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The Effects of Airway Microbiome on Corticosteroid Responsiveness in Asthma AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE Nov 15, 2013 R2. 최하나
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INTRODUCTION Current guidelines recommend the use of corticosteroids to control airway inflammation in persistent asthma. Clinical studies –Up to 45% of patients responding suboptimally to inhaled corticosteroids –Up to 25% of patients do not respond to oral corticosteroids Corticosteroid-resistant (CR) patients –Airway inflammation and remodeling –Severe asthma phenotype –Alternative treatment strategies are needed to improve asthma control
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16S rRNA gene sequence analyses of airway specimens → diversified microbial communities in the airways of subjects with asthma Compared with healthy patients –Asthma patients : significantly higher bacterial burden and diversity caused by expansion of pathogenic bacteria. Moreover, airway microbiome composition and diversity correlate with bronchial hyperresponsiveness. CR asthma : pathogenic microbial communities residing in the airways →inhibit cellular responses to corticosteroids
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METHODS Study Subjects prednisone 20mg bid for 7days CR : FEV1 15% baseline FEV1 < 85%
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Specimen Collection :BAL BAL Differential Analysis Bacterial DNA Extraction, Quantitative PCR, and Sequencing Bacterial Cultures Cell Cultures
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RESULTS Clinical Characteristics Macrophages are the major cell type in the airway lumen, and produce an array of proinflammatory mediators that control responses of various cell types, including T cells and airway epithelium that are involved in host defense, airway inflammation, tissue remodeling, and repair.
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Airway Microbiome in Subjects with Asthma
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Subjects with CR asthma with microbial expansions (24 of 29 patients) Subjects with CS asthma with bacterial expansions (9 of 10 patients)
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Unique Bacterial Genus Expansions in the Airways of CR and CS Subjects with Asthma
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Effects of Bacteria from the Airways on Cell Activation and Response to Corticosteroids in Airway Macrophages
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2uM 10uM
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DISCUSSION
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CONCLUSION A subset of subjects with CR asthma demonstrates airway expansion of specific gram-negative bacteria, which trigger TAK1/MAPK activation and induce corticosteroid resistance. TAK1 inhibition restored cellular sensitivity to corticosteroids.
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