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The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
Interleukin-17 (IL-17) is an essential proinflammatory cytokine, which is mainly secreted by the CD4(+) helper T cells (Th17 cells) and subsets of innate lymphoid cells. IL-17A is associated with the pathogenesis of inflammatory diseases, including psoriasis, atopic dermatitis, hidradenitis suppurat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705238/ https://www.ncbi.nlm.nih.gov/pubmed/33281823 http://dx.doi.org/10.3389/fimmu.2020.594735 |
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author | Liu, Taoming Li, Sheng Ying, Shuni Tang, Shunli Ding, Yuwei Li, Yali Qiao, Jianjun Fang, Hong |
author_facet | Liu, Taoming Li, Sheng Ying, Shuni Tang, Shunli Ding, Yuwei Li, Yali Qiao, Jianjun Fang, Hong |
author_sort | Liu, Taoming |
collection | PubMed |
description | Interleukin-17 (IL-17) is an essential proinflammatory cytokine, which is mainly secreted by the CD4(+) helper T cells (Th17 cells) and subsets of innate lymphoid cells. IL-17A is associated with the pathogenesis of inflammatory diseases, including psoriasis, atopic dermatitis, hidradenitis suppurativa, alopecia areata, pityriasis rubra pilaris, pemphigus, and systemic sclerosis. Interleukin-23 (IL-23) plays a pivotal role in stimulating the production of IL-17 by activating the Th17 cells. The IL-23/IL-17 axis is an important pathway for targeted therapy for inflammatory diseases. Emerging evidence from clinical trials has shown that monoclonal antibodies against IL-23, IL-17, and tumor necrosis factor are effective in the treatment of patients with psoriasis, atopic dermatitis, hidradenitis suppurativa, pityriasis rubra pilaris, pemphigus, and systemic sclerosis. Here, we summarize the latest knowledge about the biology, signaling, and pathophysiological functions of the IL-23/IL-17 axis in inflammatory skin diseases. The currently available biologics targeting the axis is also discussed. |
format | Online Article Text |
id | pubmed-7705238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77052382020-12-03 The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside Liu, Taoming Li, Sheng Ying, Shuni Tang, Shunli Ding, Yuwei Li, Yali Qiao, Jianjun Fang, Hong Front Immunol Immunology Interleukin-17 (IL-17) is an essential proinflammatory cytokine, which is mainly secreted by the CD4(+) helper T cells (Th17 cells) and subsets of innate lymphoid cells. IL-17A is associated with the pathogenesis of inflammatory diseases, including psoriasis, atopic dermatitis, hidradenitis suppurativa, alopecia areata, pityriasis rubra pilaris, pemphigus, and systemic sclerosis. Interleukin-23 (IL-23) plays a pivotal role in stimulating the production of IL-17 by activating the Th17 cells. The IL-23/IL-17 axis is an important pathway for targeted therapy for inflammatory diseases. Emerging evidence from clinical trials has shown that monoclonal antibodies against IL-23, IL-17, and tumor necrosis factor are effective in the treatment of patients with psoriasis, atopic dermatitis, hidradenitis suppurativa, pityriasis rubra pilaris, pemphigus, and systemic sclerosis. Here, we summarize the latest knowledge about the biology, signaling, and pathophysiological functions of the IL-23/IL-17 axis in inflammatory skin diseases. The currently available biologics targeting the axis is also discussed. Frontiers Media S.A. 2020-11-17 /pmc/articles/PMC7705238/ /pubmed/33281823 http://dx.doi.org/10.3389/fimmu.2020.594735 Text en Copyright © 2020 Liu, Li, Ying, Tang, Ding, Li, Qiao and Fang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Liu, Taoming Li, Sheng Ying, Shuni Tang, Shunli Ding, Yuwei Li, Yali Qiao, Jianjun Fang, Hong The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title | The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title_full | The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title_fullStr | The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title_full_unstemmed | The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title_short | The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside |
title_sort | il-23/il-17 pathway in inflammatory skin diseases: from bench to bedside |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705238/ https://www.ncbi.nlm.nih.gov/pubmed/33281823 http://dx.doi.org/10.3389/fimmu.2020.594735 |
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