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TH2 and TH17 inflammatory pathways are reciprocally regulated in asthma

Lookup NU author(s): Dr Lee Borthwick

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


Abstract

Increasing evidence suggests that asthma is a heterogeneous disorder regulated by distinct molecular mechanisms. In a cross-sectional study of asthmatics of varying severity (n = 51), endobronchial tissue gene expression analysis revealed three major patient clusters: T(H)2-high, T(H)17-high, and T(H)2/17-low. T(H)2-high and T(H)17-high patterns were mutually exclusive in individual patient samples, and their gene signatures were inversely correlated and differentially regulated by interleukin-13 (IL-13) and IL-17A. To understand this dichotomous pattern of T helper 2 (T(H)2) and T(H)17 signatures, we investigated the potential of type 2 cytokine suppression in promoting T(H)17 responses in a preclinical model of allergen-induced asthma. Neutralization of IL-4 and/or IL-13 resulted in increased T(H)17 cells and neutrophilic inflammation in the lung. However, neutralization of IL-13 and IL-17 protected mice from eosinophilia, mucus hyperplasia, and airway hyperreactivity and abolished the neutrophilic inflammation, suggesting that combination therapies targeting both pathways may maximize therapeutic efficacy across a patient population comprising both T(H)2 and T(H)17 endotypes.


Publication metadata

Author(s): Choy DF, Hart KM, Borthwick LA, Shikotra A, Nagarkar DR, Siddiqui S, Jia GQ, Ohri CM, Doran E, Vannella KM, Butler CA, Hargadon B, Sciurba JC, Gieseck RL, Thompson RW, White S, Abbas AR, Jackman J, Wu LC, Egen JG, Heaney LG, Ramalingam TR, Arron JR, Wynn TA, Bradding P

Publication type: Article

Publication status: Published

Journal: Science Translational Medicine

Year: 2015

Volume: 7

Issue: 301

Pages: 1-10

Online publication date: 19/08/2015

Acceptance date: 02/07/2015

Date deposited: 26/05/2016

ISSN (print): 1946-6234

ISSN (electronic): 1946-6242

Publisher: American Association for the Advancement of Science

URL: http://dx.doi.org/10.1126/scitranslmed.aab3142

DOI: 10.1126/scitranslmed.aab3142


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Funding

Funder referenceFunder name
Genentech Inc.
Intramural Research Program of the NIH
National Institute for Health Research (NIHR) Leicester Respiratory Biomedical Research Unit
NIAID
AUK-PG-2013-208Asthma UK

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