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Janus kinase 1/3 signaling pathways are key initiators of TH2 differentiation and lung allergic responses.
Janus kinase 1/3 signaling pathways are key initiators of TH2 differentiation and lung allergic responses.
- Source :
-
The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2014 Apr; Vol. 133 (4), pp. 1162-74. Date of Electronic Publication: 2013 Dec 22. - Publication Year :
- 2014
-
Abstract
- Background: Janus kinases (JAKs) are regulators of signaling through cytokine receptors. The importance of JAK1/3 signaling on TH2 differentiation and development of lung allergic responses has not been investigated.<br />Objective: We sought to examine a selective JAK1/3 inhibitor (R256) on differentiation of TH subsets in vitro and on development of ovalbumin (OVA)-induced airway hyperresponsiveness (AHR) and inflammation in an experimental model of asthma.<br />Methods: A selective JAK1/3 inhibitor was used to assay the importance of this pathway on induction of TH1, TH2, and TH17 differentiation in vitro. In vivo, the effects of inhibiting JAK1/3 signaling were examined by administering the inhibitor during the sensitization or allergen challenge phases in the primary challenge model or just before provocative challenge in the secondary challenge model. Airway inflammation and AHR were examined after the last airway challenge.<br />Results: In vitro, R256 inhibited differentiation of TH2 but not TH1 or TH17 cells, which was associated with downregulation of signal transducer and activator of transcription (STAT) 6 and STAT5 phosphorylation. However, once polarized, TH2 cells were unaffected by the inhibitor. In vivo, R256 administered during the OVA sensitization phase prevented the development of AHR, airway eosinophilia, mucus hypersecretion, and TH2 cytokine production without changes in TH1 and TH17 cytokine levels, indicating that selective blockade of TH2 differentiation was critical. Inhibitor administration after OVA sensitization but during the challenge phases in the primary or secondary challenge models similarly suppressed AHR, airway eosinophilia, and mucus hypersecretion without any reduction in TH2 cytokine production, suggesting the inhibitory effects were downstream of TH2 cytokine receptor signaling pathways.<br />Conclusions: Targeting the TH2-dependent JAK/STAT activation pathway represents a novel therapeutic approach for the treatment of asthma.<br /> (Copyright © 2013 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.)
- Subjects :
- Allergens administration & dosage
Allergens immunology
Animals
Disease Models, Animal
Female
Janus Kinase 1 antagonists & inhibitors
Janus Kinase 3 antagonists & inhibitors
Lung immunology
Lung metabolism
Lung pathology
Mice
Mice, Transgenic
Protein Kinase Inhibitors pharmacology
Respiratory Hypersensitivity pathology
T-Lymphocytes, Helper-Inducer cytology
T-Lymphocytes, Helper-Inducer drug effects
T-Lymphocytes, Helper-Inducer immunology
T-Lymphocytes, Helper-Inducer metabolism
Th2 Cells drug effects
Th2 Cells immunology
Cell Differentiation
Janus Kinase 1 metabolism
Janus Kinase 3 metabolism
Respiratory Hypersensitivity immunology
Respiratory Hypersensitivity metabolism
Signal Transduction drug effects
Th2 Cells cytology
Th2 Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-6825
- Volume :
- 133
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The Journal of allergy and clinical immunology
- Publication Type :
- Academic Journal
- Accession number :
- 24365136
- Full Text :
- https://doi.org/10.1016/j.jaci.2013.10.036