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Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis
INTRODUCTION: Among the broad spectrum of cytokines, interleukin 1-β (IL-1β) has been implicated in induction and subsequent aggravation of skin lesions in atopic dermatitis (AD). A considerable body of evidence suggests that vitamin D status also influences the risk and/or severity of AD. MATERIAL...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Polish Society of Experimental and Clinical Immunology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102616/ https://www.ncbi.nlm.nih.gov/pubmed/30135631 http://dx.doi.org/10.5114/ceji.2018.77388 |
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author | Machura, Edyta Szczepańska, Maria Mazur, Bogdan Ziora, Katarzyna Kasperska-Zając, Alicja |
author_facet | Machura, Edyta Szczepańska, Maria Mazur, Bogdan Ziora, Katarzyna Kasperska-Zając, Alicja |
author_sort | Machura, Edyta |
collection | PubMed |
description | INTRODUCTION: Among the broad spectrum of cytokines, interleukin 1-β (IL-1β) has been implicated in induction and subsequent aggravation of skin lesions in atopic dermatitis (AD). A considerable body of evidence suggests that vitamin D status also influences the risk and/or severity of AD. MATERIAL AND METHODS: Fifty-seven children suffering from mild to severe AD were enrolled in the study. The control group consisted of 33 matched healthy children. In all the children serum concentrations of IL-1β/IL-1F2 and the interleukin-1 receptor antagonist IL-Ra/1F3 were measured. Serum 25(OH)D concentration was obtained for 49 patients with AD and all healthy children. RESULTS: In children with AD 59.2% of children had insufficiency, 24.5% had deficiency and 16.3% had a sufficient serum 25(OH)D level. In the control group 26.5%, 52.9% and 20% of participants had insufficiency/deficiency/sufficiency of 25(OH)D, respectively. The severity of AD was positively correlated with total IgE level, percentage and absolute count of eosinophils and IL-1Ra. IL-1β correlated with IL-1Ra. CONCLUSIONS: In children with AD the serum vitamin D level was lower than in healthy children. The correlation between severity of AD and IL-1Ra may prove that inflammasome-dependent IL-1β is involved in immunopathogenesis of the disease. Further studies are needed on a larger population of children to confirm the role of this cytokine in development of AD. |
format | Online Article Text |
id | pubmed-6102616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61026162018-08-22 Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis Machura, Edyta Szczepańska, Maria Mazur, Bogdan Ziora, Katarzyna Kasperska-Zając, Alicja Cent Eur J Immunol Clinical Immunology INTRODUCTION: Among the broad spectrum of cytokines, interleukin 1-β (IL-1β) has been implicated in induction and subsequent aggravation of skin lesions in atopic dermatitis (AD). A considerable body of evidence suggests that vitamin D status also influences the risk and/or severity of AD. MATERIAL AND METHODS: Fifty-seven children suffering from mild to severe AD were enrolled in the study. The control group consisted of 33 matched healthy children. In all the children serum concentrations of IL-1β/IL-1F2 and the interleukin-1 receptor antagonist IL-Ra/1F3 were measured. Serum 25(OH)D concentration was obtained for 49 patients with AD and all healthy children. RESULTS: In children with AD 59.2% of children had insufficiency, 24.5% had deficiency and 16.3% had a sufficient serum 25(OH)D level. In the control group 26.5%, 52.9% and 20% of participants had insufficiency/deficiency/sufficiency of 25(OH)D, respectively. The severity of AD was positively correlated with total IgE level, percentage and absolute count of eosinophils and IL-1Ra. IL-1β correlated with IL-1Ra. CONCLUSIONS: In children with AD the serum vitamin D level was lower than in healthy children. The correlation between severity of AD and IL-1Ra may prove that inflammasome-dependent IL-1β is involved in immunopathogenesis of the disease. Further studies are needed on a larger population of children to confirm the role of this cytokine in development of AD. Polish Society of Experimental and Clinical Immunology 2018-06-30 2018 /pmc/articles/PMC6102616/ /pubmed/30135631 http://dx.doi.org/10.5114/ceji.2018.77388 Text en Copyright: © 2018 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Immunology Machura, Edyta Szczepańska, Maria Mazur, Bogdan Ziora, Katarzyna Kasperska-Zając, Alicja Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title | Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title_full | Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title_fullStr | Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title_full_unstemmed | Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title_short | Interleukin 1-β, interleukin-1 receptor antagonist and vitamin D levels in children with atopic dermatitis |
title_sort | interleukin 1-β, interleukin-1 receptor antagonist and vitamin d levels in children with atopic dermatitis |
topic | Clinical Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102616/ https://www.ncbi.nlm.nih.gov/pubmed/30135631 http://dx.doi.org/10.5114/ceji.2018.77388 |
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