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The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease

INTRODUCTION: Kawasaki disease (KD) is an acute febrile systemic vasculitis, but the etiology remains unknown. We studied serum levels of CD147, DcR3, and IL33 in different stages of KD to explore the value of CD147, DcR3, and IL33 in the pathophysiology of KD. METHODS: We measured serum levels of C...

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Autores principales: Qi, Yanqi, Xu, Jiawen, Lin, Zhe, Tao, Yijing, Zheng, Fenglei, Wang, Yujia, Sun, Yameng, Fu, Songling, Wang, Wei, Xie, Chunhong, Zhang, Yiying, Gong, Fangqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610753/
https://www.ncbi.nlm.nih.gov/pubmed/34824540
http://dx.doi.org/10.2147/JIR.S338763
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author Qi, Yanqi
Xu, Jiawen
Lin, Zhe
Tao, Yijing
Zheng, Fenglei
Wang, Yujia
Sun, Yameng
Fu, Songling
Wang, Wei
Xie, Chunhong
Zhang, Yiying
Gong, Fangqi
author_facet Qi, Yanqi
Xu, Jiawen
Lin, Zhe
Tao, Yijing
Zheng, Fenglei
Wang, Yujia
Sun, Yameng
Fu, Songling
Wang, Wei
Xie, Chunhong
Zhang, Yiying
Gong, Fangqi
author_sort Qi, Yanqi
collection PubMed
description INTRODUCTION: Kawasaki disease (KD) is an acute febrile systemic vasculitis, but the etiology remains unknown. We studied serum levels of CD147, DcR3, and IL33 in different stages of KD to explore the value of CD147, DcR3, and IL33 in the pathophysiology of KD. METHODS: We measured serum levels of CD147, DcR3, and IL33 by enzyme-linked immunosorbent assay (ELISA) at different stages with 71 KD patients and 66 healthy control children. We apply for network tools GeneMANIA and Cytoscape APP to analyze the functions of these pro-inflammatory factors at the gene and protein level. RESULTS: Serum levels of CD147, DcR3, and IL33 were significantly increased in KD patients before IVIG treatment. Serum levels of CD147, DcR3, and IL33 gradually decreased over time after the treatment of IVIG. Eight cases were IVIG non-responders, while nine KD patients got CALs, but they did not overlap. And there were no statistical differences between group IVIG responders and IVIG non-responders or between groups without CALs and with CALs. We explored the functions of CD147, DcR3, and IL33 from GeneMANIA and Cytoscape APP and found these third pro-inflammatory factors were coexpressed, physical interactions, genetic interactions with other KD-related factors. CONCLUSION: CD147, DcR3, and IL33 are involved in the pathophysiology of KD, which provides novel evidence for diagnosing and treating KD with their inhibitors.
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spelling pubmed-86107532021-11-24 The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease Qi, Yanqi Xu, Jiawen Lin, Zhe Tao, Yijing Zheng, Fenglei Wang, Yujia Sun, Yameng Fu, Songling Wang, Wei Xie, Chunhong Zhang, Yiying Gong, Fangqi J Inflamm Res Original Research INTRODUCTION: Kawasaki disease (KD) is an acute febrile systemic vasculitis, but the etiology remains unknown. We studied serum levels of CD147, DcR3, and IL33 in different stages of KD to explore the value of CD147, DcR3, and IL33 in the pathophysiology of KD. METHODS: We measured serum levels of CD147, DcR3, and IL33 by enzyme-linked immunosorbent assay (ELISA) at different stages with 71 KD patients and 66 healthy control children. We apply for network tools GeneMANIA and Cytoscape APP to analyze the functions of these pro-inflammatory factors at the gene and protein level. RESULTS: Serum levels of CD147, DcR3, and IL33 were significantly increased in KD patients before IVIG treatment. Serum levels of CD147, DcR3, and IL33 gradually decreased over time after the treatment of IVIG. Eight cases were IVIG non-responders, while nine KD patients got CALs, but they did not overlap. And there were no statistical differences between group IVIG responders and IVIG non-responders or between groups without CALs and with CALs. We explored the functions of CD147, DcR3, and IL33 from GeneMANIA and Cytoscape APP and found these third pro-inflammatory factors were coexpressed, physical interactions, genetic interactions with other KD-related factors. CONCLUSION: CD147, DcR3, and IL33 are involved in the pathophysiology of KD, which provides novel evidence for diagnosing and treating KD with their inhibitors. Dove 2021-11-19 /pmc/articles/PMC8610753/ /pubmed/34824540 http://dx.doi.org/10.2147/JIR.S338763 Text en © 2021 Qi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Qi, Yanqi
Xu, Jiawen
Lin, Zhe
Tao, Yijing
Zheng, Fenglei
Wang, Yujia
Sun, Yameng
Fu, Songling
Wang, Wei
Xie, Chunhong
Zhang, Yiying
Gong, Fangqi
The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title_full The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title_fullStr The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title_full_unstemmed The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title_short The Network of Pro-Inflammatory Factors CD147, DcR3, and IL33 in the Development of Kawasaki Disease
title_sort network of pro-inflammatory factors cd147, dcr3, and il33 in the development of kawasaki disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610753/
https://www.ncbi.nlm.nih.gov/pubmed/34824540
http://dx.doi.org/10.2147/JIR.S338763
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