Immune Airway-Epithelial Interactions in Steroid-Refractory Severe Asthma
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Asthma
- Sponsor
- University of Pittsburgh
- Enrollment
- 115
- Locations
- 1
- Primary Endpoint
- Eotaxin-3 and IL-27 expression and their downstream signatures
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
This research study is being done to learn more about severe asthma by comparing people with severe asthma to those with milder forms of asthma and people without asthma, at baseline and over time. Individuals are being asked to join a research study to help understand the differences in the lungs and blood of participants with severe asthma compared to those with milder asthma and healthy individuals, as well as differences in overall health. Investigators also want to determine whether these differences predict asthma-related and biologic outcomes over 1 year of follow up.
Detailed Description
This study will obtain human lung samples by bronchoscopy from a range of asthmatics and healthy controls to address questions related to the mechanisms for the development of the complex immune processes observed in the lungs. Samples will be evaluated for Type-1, Type-2 and Interleukin-27 (IL-27) expression (and their downstream signatures). In addition, these samples will be evaluated for the presence or absence of Interleukin-10 (IL-10) as a counter regulatory pathway. These pathways will be directly evaluated in epithelial brushings and bronchoalveolar lavage (BAL) cells, as well as BAL fluid. Broad gene expression profiling (Ribonucleic acid (RNA)-sequencing) will also be performed to determine the range of immune-inflammatory markers present in these severe asthmatics. Investigators will specifically address the Signal Transducers and Activators of Transcription (STAT) signaling pathways, particularly STAT-1 and STAT-3 to determine the pattern of activation and downstream responses to develop new therapies. Additionally, in a subset, investigators will compare targeted and untargeted gene expression as obtained from bronchoscopic samples with expression obtained from clinically performed video assisted thoracoscopic (VATS) biopsies of very severe systemic corticosteroid dependent patients. The ultimate goal of this studies is to determine whether a predictive biomarker panel can be identified in the less invasive bronchoscopic samples which predict the findings seen on VATS biopsy.
Investigators
Sally E. Wenzel MD
MD
University of Pittsburgh
Eligibility Criteria
Inclusion Criteria
- •18-65 years of age
- •Non-smoker
- •Asthmatic subjects must also demonstrate forced expiratory volume in 1 second (FEV1) bronchodilator reversibility ≥12% or airway hyperresponsiveness reflected by a methacholine provocative concentration causing a 20% fall in FEV1 (PC20) ≤16 mg/mL (Historical methacholine data from previous National Institutes of Health (NIH) trial will be allowed)
Exclusion Criteria
- •Greater than 10 pack year smoking history (none in the last year)
- •Vocal cord dysfunction, cystic fibrosis or chronic obstructive pulmonary disorder
- •Other lung disease, or any coronary artery disease, hypertension, diabetes or renal failure that is not well-controlled.
- •Healthy Controls only: Pre-bronchodilator FEV1/Forced vital capacity (FVC) \<0.70 or an improvement in FEV1 of more than 12% following 4 puffs of albuterol.
Outcomes
Primary Outcomes
Eotaxin-3 and IL-27 expression and their downstream signatures
Time Frame: 1 Year
Measure eotaxin-3 and IL-27 expression in bronchoalveolar lavage cells and epithelial cells.
Secondary Outcomes
- Targeted and untargeted gene expression as obtained from bronchoscopic samples(1 Year)
- Global gene expression in the airway epithelium and bronchoalveolar lavage cells using RNA-sequencing(1 Year)
- Signal transducer and activator of transcription (STAT) signaling pathways(1 Year)