Double-stranded RNA induces disproportionate expression of thymic stromal lymphopoietin versus interferon-beta in bronchial epithelial cells from donors with asthma
Double-stranded RNA induces disproportionate expression of thymic stromal lymphopoietin versus interferon-beta in bronchial epithelial cells from donors with asthma
Background Thymic stromal lymphopoietin (TSLP) is an epithelial cell-derived cytokine that strongly activates dendritic cells and can initiate allergic inflammation. Since exposure to rhinovirus or double-stranded (ds) RNA (a surrogate of viral infection) induces TSLP expression in bronchial epithelial cells (BECs), this cytokine may link innate antiviral responses and the type 2 adaptive immune response.
Objective As BECs from donors with asthma have a deficient interferon (IFN) response to rhinovirus infection, a study was undertaken to test the hypothesis that their antiviral response shows a bias towards TSLP production.
Methods Primary BECs were grown from subjects with asthma and healthy volunteers. After exposure to dsRNA, interleukin (IL)-8, IFN? and TSLP mRNA and protein expression were measured by RT-qPCR and ELISA, respectively.
Results dsRNA dose-dependently increased IL-8 expression in BECs with no significant difference between the groups. However, BECs from subjects with asthma expressed less IFN? and more TSLP mRNA and protein in response to dsRNA than BECs from those without asthma (median (IQR) 57 (38–82) pg/ml vs 106 (57–214) pg/ml for IFN? (p<0.05) and 114 (86–143) pg/ml vs 65 (32–119) pg/ml for TSLP (p<0.05) in response to 10 ?g/ml dsRNA for 24 h). Induction of TSLP mRNA by dsRNA was blocked by Toll-like receptor 3 or protein kinase inhibitors or by preventing de novo protein synthesis, but not by neutralisation of type I IFN receptors.
Conclusion BECs from subjects with asthma are biased towards higher TSLP and lower IFN? production in response to dsRNA, suggesting that viral infection in asthma may lead to an altered mediator profile that biases towards a Th2 immune response.
626-632
Uller, L
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Leino, M.
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Bedke, Nicole
981dbd61-1912-4231-b6d5-42520c38178d
Sammut, David
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Green, B.
b8e56ad0-cfdc-4f53-86d5-d7563d2d6bd1
Lau, L.
2af8045d-6162-4939-aba7-28dd2f60f6a8
Howarth, P.H.
ff19c8c4-86b0-4a88-8f76-b3d87f142a21
Holgate, S.T.
2e7c17a9-6796-436e-8772-1fe6d2ac5edc
Davies, D.E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
July 2010
Uller, L
8f844d19-934a-445d-926c-327d0b140b23
Leino, M.
b9881d87-089f-467a-a0c3-354c03f861d3
Bedke, Nicole
981dbd61-1912-4231-b6d5-42520c38178d
Sammut, David
0c7ac14b-6c2e-4d45-85a0-327703d1afd0
Green, B.
b8e56ad0-cfdc-4f53-86d5-d7563d2d6bd1
Lau, L.
2af8045d-6162-4939-aba7-28dd2f60f6a8
Howarth, P.H.
ff19c8c4-86b0-4a88-8f76-b3d87f142a21
Holgate, S.T.
2e7c17a9-6796-436e-8772-1fe6d2ac5edc
Davies, D.E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
Uller, L, Leino, M., Bedke, Nicole, Sammut, David, Green, B., Lau, L., Howarth, P.H., Holgate, S.T. and Davies, D.E.
(2010)
Double-stranded RNA induces disproportionate expression of thymic stromal lymphopoietin versus interferon-beta in bronchial epithelial cells from donors with asthma.
Thorax, 65 (7), .
(doi:10.1136/thx.2009.125930).
Abstract
Background Thymic stromal lymphopoietin (TSLP) is an epithelial cell-derived cytokine that strongly activates dendritic cells and can initiate allergic inflammation. Since exposure to rhinovirus or double-stranded (ds) RNA (a surrogate of viral infection) induces TSLP expression in bronchial epithelial cells (BECs), this cytokine may link innate antiviral responses and the type 2 adaptive immune response.
Objective As BECs from donors with asthma have a deficient interferon (IFN) response to rhinovirus infection, a study was undertaken to test the hypothesis that their antiviral response shows a bias towards TSLP production.
Methods Primary BECs were grown from subjects with asthma and healthy volunteers. After exposure to dsRNA, interleukin (IL)-8, IFN? and TSLP mRNA and protein expression were measured by RT-qPCR and ELISA, respectively.
Results dsRNA dose-dependently increased IL-8 expression in BECs with no significant difference between the groups. However, BECs from subjects with asthma expressed less IFN? and more TSLP mRNA and protein in response to dsRNA than BECs from those without asthma (median (IQR) 57 (38–82) pg/ml vs 106 (57–214) pg/ml for IFN? (p<0.05) and 114 (86–143) pg/ml vs 65 (32–119) pg/ml for TSLP (p<0.05) in response to 10 ?g/ml dsRNA for 24 h). Induction of TSLP mRNA by dsRNA was blocked by Toll-like receptor 3 or protein kinase inhibitors or by preventing de novo protein synthesis, but not by neutralisation of type I IFN receptors.
Conclusion BECs from subjects with asthma are biased towards higher TSLP and lower IFN? production in response to dsRNA, suggesting that viral infection in asthma may lead to an altered mediator profile that biases towards a Th2 immune response.
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Published date: July 2010
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Local EPrints ID: 186109
URI: http://eprints.soton.ac.uk/id/eprint/186109
ISSN: 0040-6376
PURE UUID: 14c813ae-b14b-4c47-8428-8f2b1368d647
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Date deposited: 12 May 2011 10:45
Last modified: 15 Mar 2024 02:35
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Author:
L Uller
Author:
M. Leino
Author:
Nicole Bedke
Author:
David Sammut
Author:
B. Green
Author:
L. Lau
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