Cargando…

Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype

BACKGROUND: Egg allergy is one of the most common food allergies of childhood. There is a lack of information on the immunologic basis of egg allergy beyond the role of IgE. OBJECTIVE: To use transcriptional profiling as a novel approach to uncover immunologic processes associated with different phe...

Descripción completa

Detalles Bibliográficos
Autores principales: Kosoy, Roman, Agashe, Charuta, Grishin, Alexander, Leung, Donald Y., Wood, Robert A., Sicherer, Scott H., Jones, Stacie M., Burks, A. Wesley, Davidson, Wendy F., Lindblad, Robert W., Dawson, Peter, Merad, Miriam, Kidd, Brian A., Dudley, Joel T., Sampson, Hugh A., Berin, M. Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082817/
https://www.ncbi.nlm.nih.gov/pubmed/27788149
http://dx.doi.org/10.1371/journal.pone.0163831
_version_ 1782463128349442048
author Kosoy, Roman
Agashe, Charuta
Grishin, Alexander
Leung, Donald Y.
Wood, Robert A.
Sicherer, Scott H.
Jones, Stacie M.
Burks, A. Wesley
Davidson, Wendy F.
Lindblad, Robert W.
Dawson, Peter
Merad, Miriam
Kidd, Brian A.
Dudley, Joel T.
Sampson, Hugh A.
Berin, M. Cecilia
author_facet Kosoy, Roman
Agashe, Charuta
Grishin, Alexander
Leung, Donald Y.
Wood, Robert A.
Sicherer, Scott H.
Jones, Stacie M.
Burks, A. Wesley
Davidson, Wendy F.
Lindblad, Robert W.
Dawson, Peter
Merad, Miriam
Kidd, Brian A.
Dudley, Joel T.
Sampson, Hugh A.
Berin, M. Cecilia
author_sort Kosoy, Roman
collection PubMed
description BACKGROUND: Egg allergy is one of the most common food allergies of childhood. There is a lack of information on the immunologic basis of egg allergy beyond the role of IgE. OBJECTIVE: To use transcriptional profiling as a novel approach to uncover immunologic processes associated with different phenotypes of egg allergy. METHODS: Peripheral blood mononuclear cells (PBMCs) were obtained from egg-allergic children who were defined as reactive (BER) or tolerant (BET) to baked egg, and from food allergic controls (AC) who were egg non-allergic. PBMCs were stimulated with egg white protein. Gene transcription was measured by microarray after 24 h, and cytokine secretion by multiplex assay after 5 days. RESULTS: The transcriptional response of PBMCs to egg protein differed between BER and BET versus AC subjects. Compared to the AC group, the BER group displayed increased expression of genes associated with allergic inflammation as well as corresponding increased secretion of IL-5, IL-9 and TNF-α. A similar pattern was observed for the BET group. Further similarities in gene expression patterns between BER and BET groups, as well as some important differences, were revealed using a novel Immune Annotation resource developed for this project. This approach identified several novel processes not previously associated with egg allergy, including positive associations with TLR4-stimulated myeloid cells and activated NK cells, and negative associations with an induced Treg signature. Further pathway analysis of differentially expressed genes comparing BER to BET subjects showed significant enrichment of IFN-α and IFN-γ response genes, as well as genes associated with virally-infected DCs. CONCLUSIONS: Transcriptional profiling identified several novel pathways and processes that differed when comparing the response to egg allergen in BET, BER, and AC groups. We conclude that this approach is a useful hypothesis-generating mechanism to identify novel immune processes associated with allergy and tolerance to forms of egg.
format Online
Article
Text
id pubmed-5082817
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-50828172016-11-04 Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype Kosoy, Roman Agashe, Charuta Grishin, Alexander Leung, Donald Y. Wood, Robert A. Sicherer, Scott H. Jones, Stacie M. Burks, A. Wesley Davidson, Wendy F. Lindblad, Robert W. Dawson, Peter Merad, Miriam Kidd, Brian A. Dudley, Joel T. Sampson, Hugh A. Berin, M. Cecilia PLoS One Research Article BACKGROUND: Egg allergy is one of the most common food allergies of childhood. There is a lack of information on the immunologic basis of egg allergy beyond the role of IgE. OBJECTIVE: To use transcriptional profiling as a novel approach to uncover immunologic processes associated with different phenotypes of egg allergy. METHODS: Peripheral blood mononuclear cells (PBMCs) were obtained from egg-allergic children who were defined as reactive (BER) or tolerant (BET) to baked egg, and from food allergic controls (AC) who were egg non-allergic. PBMCs were stimulated with egg white protein. Gene transcription was measured by microarray after 24 h, and cytokine secretion by multiplex assay after 5 days. RESULTS: The transcriptional response of PBMCs to egg protein differed between BER and BET versus AC subjects. Compared to the AC group, the BER group displayed increased expression of genes associated with allergic inflammation as well as corresponding increased secretion of IL-5, IL-9 and TNF-α. A similar pattern was observed for the BET group. Further similarities in gene expression patterns between BER and BET groups, as well as some important differences, were revealed using a novel Immune Annotation resource developed for this project. This approach identified several novel processes not previously associated with egg allergy, including positive associations with TLR4-stimulated myeloid cells and activated NK cells, and negative associations with an induced Treg signature. Further pathway analysis of differentially expressed genes comparing BER to BET subjects showed significant enrichment of IFN-α and IFN-γ response genes, as well as genes associated with virally-infected DCs. CONCLUSIONS: Transcriptional profiling identified several novel pathways and processes that differed when comparing the response to egg allergen in BET, BER, and AC groups. We conclude that this approach is a useful hypothesis-generating mechanism to identify novel immune processes associated with allergy and tolerance to forms of egg. Public Library of Science 2016-10-27 /pmc/articles/PMC5082817/ /pubmed/27788149 http://dx.doi.org/10.1371/journal.pone.0163831 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Kosoy, Roman
Agashe, Charuta
Grishin, Alexander
Leung, Donald Y.
Wood, Robert A.
Sicherer, Scott H.
Jones, Stacie M.
Burks, A. Wesley
Davidson, Wendy F.
Lindblad, Robert W.
Dawson, Peter
Merad, Miriam
Kidd, Brian A.
Dudley, Joel T.
Sampson, Hugh A.
Berin, M. Cecilia
Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title_full Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title_fullStr Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title_full_unstemmed Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title_short Transcriptional Profiling of Egg Allergy and Relationship to Disease Phenotype
title_sort transcriptional profiling of egg allergy and relationship to disease phenotype
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082817/
https://www.ncbi.nlm.nih.gov/pubmed/27788149
http://dx.doi.org/10.1371/journal.pone.0163831
work_keys_str_mv AT kosoyroman transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT agashecharuta transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT grishinalexander transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT leungdonaldy transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT woodroberta transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT sichererscotth transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT jonesstaciem transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT burksawesley transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT davidsonwendyf transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT lindbladrobertw transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT dawsonpeter transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT meradmiriam transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT kiddbriana transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT dudleyjoelt transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT sampsonhugha transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype
AT berinmcecilia transcriptionalprofilingofeggallergyandrelationshiptodiseasephenotype