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| ID | Type | Description | Link |
|---|---|---|---|
| 2022-A00651- 42 | Registry Identifier | IDRCB |
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Asthma is a common chronic bronchial disease affecting 300 million people worldwide. The disease can be severe when it is not managed properly or when it is not controlled by treatments. Asthma is characterized by bronchial inflammation, bronchial hyperreactivity and tissue remodeling. Symptoms include episodes of coughing, dyspnoea and wheezing in relation with bronchial obstruction. The evolution is marked by the occurrence of exacerbations (increase of symptoms), most often triggered by viral infections, mostly due to rhinoviruses. The treatment of asthma is based on inhaled corticosteroid therapy sometimes combined with other treatments that help control the majority of asthma. However, about 10% of patients suffer from persistent symptoms despite these treatments.
Natural killer (NK) cells are important actors of the antiviral innate immune response and are present in high numbers in the lungs. However, their role in severe asthma and its virus-induced exacerbations is unknown.
The purpose of this work is to characterize NK cells in severe asthma in order to identify molecules expressed differently from control subjects. The goal is to assess whether these molecules could be potential biomarkers of a severe asthma subtype, also known as the endotype, and/or be the molecular control for exacerbation. The advantage of identifying biomarkers for inflammatory diseases lies in their usefulness in establishing a correct diagnosis, monitoring the progress of the disease and the effectiveness of treatments. The secondary objectives are to characterize the activation of NK cells in response to in vitro rhinovirus infection of different types, in monoculture or in a model of interaction with a bronchial epithelium, and identify one or more molecules involved in the interaction between bronchial epithelial cells and NK cells.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Severe uncontrolled asthma in exacerbation | Other |
| |
| Severe uncontrolled asthma excluding exacerbation | Other |
| |
| Severe controlled asthma | Other |
| |
| Healthy volunteers (control group) | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| blood sample | Biological | Blood sample (56mL) taken in a heparin tube |
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in expression of one or more molecules on the surface of NK cells | Rationale for choice of primary endpoint: Our aim is to phenotype NK cells in different groups of severe asthma patients compared with control subjects, in order to identify at least one marker of disease discrimination on these cells. We are therefore looking for previously unknown changes in the expression of one or more molecules. | day 1 to day 2555 |
| Measure | Description | Time Frame |
|---|---|---|
| Measurement of NK cell activation | Change From Baseline in the expression of CD107, CD69 and interferon-É£. | day 1 to day 2555 |
| Measurement of NK cell-induced epithelial cell activation and viability |
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Inclusion Criteria:
Cases asthma controlled, uncontrolled excluding exacerbation, uncontrolled asthma exacerbation, and healthy volunteers:
Cases asthma controlled, uncontrolled excluding exacerbation, uncontrolled exacerbation:
- Diagnosis of severe asthma confirmed by a respirologist at an expert centre
Case asthma controlled:
- Asthma control confirmed by a lung specialist from an expert centre
Case uncontrolled asthma excluding exacerbation:
- Uncontrolled asthma confirmed by a lung specialist from an expert centre
Case uncontrolled asthma with exacerbation:
- Current exacerbation
Exclusion Criteria:
Cases asthma controlled, uncontrolled excluding exacerbation, uncontrolled asthma exacerbation, and healthy volunteers:
Case patient with asthma:
- Coexistence of a chronic inflammatory disease other than asthma
Case healthy volunteers:
- Coexistence of an inflammatory pathology
Exclusion criteria:
Cases asthma: Pregnancy during follow-up Cases healthy volunteers: Total IgE level greater than 100 kU/L (measured on the study sample)
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Pascal Chanez, PU-PH | Contact | +334.91.96.58.64 | pascal.chanez@univ-amu.fr | |
| Catherine Duez, CRCN | Contact | +334.91.32.42.74 | catherine.duez@inserm.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital NORD - AP-HM, Clinique des bronches, de l'allergie et du sommeil | Recruiting | Marseille | 13915 | France |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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Change From Baseline in epithelial cell cohesion, mucin and cytokine (IL-8, type I interferon, IL-33 and TSLP) production
| day 1 to day 2555 |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |