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PMID: 12760963 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Resolution of airway inflammation following ovalbumin inhalation: comparison of ISS DNA and corticosteroids.

American journal of respiratory cell and molecular biology ·Vol. 28 ·No. 6 ·2003-06-00 ·Pages 655-63

Ikeda RK, Nayar J, Cho JY, Miller M, Rodriguez M, Raz E, Broide DH

Abstract

In this study we have compared the therapeutic effect of the administration of immunostimulatory DNA sequences (ISS) with that of corticosteroids on the resolution of airway inflammation and airway hyperreactivity (AHR) in a mouse model. Mice which had already developed significant levels of eosinophilic airway inflammation 24 h after allergen challenge were then treated with either ISS or corticosteroids, and the effect on AHR and airway inflammation assessed 6 d later. ISS inhibited AHR as effectively as corticosteroids. Combination therapy with ISS and corticosteroids was more effective than monotherapy with either ISS or corticosteroids in inhibiting AHR. In ovalbumin-challenged mice, levels of bronchoalveolar lavage (BAL) eosinophils were significantly reduced with either ISS or corticosteroids. ISS induced significant levels of BAL interferon-gamma, whereas corticosteroids did not induce expression of BAL interferon-gamma. Both ISS and corticosteroids significantly reduced levels of interleukin-5 in BAL, as well as the number of Periodic Acid Schiff-positive airway epithelial cells. Corticosteroids, but not ISS, increased the number of eosinophils in regional mediastinal lymph nodes. Very few apoptotic peribronchial cells were noted following ovalbumin challenge as assessed by TUNEL assay. Corticosteroids, but not ISS, induced an increase in the small number of apoptotic peribronchial cells. The mechanism by which either ISS or corticosteroids inhibit AHR is likely to be mediated by distinct and shared cellular pathways. The combination of the shared and distinct anti-inflammatory pathways may account for the additive effect of ISS and corticosteroids on inhibiting AHR.

MeSH Terms
Administration, Inhalation Adrenal Cortex Hormones/adverse effects,therapeutic use Animals Anti-Inflammatory Agents/adverse effects,therapeutic use Apoptosis/drug effects Bronchial Hyperreactivity/chemically induced,pathology,prevention & control Bronchoalveolar Lavage Fluid/chemistry,cytology DNA/immunology,therapeutic use Dexamethasone/adverse effects,therapeutic use Disease Models, Animal Drug Therapy, Combination Eosinophils/metabolism,pathology Female Inflammation/chemically induced,drug therapy Injections, Intraperitoneal Interferon-gamma/drug effects,metabolism Interleukin-5/metabolism Lymph Nodes/pathology Lymphocytes/drug effects Mice Mice, Inbred BALB C Ovalbumin/administration & dosage,adverse effects,immunology Pulmonary Eosinophilia/chemically induced,drug therapy,pathology Respiratory Hypersensitivity/chemically induced,drug therapy Treatment Outcome
Chemicals
Adrenal Cortex Hormones Anti-Inflammatory Agents Interleukin-5 Dexamethasone Interferon-gamma Ovalbumin DNA
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ikeda Reid K
Department of Medicine, University of California-San Diego, La Jolla, CA 92093-0635, USA.
Nayar Jyothi
Cho Jae Youn
Miller Marina
Rodriguez Monica
Raz Eyal
Broide David H
Article Info
Journal
American journal of respiratory cell and molecular biology
Abbr.
Am J Respir Cell Mol Biol
ISSN
1044-1549
Published
2003-06-00
Pages
655-63
Language
English
Region
United States
NLM ID
8917225
Subset
IM
Grants
NIAID NIH HHS · AI 33977 · United States
NIAID NIH HHS · AI 38425 · United States
NIAID NIH HHS · AI 40682 · United States
NHLBI NIH HHS · T32 HL07022 · United States
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