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IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis

BACKGROUND: In asthma interleukin (IL)-13 is increased in the airway compared with non-asthmatic eosinophilic bronchitis. Whether this differential expression is specific to the airway or is more generalised is uncertain. METHODS: We sought to examine IL-13 expression in peripheral blood T-cells and...

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Autores principales: Siddiqui, Salman, Cruse, Glenn, Mckenna, Susan, Monteiro, William, Mistry, Vijay, Wardlaw, Andrew, Brightling, Christopher
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716303/
https://www.ncbi.nlm.nih.gov/pubmed/19602238
http://dx.doi.org/10.1186/1471-2466-9-34
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author Siddiqui, Salman
Cruse, Glenn
Mckenna, Susan
Monteiro, William
Mistry, Vijay
Wardlaw, Andrew
Brightling, Christopher
author_facet Siddiqui, Salman
Cruse, Glenn
Mckenna, Susan
Monteiro, William
Mistry, Vijay
Wardlaw, Andrew
Brightling, Christopher
author_sort Siddiqui, Salman
collection PubMed
description BACKGROUND: In asthma interleukin (IL)-13 is increased in the airway compared with non-asthmatic eosinophilic bronchitis. Whether this differential expression is specific to the airway or is more generalised is uncertain. METHODS: We sought to examine IL-13 expression in peripheral blood T-cells and eosinophils in asthma and non-asthmatic eosinophilic bronchitis. Peripheral blood CD3+ cell and eosinophil intracellular IL-13 expression from subjects with asthma, non-asthmatic eosinophilic bronchitis and healthy controls was assessed. The effect of priming by asthmatic serum on the release of IL-13 by peripheral blood mononuclear cells from healthy subjects was examined and the serum from these subjects was analysed for a range of chemokines and cytokines. RESULTS: The median (IQR)% intracellular IL-13 expression by CD3+ cells was increased in asthma [5.3 (2.7–9.8)%; n = 12] compared to non-asthmatic eosinophilic bronchitis [1.1 (0.5–3)%; n = 7] and healthy controls [1.7 (0.2–3%); n = 9] (p = 0.02), but was not significantly different in eosinophils across the groups. IL-13 released from healthy peripheral blood mononuclear cells (n = 10) was increased by asthmatic serum [117 (47.8–198)pg/ml] compared to control [78.5 (42.6–128)pg/ml; p = 0.02), but was not affected by non-asthmatic serum. CONCLUSION: Our findings support the view that IL-13 expression is increased in peripheral blood-derived T cells in asthma and that asthmatic serum up-regulates IL-13 release from healthy peripheral blood mononuclear cells.
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spelling pubmed-27163032009-07-28 IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis Siddiqui, Salman Cruse, Glenn Mckenna, Susan Monteiro, William Mistry, Vijay Wardlaw, Andrew Brightling, Christopher BMC Pulm Med Research Article BACKGROUND: In asthma interleukin (IL)-13 is increased in the airway compared with non-asthmatic eosinophilic bronchitis. Whether this differential expression is specific to the airway or is more generalised is uncertain. METHODS: We sought to examine IL-13 expression in peripheral blood T-cells and eosinophils in asthma and non-asthmatic eosinophilic bronchitis. Peripheral blood CD3+ cell and eosinophil intracellular IL-13 expression from subjects with asthma, non-asthmatic eosinophilic bronchitis and healthy controls was assessed. The effect of priming by asthmatic serum on the release of IL-13 by peripheral blood mononuclear cells from healthy subjects was examined and the serum from these subjects was analysed for a range of chemokines and cytokines. RESULTS: The median (IQR)% intracellular IL-13 expression by CD3+ cells was increased in asthma [5.3 (2.7–9.8)%; n = 12] compared to non-asthmatic eosinophilic bronchitis [1.1 (0.5–3)%; n = 7] and healthy controls [1.7 (0.2–3%); n = 9] (p = 0.02), but was not significantly different in eosinophils across the groups. IL-13 released from healthy peripheral blood mononuclear cells (n = 10) was increased by asthmatic serum [117 (47.8–198)pg/ml] compared to control [78.5 (42.6–128)pg/ml; p = 0.02), but was not affected by non-asthmatic serum. CONCLUSION: Our findings support the view that IL-13 expression is increased in peripheral blood-derived T cells in asthma and that asthmatic serum up-regulates IL-13 release from healthy peripheral blood mononuclear cells. BioMed Central 2009-07-14 /pmc/articles/PMC2716303/ /pubmed/19602238 http://dx.doi.org/10.1186/1471-2466-9-34 Text en Copyright © 2009 Siddiqui 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
Siddiqui, Salman
Cruse, Glenn
Mckenna, Susan
Monteiro, William
Mistry, Vijay
Wardlaw, Andrew
Brightling, Christopher
IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title_full IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title_fullStr IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title_full_unstemmed IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title_short IL-13 expression by blood T cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
title_sort il-13 expression by blood t cells and not eosinophils is increased in asthma compared to non-asthmatic eosinophilic bronchitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716303/
https://www.ncbi.nlm.nih.gov/pubmed/19602238
http://dx.doi.org/10.1186/1471-2466-9-34
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