Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis
Jane Yoo,1 Anne M Manicone,2 John K McGuire,3 Ying Wang,2 William C Parks2 1Center for Lung Biology, Department of Medicine, Division of Dermatology, 2Division of Pulmonary and Critical Care Medicine, 3Department of Pediatrics, Division Critical Care Medicine, University of Washington, Seattle, WA,...
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Dove Medical Press
2014
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oai:doaj.org-article:9685841f6eb34600af78dc452526f08f2021-12-02T00:24:39ZSystemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis1178-7031https://doaj.org/article/9685841f6eb34600af78dc452526f08f2014-02-01T00:00:00Zhttp://www.dovepress.com/systemic-sensitization-with-the-protein-allergen-ovalbumin-augments-lo-a15900https://doaj.org/toc/1178-7031 Jane Yoo,1 Anne M Manicone,2 John K McGuire,3 Ying Wang,2 William C Parks2 1Center for Lung Biology, Department of Medicine, Division of Dermatology, 2Division of Pulmonary and Critical Care Medicine, 3Department of Pediatrics, Division Critical Care Medicine, University of Washington, Seattle, WA, USA Abstract: Mouse models of atopic dermatitis based on epicutaneous sensitization have shed light on the role of epicutaneous allergen entry in the development of respiratory and gastrointestinal allergy. However, the contribution of non-cutaneous modes of sensitization to skin diseases has not been evaluated. We assessed if systemic ovalbumin administration, in conjunction with local sensitization, could prime for a robust inflammatory response. Furthermore, we attempted to elucidate important aspects of disease pathogenesis previously unaddressed in mouse models. Mice that underwent intraperitoneal ovalbumin sensitization prior to epicutaneous challenge demonstrated an acute (Th2-polarized) atopic dermatitis-like phenotype upon local challenge. The inflammatory response was strikingly more robust than in mice that underwent epicutaneous sensitization alone. The lesional infiltrate contained a dendritic cell population that corresponded phenotypically with inflammatory dendritic epidermal cells of significance in human disease. Finally, in accordance with observations in human atopic dermatitis, there was an increase in cluster of differentiation (CD) 103 (αE subunit)-expressing CD4+ T lymphocytes. However, the absence of CD103 on approximately 50% of infiltrating cells argues against a primary role for the αEβ7 integrin in tissue homing. In conclusion, we present a mouse model of atopic dermatitis that reveals novel insights into the pathogenesis of this complex disease. Keywords: atopic dermatitis, mouse model, ovalbumin, sensitization, Th2, dendritic cellsYoo JManicone AMMcGuire JKWang YParks WCDove Medical PressarticlePathologyRB1-214Therapeutics. PharmacologyRM1-950ENJournal of Inflammation Research, Vol 2014, Iss default, Pp 29-38 (2014) |
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Pathology RB1-214 Therapeutics. Pharmacology RM1-950 |
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Pathology RB1-214 Therapeutics. Pharmacology RM1-950 Yoo J Manicone AM McGuire JK Wang Y Parks WC Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
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Jane Yoo,1 Anne M Manicone,2 John K McGuire,3 Ying Wang,2 William C Parks2 1Center for Lung Biology, Department of Medicine, Division of Dermatology, 2Division of Pulmonary and Critical Care Medicine, 3Department of Pediatrics, Division Critical Care Medicine, University of Washington, Seattle, WA, USA Abstract: Mouse models of atopic dermatitis based on epicutaneous sensitization have shed light on the role of epicutaneous allergen entry in the development of respiratory and gastrointestinal allergy. However, the contribution of non-cutaneous modes of sensitization to skin diseases has not been evaluated. We assessed if systemic ovalbumin administration, in conjunction with local sensitization, could prime for a robust inflammatory response. Furthermore, we attempted to elucidate important aspects of disease pathogenesis previously unaddressed in mouse models. Mice that underwent intraperitoneal ovalbumin sensitization prior to epicutaneous challenge demonstrated an acute (Th2-polarized) atopic dermatitis-like phenotype upon local challenge. The inflammatory response was strikingly more robust than in mice that underwent epicutaneous sensitization alone. The lesional infiltrate contained a dendritic cell population that corresponded phenotypically with inflammatory dendritic epidermal cells of significance in human disease. Finally, in accordance with observations in human atopic dermatitis, there was an increase in cluster of differentiation (CD) 103 (αE subunit)-expressing CD4+ T lymphocytes. However, the absence of CD103 on approximately 50% of infiltrating cells argues against a primary role for the αEβ7 integrin in tissue homing. In conclusion, we present a mouse model of atopic dermatitis that reveals novel insights into the pathogenesis of this complex disease. Keywords: atopic dermatitis, mouse model, ovalbumin, sensitization, Th2, dendritic cells |
format |
article |
author |
Yoo J Manicone AM McGuire JK Wang Y Parks WC |
author_facet |
Yoo J Manicone AM McGuire JK Wang Y Parks WC |
author_sort |
Yoo J |
title |
Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
title_short |
Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
title_full |
Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
title_fullStr |
Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
title_full_unstemmed |
Systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
title_sort |
systemic sensitization with the protein allergen ovalbumin augments local sensitization in atopic dermatitis |
publisher |
Dove Medical Press |
publishDate |
2014 |
url |
https://doaj.org/article/9685841f6eb34600af78dc452526f08f |
work_keys_str_mv |
AT yooj systemicsensitizationwiththeproteinallergenovalbuminaugmentslocalsensitizationinatopicdermatitis AT maniconeam systemicsensitizationwiththeproteinallergenovalbuminaugmentslocalsensitizationinatopicdermatitis AT mcguirejk systemicsensitizationwiththeproteinallergenovalbuminaugmentslocalsensitizationinatopicdermatitis AT wangy systemicsensitizationwiththeproteinallergenovalbuminaugmentslocalsensitizationinatopicdermatitis AT parkswc systemicsensitizationwiththeproteinallergenovalbuminaugmentslocalsensitizationinatopicdermatitis |
_version_ |
1718403753235709952 |