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Current and emerging biological therapy in adult-onset Still’s disease

Adult-onset Still’s disease (AOSD) is a rare, but characteristic non-familial, multi-genic systemic auto-inflammatory disorder, characterized by high spiking fever, salmon-like evanescent skin rash, polyarthritis, sore throat, hyperferritinemia and leucocytosis. The hallmark of AOSD is a cytokine st...

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Detalles Bibliográficos
Autores principales: Ma, Yuning, Meng, Jianfen, Jia, Jinchao, Wang, Mengyan, Teng, Jialin, Zhu, Dehao, Yang, Chengde, Hu, Qiongyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410009/
https://www.ncbi.nlm.nih.gov/pubmed/34117886
http://dx.doi.org/10.1093/rheumatology/keab485
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author Ma, Yuning
Meng, Jianfen
Jia, Jinchao
Wang, Mengyan
Teng, Jialin
Zhu, Dehao
Yang, Chengde
Hu, Qiongyi
author_facet Ma, Yuning
Meng, Jianfen
Jia, Jinchao
Wang, Mengyan
Teng, Jialin
Zhu, Dehao
Yang, Chengde
Hu, Qiongyi
author_sort Ma, Yuning
collection PubMed
description Adult-onset Still’s disease (AOSD) is a rare, but characteristic non-familial, multi-genic systemic auto-inflammatory disorder, characterized by high spiking fever, salmon-like evanescent skin rash, polyarthritis, sore throat, hyperferritinemia and leucocytosis. The hallmark of AOSD is a cytokine storm triggered by dysregulation of inflammation. Nowadays, with advances in anti-cytokine biologic agents, the treatment of AOSD is no longer limited to NSAIDs, glucocorticoids or conventional synthetic DMARDs. In this review, we focussed on the roles of these cytokines in the pathogenesis of AOSD and summarized the current and emerging biological therapy.
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spelling pubmed-84100092021-09-02 Current and emerging biological therapy in adult-onset Still’s disease Ma, Yuning Meng, Jianfen Jia, Jinchao Wang, Mengyan Teng, Jialin Zhu, Dehao Yang, Chengde Hu, Qiongyi Rheumatology (Oxford) Reviews Adult-onset Still’s disease (AOSD) is a rare, but characteristic non-familial, multi-genic systemic auto-inflammatory disorder, characterized by high spiking fever, salmon-like evanescent skin rash, polyarthritis, sore throat, hyperferritinemia and leucocytosis. The hallmark of AOSD is a cytokine storm triggered by dysregulation of inflammation. Nowadays, with advances in anti-cytokine biologic agents, the treatment of AOSD is no longer limited to NSAIDs, glucocorticoids or conventional synthetic DMARDs. In this review, we focussed on the roles of these cytokines in the pathogenesis of AOSD and summarized the current and emerging biological therapy. Oxford University Press 2021-06-12 /pmc/articles/PMC8410009/ /pubmed/34117886 http://dx.doi.org/10.1093/rheumatology/keab485 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, [br]distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Reviews
Ma, Yuning
Meng, Jianfen
Jia, Jinchao
Wang, Mengyan
Teng, Jialin
Zhu, Dehao
Yang, Chengde
Hu, Qiongyi
Current and emerging biological therapy in adult-onset Still’s disease
title Current and emerging biological therapy in adult-onset Still’s disease
title_full Current and emerging biological therapy in adult-onset Still’s disease
title_fullStr Current and emerging biological therapy in adult-onset Still’s disease
title_full_unstemmed Current and emerging biological therapy in adult-onset Still’s disease
title_short Current and emerging biological therapy in adult-onset Still’s disease
title_sort current and emerging biological therapy in adult-onset still’s disease
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410009/
https://www.ncbi.nlm.nih.gov/pubmed/34117886
http://dx.doi.org/10.1093/rheumatology/keab485
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