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Effects of corticosteroid on the expression of thymus and activation-regulated chemokine in a murine model of allergic asthma.

Authors: Kurokawa, M  Kokubu, F  Matsukura, S  Kawaguchi, M  Ieki, K  Suzuki, S  Odaka, M  Watanabe, S  Takeuchi, H  Akabane, T  Asano, K  Iwase, M  Honma, I  Adachi, M 
Citation: Kurokawa M, etal., Int Arch Allergy Immunol. 2005;137 Suppl 1:60-8. Epub 2005 Jun 2.
Pubmed: (View Article at PubMed) PMID:15947487
DOI: Full-text: DOI:10.1159/000085434

BACKGROUND: Thymus and activation-regulated chemokine (TARC; CCL17) is a lymphocyte-directed CC chemokine that specifically attracts T-helper (Th) 2 cells positive for the CC chemokine receptor 4 (CCR4(+)). Corticosteroids reduce airway inflammation, as reflected by reduced numbers of eosinophils and T cells and reduced expression of cytokines. We investigated TARC production and the inhibitory effects of corticosteroids on TARC expression in a murine model of allergic asthma. METHODS: BALB/c mice were sensitized by intraperitoneal injection of ovalbumin (OVA) with alum. Once daily for 1 week, mice received injections of dexamethasone or 0.2 ml saline (control), then 1 h later inhaled aerosolized 1% OVA for 30 min. Mice were killed 24 h after OVA challenge for bronchoalveolar lavage and lung tissue examination. RESULTS: TARC was expressed mainly in the bronchial epithelial cells. Dexamethasone attenuated OVA-induced airway eosinophilia, lymphocyte infiltration, and airway hyperresponsiveness. Dexamethasone also decreased TARC production in the bronchoalveolar lavage fluid and decreased expression of TARC mRNA and TARC protein in lung tissue. CONCLUSIONS: The corticosteroid dexamethasone inhibits TARC production in a murine model of allergic asthma in vivo. The beneficial effect of corticosteroids in bronchial asthma is due in part to their direct inhibitory effects on TARC production.


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CRRD Object Information
CRRD ID: 4145513
Created: 2010-11-08
Species: All species
Last Modified: 2010-11-08
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.