah, Udalova, Irina A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563445/
https://www.ncbi.nlm.nih.gov/pubmed/30199605
http://dx.doi.org/10.1111/febs.14654
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author Almuttaqi, Hannah
Udalova, Irina A.
author_facet Almuttaqi, Hannah
Udalova, Irina A.
author_sort Almuttaqi, Hannah
collection PubMed
description Interferon regulatory factor 5 (IRF5) belongs to a family of transcription factors, originally implicated in antiviral responses and interferon production. However, studies conducted in different laboratories over the last decade have placed IRF5 as a central regulator of the inflammatory response. It has become clear that IRF5 contributes to the pathogenesis of many inflammatory and autoimmune diseases, such as rheumatoid arthritis, inflammatory bowel disease and systemic lupus erythematosus. Given the role of IRF5 in physiology and disease, IRF5 represents a potential therapeutic target. However, despite a significant interest from the pharmaceutical industry, inhibitors that interfere with the IRF5 pathway remain elusive. Here, we review the advances made by various studies in targeting multiple steps of signalling leading to IRF5 activation with their therapeutic potential, and the possible complications of such strategies are discussed.
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spelling pubmed-65634452019-06-17 Advances and challenges in targeting IRF5, a key regulator of inflammation Almuttaqi, Hannah Udalova, Irina A. FEBS J Review Article Interferon regulatory factor 5 (IRF5) belongs to a family of transcription factors, originally implicated in antiviral responses and interferon production. However, studies conducted in different laboratories over the last decade have placed IRF5 as a central regulator of the inflammatory response. It has become clear that IRF5 contributes to the pathogenesis of many inflammatory and autoimmune diseases, such as rheumatoid arthritis, inflammatory bowel disease and systemic lupus erythematosus. Given the role of IRF5 in physiology and disease, IRF5 represents a potential therapeutic target. However, despite a significant interest from the pharmaceutical industry, inhibitors that interfere with the IRF5 pathway remain elusive. Here, we review the advances made by various studies in targeting multiple steps of signalling leading to IRF5 activation with their therapeutic potential, and the possible complications of such strategies are discussed. John Wiley and Sons Inc. 2018-09-21 2019-05 /pmc/articles/PMC6563445/ /pubmed/30199605 http://dx.doi.org/10.1111/febs.14654 Text en © 2018 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Almuttaqi, Hannah
Udalova, Irina A.
Advances and challenges in targeting IRF5, a key regulator of inflammation
title Advances and challenges in targeting IRF5, a key regulator of inflammation
title_full Advances and challenges in targeting IRF5, a key regulator of inflammation
title_fullStr Advances and challenges in targeting IRF5, a key regulator of inflammation
title_full_unstemmed Advances and challenges in targeting IRF5, a key regulator of inflammation
title_short Advances and challenges in targeting IRF5, a key regulator of inflammation
title_sort advances and challenges in targeting irf5, a key regulator of inflammation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563445/
https://www.ncbi.nlm.nih.gov/pubmed/30199605
http://dx.doi.org/10.1111/febs.14654
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