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The extracellular serine protease from Staphylococcus epidermidis elicits a type 2-biased immune response in atopic dermatitis patients
- Background Atopic dermatitis (AD) is a chronic, relapsing inflammatory skin disease with skin barrier defects and a misdirected type 2 immune response against harmless antigens. The skin microbiome in AD is characterized by a reduction in microbial diversity with a dominance of staphylococci, including Staphylococcus epidermidis ( S. epidermidis ). Objective To assess whether S. epidermidis antigens play a role in AD, we screened for candidate allergens and studied the T cell and humoral immune response against the extracellular serine protease (Esp). Methods To identify candidate allergens, we analyzed the binding of human serum IgG4, as a surrogate of IgE, to S. epidermidis extracellular proteins using 2-dimensional immunoblotting and mass spectrometry. We then measured serum IgE and IgG1 binding to recombinant Esp by ELISA in healthy and AD individuals. We also stimulated T cells from AD patients and control subjects with Esp and measured the secreted cytokines. Finally, we analyzed the proteolytic activity of Esp against IL-33 and determined the cleavage sites by mass spectrometry. Results We identified Esp as the dominant candidate allergen of S. epidermidis . Esp-specific IgE was present in human serum; AD patients had higher concentrations than controls. T cells reacting to Esp were detectable in both AD patients and healthy controls. The T cell response in healthy adults was characterized by IL-17, IL-22, IFN-γ, and IL-10, whereas the AD patients’ T cells lacked IL-17 production and released only low amounts of IL-22, IFN-γ, and IL-10. In contrast, Th2 cytokine release was higher in T cells from AD patients than from healthy controls. Mature Esp cleaved and activated the alarmin IL-33. Conclusion The extracellular serine protease Esp of S. epidermidis can activate IL-33. As an antigen, Esp elicits a type 2-biased antibody and T cell response in AD patients. This suggests that S. epidermidis can aggravate AD through the allergenic properties of Esp.
| Author: | Goran AbdurrahmanORCiD, Rebecca PospichORCiD, Leif SteilORCiD, Manuela Gesell Salazar, Juan José Izquierdo González, Nicole Normann, Daniel Mrochen, Christian ScharfORCiD, Uwe VölkerORCiD, Thomas Werfel, Barbara M. BrökerORCiD, Lennart M. RoesnerORCiD, Lidia Gómez-GascónORCiD |
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| URN: | urn:nbn:de:gbv:9-opus-111542 |
| DOI: | https://doi.org/10.3389/fimmu.2024.1352704 |
| ISSN: | 1664-3224 |
| Parent Title (English): | Frontiers in Immunology |
| Publisher: | Frontiers Media S.A. |
| Place of publication: | Lausanne |
| Document Type: | Article |
| Language: | English |
| Date of first Publication: | 2024/06/04 |
| Release Date: | 2025/04/11 |
| Tag: | Esp; IgE; Th2 cells; allergy; atopic dermatitis; protease |
| Volume: | 15 |
| Article Number: | 1352704 |
| Page Number: | 14 |
| Faculties: | Universitätsmedizin / Institut für Immunologie |
| Collections: | Artikel aus DFG-gefördertem Publikationsfonds |
| Licence (German): | Creative Commons - Namensnennung 4.0 International |

