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.
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.
Study Type
OBSERVATIONAL
Enrollment
34
Collection of one tube of 7.5 ml blood in addition to a blood sample made in clinical practice
Collection of five tubes of 7.5 ml blood in addition to a blood sample made in clinical practice
Larrey hospital
Toulouse, France
Frequency of circulating ILC2 between gender with asthma.
Estimation of the proportion of circulating ILC2 between males and females with asthma.
Time frame: Day 1
Frequency of circulating ILC2 according to asthma severity.
Estimation of the proportion of circulating ILC2 between mild to moderate asthma patients and severe asthma patients.
Time frame: Day 1
Comparison of the effect of (androgenic receptor) AR ligands in a culture of ILC2.
ILC2 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.
Time frame: Day 1
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.