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Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo

INTRODUCTION: Alopecia areata (AA) and vitiligo are both skin diseases of autoimmune origin. AA is characterized by patchy hair loss primarily on the scalp but may involve other areas as well, while vitiligo is caused by the destruction of melanocytes and results in the appearance of white patches o...

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Autores principales: Tomaszewska, Katarzyna A., Kozłowska, Magdalena, Kaszuba, Andrzej, Lesiak, Aleksandra, Narbutt, Joanna, Zalewska-Janowska, Anna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953894/
https://www.ncbi.nlm.nih.gov/pubmed/35369638
http://dx.doi.org/10.5114/ada.2022.113612
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author Tomaszewska, Katarzyna A.
Kozłowska, Magdalena
Kaszuba, Andrzej
Lesiak, Aleksandra
Narbutt, Joanna
Zalewska-Janowska, Anna M.
author_facet Tomaszewska, Katarzyna A.
Kozłowska, Magdalena
Kaszuba, Andrzej
Lesiak, Aleksandra
Narbutt, Joanna
Zalewska-Janowska, Anna M.
author_sort Tomaszewska, Katarzyna A.
collection PubMed
description INTRODUCTION: Alopecia areata (AA) and vitiligo are both skin diseases of autoimmune origin. AA is characterized by patchy hair loss primarily on the scalp but may involve other areas as well, while vitiligo is caused by the destruction of melanocytes and results in the appearance of white patches on any part of the body. Many facts indicate similar pathogenesis of these diseases. Both dermatoses are associated with frequent coexistence of other autoimmune diseases and share common genetic risk factors. Recent data support the theory of the involvement of IL-17 in the pathogenesis of both AA and vitiligo. AIM: To evaluate and compare the serum levels of interleukin (IL)-17 in patients with AA and non-segmental vitiligo (NSV). To assess whether the pattern of serum cytokine concentration can be associated with clinical details and activity of the disease. MATERIAL AND METHODS: A cross-sectional study was conducted on 33 patients with AA, 30 patients with NSV, and 30 healthy controls. Serum levels of IL-17 were determined quantitatively by ELISA method. RESULTS: Our analysis identified a systemic inflammatory signature associated with AA and NSV, characterized by elevated levels of IL-17. The levels of IL-17 did not differ significantly between AA patients and NSV patients. CONCLUSIONS: Our results show that AA and vitiligo may share common etiopathogenetic pathways, which suggests the potential of developing targeted therapies for both AA and vitiligo treatment. Imbalance of T cell subpopulations and complex systemic cytokine profiles may contribute to the pathogenesis of AA and vitiligo.
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spelling pubmed-89538942022-03-31 Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo Tomaszewska, Katarzyna A. Kozłowska, Magdalena Kaszuba, Andrzej Lesiak, Aleksandra Narbutt, Joanna Zalewska-Janowska, Anna M. Postepy Dermatol Alergol Original Paper INTRODUCTION: Alopecia areata (AA) and vitiligo are both skin diseases of autoimmune origin. AA is characterized by patchy hair loss primarily on the scalp but may involve other areas as well, while vitiligo is caused by the destruction of melanocytes and results in the appearance of white patches on any part of the body. Many facts indicate similar pathogenesis of these diseases. Both dermatoses are associated with frequent coexistence of other autoimmune diseases and share common genetic risk factors. Recent data support the theory of the involvement of IL-17 in the pathogenesis of both AA and vitiligo. AIM: To evaluate and compare the serum levels of interleukin (IL)-17 in patients with AA and non-segmental vitiligo (NSV). To assess whether the pattern of serum cytokine concentration can be associated with clinical details and activity of the disease. MATERIAL AND METHODS: A cross-sectional study was conducted on 33 patients with AA, 30 patients with NSV, and 30 healthy controls. Serum levels of IL-17 were determined quantitatively by ELISA method. RESULTS: Our analysis identified a systemic inflammatory signature associated with AA and NSV, characterized by elevated levels of IL-17. The levels of IL-17 did not differ significantly between AA patients and NSV patients. CONCLUSIONS: Our results show that AA and vitiligo may share common etiopathogenetic pathways, which suggests the potential of developing targeted therapies for both AA and vitiligo treatment. Imbalance of T cell subpopulations and complex systemic cytokine profiles may contribute to the pathogenesis of AA and vitiligo. Termedia Publishing House 2022-02-28 2022-02 /pmc/articles/PMC8953894/ /pubmed/35369638 http://dx.doi.org/10.5114/ada.2022.113612 Text en Copyright © 2022 Termedia https://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 (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) )
spellingShingle Original Paper
Tomaszewska, Katarzyna A.
Kozłowska, Magdalena
Kaszuba, Andrzej
Lesiak, Aleksandra
Narbutt, Joanna
Zalewska-Janowska, Anna M.
Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title_full Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title_fullStr Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title_full_unstemmed Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title_short Increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
title_sort increased serum levels of interleukin-17 in patients with alopecia areata and non-segmental vitiligo
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953894/
https://www.ncbi.nlm.nih.gov/pubmed/35369638
http://dx.doi.org/10.5114/ada.2022.113612
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