Leptin May Promote Eosinophilic CRSwNP Progression by Enhancing Eosinophil Chemotaxis and Angiogenesis Under a Type 2 Inflammatory Milieu.

BACKGROUND

Chronic rhinosinusitis with nasal polyp (CRSwNP) is a heterogeneous Type 2 inflammatory disease characterized by enhanced eosinophilic infiltration. Both innate and adaptive immunity are involved in the onset and progression of CRSwNP. Increased serum leptin levels are associated with various allergic conditions; however, the biological role of leptin in allergic immune cells requires further investigation.

OBJECTIVE

To investigate the effects of leptin on immune cells, including eosinophils, basophils, and mast cells, in CRSwNP.

METHODS

Leptin was used to stimulate eosinophils and eosinophilic cell lines, followed by analyses of gene expression, migration, and angiogenic capacity. Immunometabolic profile of CRSwNP, serum leptin, and galectin-10 levels were analyzed in conjunction with the gene expression profiles of nasal polyps. Furthermore, the biological effects of leptin on eosinophils were assessed using RNA sequencing and functional analyses, including a transwell migration assay and an angiogenesis assay via co-culture with human umbilical vein endothelial cells (HUVEC).

RESULTS

Increased serum leptin and galectin-10 levels were associated with Type 2 inflammatory markers and correlated with CRSwNP severity. RNA sequencing revealed upregulation of chemokine ligands in eosinophilic cell lines. Leptin induced plasminogen activator inhibitor 1 (PAI-1) expression in eosinophils but not in basophils or neutrophils. Leptin pretreatment substantially enhanced migration toward both C-C motif chemokine ligand (CCL) 11 and CCL26 in eosinophilic cell lines. The leptin-primed eosinophilic cell line promoted angiogenesis, as demonstrated in co-culture with HUVECs.

CONCLUSION

Leptin promotes eosinophil migration and angiogenesis, potentially via chemokine ligands and PAI-1 induction, and may promote CRSwNP progression under a Type 2 inflammatory milieu.