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Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis
Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by barrier dysfunction, dysregulated immune response, and dysbiosis with increased Staphylococcus aureus colonization. Infiltration of various T helper cell subsets into lesional skin and subsequent cytokine release are a ha...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022745/ https://www.ncbi.nlm.nih.gov/pubmed/35464457 http://dx.doi.org/10.3389/fimmu.2022.801579 |
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author | Humeau, Mélanie Boniface, Katia Bodet, Charles |
author_facet | Humeau, Mélanie Boniface, Katia Bodet, Charles |
author_sort | Humeau, Mélanie |
collection | PubMed |
description | Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by barrier dysfunction, dysregulated immune response, and dysbiosis with increased Staphylococcus aureus colonization. Infiltration of various T helper cell subsets into lesional skin and subsequent cytokine release are a hallmark of AD. Release of cytokines by both T cells and keratinocytes plays a key role in skin inflammation and drives many AD features. This review aims to discuss cytokine-mediated crosstalk between T cells and keratinocytes in AD pathogenesis and the potential impact of virulence factors produced by Staphylococcus aureus on these interactions. |
format | Online Article Text |
id | pubmed-9022745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90227452022-04-22 Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis Humeau, Mélanie Boniface, Katia Bodet, Charles Front Immunol Immunology Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by barrier dysfunction, dysregulated immune response, and dysbiosis with increased Staphylococcus aureus colonization. Infiltration of various T helper cell subsets into lesional skin and subsequent cytokine release are a hallmark of AD. Release of cytokines by both T cells and keratinocytes plays a key role in skin inflammation and drives many AD features. This review aims to discuss cytokine-mediated crosstalk between T cells and keratinocytes in AD pathogenesis and the potential impact of virulence factors produced by Staphylococcus aureus on these interactions. Frontiers Media S.A. 2022-04-07 /pmc/articles/PMC9022745/ /pubmed/35464457 http://dx.doi.org/10.3389/fimmu.2022.801579 Text en Copyright © 2022 Humeau, Boniface and Bodet https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Humeau, Mélanie Boniface, Katia Bodet, Charles Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title | Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title_full | Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title_fullStr | Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title_full_unstemmed | Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title_short | Cytokine-Mediated Crosstalk Between Keratinocytes and T Cells in Atopic Dermatitis |
title_sort | cytokine-mediated crosstalk between keratinocytes and t cells in atopic dermatitis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022745/ https://www.ncbi.nlm.nih.gov/pubmed/35464457 http://dx.doi.org/10.3389/fimmu.2022.801579 |
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