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Analysis of Sexual Bias in Type 2 Innate Lymphoid Cells (ILC2) in Asthmatic Patients

Analysis of Sexual Bias in Type 2 Innate Lymphoid Cells (ILC2) in Asthmatic Patients: Role of Androgens

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04384835
Acronym
IL-C2
Enrollment
34
Registered
2020-05-12
Start date
2021-03-08
Completion date
2023-04-12
Last updated
2023-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

allergy, type 2 innate lymphoid cells

Brief summary

Asthma is more common in females than in males but the difference has not been explained yet. Group 2 innate lymphoid cells (ILC2) have recently emerged as critical players in the initiation of allergic responses but their implications in the difference between males and females in terms of asthma prevalence has not been fully studied. The aim of this project is to compare the proportion of ILC2 in blood between males and females with asthma.

Detailed description

Asthma is more common in males until puberty but becomes more prevalent and more severe in females after puberty suggesting a protective action of male sex hormones. ILC2 have recently emerged as critical players in the initiation of allergic responses. The present team established that androgens, signaling through the nuclear receptor 3 C4 (NR3C4) androgen receptor (AR), negatively control ILC2 at steady state and during lung inflammation. Relevant to this application, females with asthma have more circulating ILC2 than males. The present hypothesis is that harnessing AR signaling in ILC2 may provide a new therapeutic approach to down regulate tissue resident ILC2. This project will analyze the sex bias in circulating ILC2 in female and male patients with moderate to severe asthma. In females with asthma, the team will purify circulating ILC2 from peripheral blood mononuclear cells (PBMC) and expand them in vitro using cytokines and stromal cells in the presence of AR antagonist or agonist ligands. Bulk ILC2 cultures at day 7 will used to measure the expression profile of various gene, including AR.

Interventions

BIOLOGICALBlood sample collection (one tube)

Collection of one tube of 7.5 ml blood in addition to a blood sample made in clinical practice

BIOLOGICALBlood sample collection (five tubes)

Collection of five tubes of 7.5 ml blood in addition to a blood sample made in clinical practice

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Asthma according to the criteria described by Global Initiative for Asthma (GINA) guidelines * Severe asthma according to the criteria described by the American Thoracic Society (ATS) / European Respiratory Society (ERS) guidelines (for the recruitment of severe patients) * Mild to moderate asthma based on low or medium dose of inhaled steroids according to GINA guidelines

Exclusion criteria

* Asthma exacerbations defined as oral corticosteroids related to worsening respiratory symptoms within the past 4 weeks * Pregnant women * Breastfeeding women * Autoimmune diseases * Androgen medication * Early menopause defined as the absence of menstruation for at least 1 year * Body mass index ≥ 30 kg/m² * Weight \<40 kg * Oral corticotherapy for more than 3 months * Prediction of blood volume collected (care + research)\> 80 ml or\> 150 ml over a period of 30 days if blood collection within the past 30 days * known anemia with hemoglobin \<10 g/dl

Design outcomes

Primary

MeasureTime frameDescription
Frequency of circulating ILC2 between gender with asthma.Day 1Estimation of the proportion of circulating ILC2 between males and females with asthma.

Secondary

MeasureTime frameDescription
Frequency of circulating ILC2 according to asthma severity.Day 1Estimation of the proportion of circulating ILC2 between mild to moderate asthma patients and severe asthma patients.
Comparison of the effect of (androgenic receptor) AR ligands in a culture of ILC2.Day 1ILC2 purified form PBMC of asthmatic females will be expanded in vitro in the presence of AR antagonist or agonist ligands. Bulk ILC2 cultures at day 7 will used to measure the expression profile of various gene, including AR.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026