Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances
Chronic spontaneous urticaria (CSU) is a debilitating skin disease characterized by intensely itchy wheals, angioedema, or both. Symptoms recur spontaneously, on a near-daily basis, over >6 weeks; many patients experience flare-ups over several years and, consequently, reduced quality of life...
| Autores: | , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2023 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/55824 |
| Acceso en línea: | http://hdl.handle.net/10230/55824 http://dx.doi.org/10.1111/all.15603 |
| Access Level: | acceso abierto |
| Palabra clave: | IgE Angioedema Dermatology Mast cells Urticaria |
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Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advancesKaplan, Allen P.Lebwohl, MarkGiménez Arnau, Anna MariaHide, MichihiroArmstrong, April W.Maurer, MarcusIgEAngioedemaDermatologyMast cellsUrticariaChronic spontaneous urticaria (CSU) is a debilitating skin disease characterized by intensely itchy wheals, angioedema, or both. Symptoms recur spontaneously, on a near-daily basis, over >6 weeks; many patients experience flare-ups over several years and, consequently, reduced quality of life. Differences between the inflammatory profiles of the skin of CSU patients (wheals and nonlesional sites) and healthy controls indicate that key drivers such as mast cells, eosinophils, and basophils interact, release vasoactive mediators, and prime the skin, leaving patients predisposed to symptoms. Many cytokines and chemokines involved in these inflammatory networks and their corresponding intracellular signaling cascades have been identified. These insights informed the development of therapies such as omalizumab, dupilumab, and Bruton's tyrosine kinase (BTK) inhibitors, marking a renewed focus on pathogenesis in CSU clinical research. Despite progress, current therapies provide symptomatic control but do not appear to redress the inflammatory balance in the skin permanently. A deeper understanding of CSU pathogenesis will permit a more targeted approach to developing novel treatments with curative intent. Here, we review what is known about the pathogenesis of CSU and consider how this can be used to identify rational targets to improve patient care further.Wiley202320232023info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/55824http://dx.doi.org/10.1111/all.15603reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License http://creativecommons.org/licenses/by-nc/4.0/, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.© 2022 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.http://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/558242026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| title |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| spellingShingle |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances Kaplan, Allen P. IgE Angioedema Dermatology Mast cells Urticaria |
| title_short |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| title_full |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| title_fullStr |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| title_full_unstemmed |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| title_sort |
Chronic spontaneous urticaria. Focus on pathophysiology to unlock treatment advances |
| dc.creator.none.fl_str_mv |
Kaplan, Allen P. Lebwohl, Mark Giménez Arnau, Anna Maria Hide, Michihiro Armstrong, April W. Maurer, Marcus |
| author |
Kaplan, Allen P. |
| author_facet |
Kaplan, Allen P. Lebwohl, Mark Giménez Arnau, Anna Maria Hide, Michihiro Armstrong, April W. Maurer, Marcus |
| author_role |
author |
| author2 |
Lebwohl, Mark Giménez Arnau, Anna Maria Hide, Michihiro Armstrong, April W. Maurer, Marcus |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
IgE Angioedema Dermatology Mast cells Urticaria |
| topic |
IgE Angioedema Dermatology Mast cells Urticaria |
| description |
Chronic spontaneous urticaria (CSU) is a debilitating skin disease characterized by intensely itchy wheals, angioedema, or both. Symptoms recur spontaneously, on a near-daily basis, over >6 weeks; many patients experience flare-ups over several years and, consequently, reduced quality of life. Differences between the inflammatory profiles of the skin of CSU patients (wheals and nonlesional sites) and healthy controls indicate that key drivers such as mast cells, eosinophils, and basophils interact, release vasoactive mediators, and prime the skin, leaving patients predisposed to symptoms. Many cytokines and chemokines involved in these inflammatory networks and their corresponding intracellular signaling cascades have been identified. These insights informed the development of therapies such as omalizumab, dupilumab, and Bruton's tyrosine kinase (BTK) inhibitors, marking a renewed focus on pathogenesis in CSU clinical research. Despite progress, current therapies provide symptomatic control but do not appear to redress the inflammatory balance in the skin permanently. A deeper understanding of CSU pathogenesis will permit a more targeted approach to developing novel treatments with curative intent. Here, we review what is known about the pathogenesis of CSU and consider how this can be used to identify rational targets to improve patient care further. |
| publishDate |
2023 |
| dc.date.none.fl_str_mv |
2023 2023 2023 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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http://hdl.handle.net/10230/55824 http://dx.doi.org/10.1111/all.15603 |
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http://hdl.handle.net/10230/55824 http://dx.doi.org/10.1111/all.15603 |
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Inglés |
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Inglés |
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http://creativecommons.org/licenses/by-nc/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by-nc/4.0/ |
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openAccess |
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application/pdf application/pdf |
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Wiley |
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Wiley |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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