Characterization of Natural Killer Cells in Severe Asthma Patients in Comparison With Control Subjects (NKAS)

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

Status: Enrolling

Conditions: Asthma Acute

Treatments: Biological: blood sample

Study type: Interventional

Funder types: Other

Identifiers

NCT06015256

2022-A00651- 42 (Registry Identifier)

C21-75

Details and patient eligibility

About

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.

Enrollment: 448 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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)

Trial design

Primary purpose: Basic Science

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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448 participants in 4 patient groups

Severe uncontrolled asthma in exacerbation

Other group

Treatment:

Biological: blood sample

Severe uncontrolled asthma excluding exacerbation

Other group

Treatment:

Biological: blood sample

Severe controlled asthma

Other group

Treatment:

Biological: blood sample

Healthy volunteers (control group)

Other group

Treatment:

Biological: blood sample