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Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis

Mononuclear phagocytes (MPs) are important immune regulatory cells in atopic dermatitis (AD). We previously identified 6-sulfo LacNAc-expressing monocytes (slanMo) as TNF-α- and IL-23-producing cells in psoriatic skin lesions and as inducers of IFN-γ-, IL-17-, and IL-22-producing T cells. These cyto...

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Autores principales: Baran, Wojciech, Oehrl, Stephanie, Ahmad, Fareed, Döbel, Thomas, Alt, Christina, Buske-Kirschbaum, Angelika, Schmitz, Marc, Schäkel, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021776/
https://www.ncbi.nlm.nih.gov/pubmed/29977237
http://dx.doi.org/10.3389/fimmu.2018.01352
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author Baran, Wojciech
Oehrl, Stephanie
Ahmad, Fareed
Döbel, Thomas
Alt, Christina
Buske-Kirschbaum, Angelika
Schmitz, Marc
Schäkel, Knut
author_facet Baran, Wojciech
Oehrl, Stephanie
Ahmad, Fareed
Döbel, Thomas
Alt, Christina
Buske-Kirschbaum, Angelika
Schmitz, Marc
Schäkel, Knut
author_sort Baran, Wojciech
collection PubMed
description Mononuclear phagocytes (MPs) are important immune regulatory cells in atopic dermatitis (AD). We previously identified 6-sulfo LacNAc-expressing monocytes (slanMo) as TNF-α- and IL-23-producing cells in psoriatic skin lesions and as inducers of IFN-γ-, IL-17-, and IL-22-producing T cells. These cytokines are also upregulated in AD and normalize with treatment, as recently shown for dupilumab-treated patients. We here asked for the role of slanMo in AD. Increased numbers of slanMo were found in AD skin lesions. In difference to other MPs in AD, slanMo lacked expression of FcɛRI, CD1a, CD14, and CD163. slanMo from blood of patients with AD expressed increased levels of CD86 and produced IL-12 and TNF-α at higher amounts than CD14(+) monocytes and myeloid dendritic cells. While CD14(+) monocytes from patients with AD revealed a reduced IL-12 production, we observed no difference in the cytokine production comparing slanMo in AD and healthy controls. Interestingly, experimentally induced mental stress, a common trigger of flares in patients with AD, rapidly mobilized slanMo which retained their high TNF-α-producing capacity. This study identifies slanMo as a distinct population of inflammatory cells in skin lesions and as proinflammatory blood cells in patients with AD. slanMo may, therefore, represent a potent future target for treatment of AD.
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spelling pubmed-60217762018-07-05 Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis Baran, Wojciech Oehrl, Stephanie Ahmad, Fareed Döbel, Thomas Alt, Christina Buske-Kirschbaum, Angelika Schmitz, Marc Schäkel, Knut Front Immunol Immunology Mononuclear phagocytes (MPs) are important immune regulatory cells in atopic dermatitis (AD). We previously identified 6-sulfo LacNAc-expressing monocytes (slanMo) as TNF-α- and IL-23-producing cells in psoriatic skin lesions and as inducers of IFN-γ-, IL-17-, and IL-22-producing T cells. These cytokines are also upregulated in AD and normalize with treatment, as recently shown for dupilumab-treated patients. We here asked for the role of slanMo in AD. Increased numbers of slanMo were found in AD skin lesions. In difference to other MPs in AD, slanMo lacked expression of FcɛRI, CD1a, CD14, and CD163. slanMo from blood of patients with AD expressed increased levels of CD86 and produced IL-12 and TNF-α at higher amounts than CD14(+) monocytes and myeloid dendritic cells. While CD14(+) monocytes from patients with AD revealed a reduced IL-12 production, we observed no difference in the cytokine production comparing slanMo in AD and healthy controls. Interestingly, experimentally induced mental stress, a common trigger of flares in patients with AD, rapidly mobilized slanMo which retained their high TNF-α-producing capacity. This study identifies slanMo as a distinct population of inflammatory cells in skin lesions and as proinflammatory blood cells in patients with AD. slanMo may, therefore, represent a potent future target for treatment of AD. Frontiers Media S.A. 2018-06-21 /pmc/articles/PMC6021776/ /pubmed/29977237 http://dx.doi.org/10.3389/fimmu.2018.01352 Text en Copyright © 2018 Baran, Oehrl, Ahmad, Döbel, Alt, Buske-Kirschbaum, Schmitz and Schäkel. 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 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
Baran, Wojciech
Oehrl, Stephanie
Ahmad, Fareed
Döbel, Thomas
Alt, Christina
Buske-Kirschbaum, Angelika
Schmitz, Marc
Schäkel, Knut
Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title_full Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title_fullStr Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title_full_unstemmed Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title_short Phenotype, Function, and Mobilization of 6-Sulfo LacNAc-Expressing Monocytes in Atopic Dermatitis
title_sort phenotype, function, and mobilization of 6-sulfo lacnac-expressing monocytes in atopic dermatitis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021776/
https://www.ncbi.nlm.nih.gov/pubmed/29977237
http://dx.doi.org/10.3389/fimmu.2018.01352
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