The University of Southampton
University of Southampton Institutional Repository

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
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.
0040-6376
626-632
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
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), 626-632. (doi:10.1136/thx.2009.125930).

Record type: Article

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.

This record has no associated files available for download.

More information

Published date: July 2010

Identifiers

Local EPrints ID: 186109
URI: http://eprints.soton.ac.uk/id/eprint/186109
ISSN: 0040-6376
PURE UUID: 14c813ae-b14b-4c47-8428-8f2b1368d647
ORCID for D.E. Davies: ORCID iD orcid.org/0000-0002-5117-2991

Catalogue record

Date deposited: 12 May 2011 10:45
Last modified: 15 Mar 2024 02:35

Export record

Altmetrics

Contributors

Author: L Uller
Author: M. Leino
Author: Nicole Bedke
Author: David Sammut
Author: B. Green
Author: L. Lau
Author: P.H. Howarth
Author: S.T. Holgate
Author: D.E. Davies ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×