NKAS: NK Cells in Severe Asthma

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06015256
Collaborator
(none)
448
1
4
84
5.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Biological: blood sample
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
448 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Characterization of Natural Killer Cells in Severe Asthma Patients in Comparison With Control Subjects: Identification of Biomarkers, Response During Virus-induced Exacerbations, and Interaction With Bronchial Epithelial Cells
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2028
Anticipated Study Completion Date :
Sep 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Other: Severe uncontrolled asthma in exacerbation

Biological: blood sample
Blood sample (56mL) taken in a heparin tube

Other: Severe uncontrolled asthma excluding exacerbation

Biological: blood sample
Blood sample (56mL) taken in a heparin tube

Other: Severe controlled asthma

Biological: blood sample
Blood sample (56mL) taken in a heparin tube

Other: Healthy volunteers (control group)

Biological: blood sample
Blood sample (56mL) taken in a heparin tube

Outcome Measures

Primary Outcome Measures

  1. Changes in expression of one or more molecules on the surface of NK cells [day 1 to day 2555]

    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.

Secondary Outcome Measures

  1. Measurement of NK cell activation [day 1 to day 2555]

    Change From Baseline in the expression of CD107, CD69 and interferon-ɣ.

  2. Measurement of NK cell-induced epithelial cell activation and viability [day 1 to day 2555]

    Change From Baseline in epithelial cell cohesion, mucin and cytokine (IL-8, type I interferon, IL-33 and TSLP) production

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Cases asthma controlled, uncontrolled excluding exacerbation, uncontrolled asthma exacerbation, and healthy volunteers:

  • Consent form read, understood, approved and signed before any study procedure

  • Membership of a social security scheme or beneficiary of such a scheme

  • Patient aged over 18

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:

  • Person subject to a legal protection measure

  • Vulnerable population: minors, persons under guardianship or trusteeship or persons deprived of their rights to liberty by court order.

  • women with a known pregnancy

  • Inability or refusal to comply with research requirements

  • Active or weaned smoker > 15 PA

  • Treatment with non-steroidal anti-inflammatory drugs (NSAIDs) or opioids in the 10 days prior to inclusion

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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital NORD - AP-HM, Clinique des bronches, de l'allergie et du sommeil Marseille France 13915

Sponsors and Collaborators

  • Institut National de la Santé Et de la Recherche Médicale, France

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut National de la Santé Et de la Recherche Médicale, France
ClinicalTrials.gov Identifier:
NCT06015256
Other Study ID Numbers:
  • C21-75
  • 2022-A00651- 42
First Posted:
Aug 29, 2023
Last Update Posted:
Aug 29, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 29, 2023