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Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis
Eosinophilic esophagitis is a T-cell-driven allergic condition hallmarked by eosinophil infiltration of the esophagus. Eosinophils exposed to proliferating T cells release galectin-10 and have T-cell suppressive function in vitro. The aims of this study were to evaluate if eosinophils co-localize wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10128161/ https://www.ncbi.nlm.nih.gov/pubmed/36808213 http://dx.doi.org/10.1093/cei/uxad026 |
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author | Albinsson, Sofie Lingblom, Christine Johansson, Leif Larsson, Helen Wennerås, Christine |
author_facet | Albinsson, Sofie Lingblom, Christine Johansson, Leif Larsson, Helen Wennerås, Christine |
author_sort | Albinsson, Sofie |
collection | PubMed |
description | Eosinophilic esophagitis is a T-cell-driven allergic condition hallmarked by eosinophil infiltration of the esophagus. Eosinophils exposed to proliferating T cells release galectin-10 and have T-cell suppressive function in vitro. The aims of this study were to evaluate if eosinophils co-localize with T cells and release galectin-10 in the esophagus of patients with eosinophilic esophagitis. Esophageal biopsies from 20 patients with eosinophilic esophagitis were stained for major basic protein, galectin-10, CD4, CD8, CD16, and CD81 and analyzed by immunofluorescence confocal microscopy before and after topical corticosteroid treatment. CD4+ T-cell numbers decreased in the esophageal mucosa of responders to treatment but not in the non-responders. Suppressive (CD16+) eosinophils were present in the esophageal mucosa of patients with active disease and decreased after successful treatment. Unexpectedly, eosinophils and T cells were not in direct contact with each other. Instead, the esophageal eosinophils released large amounts of galectin-10-containing extracellular vesicles and featured cytoplasmic projections that contained galectin-10, both of which disappeared from the esophagus of the responders but remained in the non-responders. To conclude, the presence of CD16+ eosinophils together with the massive release of galectin-10-containing extracellular vesicles in the esophageal mucosa might indicate that eosinophils exert T-cell suppression in eosinophilic esophagitis. |
format | Online Article Text |
id | pubmed-10128161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101281612023-04-26 Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis Albinsson, Sofie Lingblom, Christine Johansson, Leif Larsson, Helen Wennerås, Christine Clin Exp Immunol Allergy and Asthma Eosinophilic esophagitis is a T-cell-driven allergic condition hallmarked by eosinophil infiltration of the esophagus. Eosinophils exposed to proliferating T cells release galectin-10 and have T-cell suppressive function in vitro. The aims of this study were to evaluate if eosinophils co-localize with T cells and release galectin-10 in the esophagus of patients with eosinophilic esophagitis. Esophageal biopsies from 20 patients with eosinophilic esophagitis were stained for major basic protein, galectin-10, CD4, CD8, CD16, and CD81 and analyzed by immunofluorescence confocal microscopy before and after topical corticosteroid treatment. CD4+ T-cell numbers decreased in the esophageal mucosa of responders to treatment but not in the non-responders. Suppressive (CD16+) eosinophils were present in the esophageal mucosa of patients with active disease and decreased after successful treatment. Unexpectedly, eosinophils and T cells were not in direct contact with each other. Instead, the esophageal eosinophils released large amounts of galectin-10-containing extracellular vesicles and featured cytoplasmic projections that contained galectin-10, both of which disappeared from the esophagus of the responders but remained in the non-responders. To conclude, the presence of CD16+ eosinophils together with the massive release of galectin-10-containing extracellular vesicles in the esophageal mucosa might indicate that eosinophils exert T-cell suppression in eosinophilic esophagitis. Oxford University Press 2023-02-20 /pmc/articles/PMC10128161/ /pubmed/36808213 http://dx.doi.org/10.1093/cei/uxad026 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Allergy and Asthma Albinsson, Sofie Lingblom, Christine Johansson, Leif Larsson, Helen Wennerås, Christine Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title | Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title_full | Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title_fullStr | Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title_full_unstemmed | Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title_short | Extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
title_sort | extracellular distribution of galectin-10 in the esophageal mucosa of patients with eosinophilic esophagitis |
topic | Allergy and Asthma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10128161/ https://www.ncbi.nlm.nih.gov/pubmed/36808213 http://dx.doi.org/10.1093/cei/uxad026 |
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