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The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex

BACKGROUND: The relationships between total serum IgE levels and gene expression patterns in peripheral blood CD4+ T cells (in all subjects and within each sex specifically) are not known. METHODS: Peripheral blood CD4+ T cells from 223 participants from the Childhood Asthma Management Program (CAMP...

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Autores principales: Hunninghake, Gary M, Chu, Jen-hwa, Sharma, Sunita S, Cho, Michael H, Himes, Blanca E, Rogers, Angela J, Murphy, Amy, Carey, Vincent J, Raby, Benjamin A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080837/
https://www.ncbi.nlm.nih.gov/pubmed/21473777
http://dx.doi.org/10.1186/1471-2466-11-17
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author Hunninghake, Gary M
Chu, Jen-hwa
Sharma, Sunita S
Cho, Michael H
Himes, Blanca E
Rogers, Angela J
Murphy, Amy
Carey, Vincent J
Raby, Benjamin A
author_facet Hunninghake, Gary M
Chu, Jen-hwa
Sharma, Sunita S
Cho, Michael H
Himes, Blanca E
Rogers, Angela J
Murphy, Amy
Carey, Vincent J
Raby, Benjamin A
author_sort Hunninghake, Gary M
collection PubMed
description BACKGROUND: The relationships between total serum IgE levels and gene expression patterns in peripheral blood CD4+ T cells (in all subjects and within each sex specifically) are not known. METHODS: Peripheral blood CD4+ T cells from 223 participants from the Childhood Asthma Management Program (CAMP) with simultaneous measurement of IgE. Total RNA was isolated, and expression profiles were generated with Illumina HumanRef8 v2 BeadChip arrays. Modeling of the relationship between genome-wide gene transcript levels and IgE levels was performed in all subjects, and stratified by sex. RESULTS: Among all subjects, significant evidence for association between gene transcript abundance and IgE was identified for a single gene, the interleukin 17 receptor B (IL17RB), explaining 12% of the variance (r(2)) in IgE measurement (p value = 7 × 10(-7), 9 × 10(-3 )after adjustment for multiple testing). Sex stratified analyses revealed that the correlation between IL17RB and IgE was restricted to males only (r(2 )= 0.19, p value = 8 × 10(-8); test for sex-interaction p < 0.05). Significant correlation between gene transcript abundance and IgE level was not found in females. Additionally we demonstrated substantial sex-specific differences in IgE when considering multi-gene models, and in canonical pathway analyses of IgE level. CONCLUSIONS: Our results indicate that IL17RB may be the only gene expressed in CD4+ T cells whose transcript measurement is correlated with the variation in IgE level in asthmatics. These results provide further evidence sex may play a role in the genomic regulation of IgE.
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spelling pubmed-30808372011-04-22 The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex Hunninghake, Gary M Chu, Jen-hwa Sharma, Sunita S Cho, Michael H Himes, Blanca E Rogers, Angela J Murphy, Amy Carey, Vincent J Raby, Benjamin A BMC Pulm Med Research Article BACKGROUND: The relationships between total serum IgE levels and gene expression patterns in peripheral blood CD4+ T cells (in all subjects and within each sex specifically) are not known. METHODS: Peripheral blood CD4+ T cells from 223 participants from the Childhood Asthma Management Program (CAMP) with simultaneous measurement of IgE. Total RNA was isolated, and expression profiles were generated with Illumina HumanRef8 v2 BeadChip arrays. Modeling of the relationship between genome-wide gene transcript levels and IgE levels was performed in all subjects, and stratified by sex. RESULTS: Among all subjects, significant evidence for association between gene transcript abundance and IgE was identified for a single gene, the interleukin 17 receptor B (IL17RB), explaining 12% of the variance (r(2)) in IgE measurement (p value = 7 × 10(-7), 9 × 10(-3 )after adjustment for multiple testing). Sex stratified analyses revealed that the correlation between IL17RB and IgE was restricted to males only (r(2 )= 0.19, p value = 8 × 10(-8); test for sex-interaction p < 0.05). Significant correlation between gene transcript abundance and IgE level was not found in females. Additionally we demonstrated substantial sex-specific differences in IgE when considering multi-gene models, and in canonical pathway analyses of IgE level. CONCLUSIONS: Our results indicate that IL17RB may be the only gene expressed in CD4+ T cells whose transcript measurement is correlated with the variation in IgE level in asthmatics. These results provide further evidence sex may play a role in the genomic regulation of IgE. BioMed Central 2011-04-07 /pmc/articles/PMC3080837/ /pubmed/21473777 http://dx.doi.org/10.1186/1471-2466-11-17 Text en Copyright ©2011 Hunninghake et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hunninghake, Gary M
Chu, Jen-hwa
Sharma, Sunita S
Cho, Michael H
Himes, Blanca E
Rogers, Angela J
Murphy, Amy
Carey, Vincent J
Raby, Benjamin A
The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title_full The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title_fullStr The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title_full_unstemmed The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title_short The CD4+ T-cell transcriptome and serum IgE in asthma: IL17RB and the role of sex
title_sort cd4+ t-cell transcriptome and serum ige in asthma: il17rb and the role of sex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080837/
https://www.ncbi.nlm.nih.gov/pubmed/21473777
http://dx.doi.org/10.1186/1471-2466-11-17
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