IL-SAA: IL-13 Blockade and Airway Autoimmunity in Asthma
Study Details
Study Description
Brief Summary
It has been observed that certain section of patients having severe to moderate Asthma, do not benefit from oral corticosteroids and IL-5 blocking biologics. There is increasing evidence that Airway auto immunity may be responsible for this poor response to treatment. It has been seen in earlier study done at Nair lab that these patients might benefit from Dupilumab, a biologic blocking IL-13/ IL-4. IL-13/IL-4 are the cytokines responsible for increased inflammation in these Asthmatics. The hypothesis is that blocking IL-13/IL-4 will also reduce the airway auto immunity which can be measured by comparing the auto immune markers in airway at baseline (before starting Dupilumab) and 16 weeks (after 4 months of Dupilumab treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Asthma, a chronic airway disease characterized by reversible airflow, airway inflammation and hyper responsiveness. A prominent phenotype is eosinophilic asthma, with a prevalence rate of ~50% and characterised by blood eosinophils >300 cells/μL and sputum eosinophils >3%. Inhaled corticosteroids (ICS) have been successful for treatment of mild-to-moderate asthma. However, ~10% of eosinophilic asthmatics remain uncontrolled despite being on high dose oral corticosteroids. This small percentage contributes disproportionately to 80% of asthma healthcare costs [8-10]. As a steroid-sparing strategy, monoclonal antibody (mAb) therapies targeting interleukin (IL)-5 signalling have been developed that are projected to benefit this difficult-to-treat population. Yet, a subset (30-50%) of them remain symptomatic despite being on oral corticosteroids (OCS) and adjunct anti-IL-5 mAb. Anti- eosinophil peroxidase (EPX) Immunoglobulin G (IgG) levels in the airways strongly correlated with the presence of other auto antibodies, in particular the anti-nuclear antibodies (ANAs) as well as various clinical features of asthma severity. Therefore, a better understanding of the underlying pathology with subsequent identification of clinical/molecular biomarkers remains an unmet clinical need for optimal asthma management. Airway autoimmune responses in severe asthma is an important contributor to airway mucus and this can be ameliorated by blocking the IL-4/IL-13 inflammatory axis.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Subjects with Eosinophilic Asthma
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| Subjects without Asthma
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Outcome Measures
Primary Outcome Measures
- The proportion of severe asthmatics with a reduction in anti-EPX IgG in airway secretions (marker of airway autoimmunity) [12 weeks]
Eligibility Criteria
Criteria
Inclusion Criteria:
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- Prior to the beginning of the study, patients must be willing and fully capable to provide written informed consent 2. Subjects must be able and willing to comply with the study protocol 3. Asthma diagnosed by a respiratory physician ≥ 36 months prior to study enrollment based on the Global Initiative for Asthma (GINA) 2014 guidelines 4. Patients referred or routinely followed for asthma by Dr. Nair 5. Clinical indication to prescribe dupilumab or will enter a clinical trial where patient will receive drug for at least 4 months 6. ICS dose ≥ 500 mcg of fluticasone equivalent/day, and/or daily prednisone 7. • Asthma control questionnaire (ACQ) ≥ 1.5 at Visit 1 8. Bronchodilator reversibility at Visit 1, indicated by an improvement in forced expiratory volume at one second (FEV1) ≥ 12% and 200 milli Litre
Exclusion Criteria:
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- Current smoker defined as having smoked at least one cigarette (or pipe, cigar, or marijuana) per day for ≥ 30 days within the three months prior to screening 2. Ex-smokers with ≥ 20 pack-year smoking history 3. Current pregnancy or lactation 4. Treatment with anti- Immunoglobulin E (IgE), anti-IL-5, or anti-IL-5 Receptor targeted therapy currently or within three months prior to Visit 1 5. Any prior medical conditions or treatment history that the physician deems unfit (including but not restricted to chronic obstructive pulmonary disease, idiopathic pulmonary fibrosis, cystic fibrosis, pulmonary arterial hypertension, tuberculosis).
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- McMaster University
- Sanofi
Investigators
- Principal Investigator: Manali Mukherjee, PHD, McMaster University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 14816