%0 Journal Article
%T Nasal Brushing Molecular Endotyping Distinguishes CRSwNP Patients with Better Response to Dupilumab.
%A Gayvert K
%A Desrosiers M
%A Laidlaw TM
%A Mannent LP
%A Patel K
%A Horowitz J
%A Amin N
%A Jagerschmidt A
%A Hamilton JD
%A Lim WK
%A Harel S
%J J Allergy Clin Immunol
%V 0
%N 0
%D 2024 Jun 14
%M 38880251
%F 14.29
%R 10.1016/j.jaci.2024.05.030
%X <B>BACKGROUND: </B>There is evidence of pathophysiologic diversity in chronic rhinosinusitis with nasal polyps (CRSwNP), but data characterizing the molecular endotypes of CRSwNP and their association with treatment is lacking.<BR><B>OBJECTIVE: </B>To identify gene signatures associated with CRSwNP endotypes, clinical features, and dupilumab treatment response.<BR><B>METHODS: </B>Nasal brushing samples were collected from 89 patients randomized to dupilumab 300 mg every 2 weeks or placebo in the SINUS-52 trial (NCT02898454). Microarrays were used to identify transcriptional clusters and assess the relationship between gene expression and baseline clinical features and clinical response to dupilumab. Endotype signatures were determined using differential expression analysis.<BR><B>RESULTS: </B>Two distinct transcriptional clusters (C1 and C2) were identified, both with elevated type 2 biomarkers. At baseline, C2 patients had higher mean Nasal Polyp Score and higher type 2 biomarker levels than C1 patients. At Week 24, significant improvements in clinical outcomes (dupilumab vs placebo) were observed in both clusters, although the magnitude of improvements was significantly greater in C2 than C1, and more C2 patients demonstrated clinically meaningful responses. Gene sets enrichment analyses supported the existence of two molecular endotypes: C2 was enriched in genes associated with type 2 inflammation (including periostin, cadherin-26, and type 2 cysteine protease inhibitors), while C1 was enriched in genes associated with T cell activation and interleukin-12 production.<BR><B>CONCLUSIONS: </B>Two distinct gene signatures associated with CRSwNP clinical features were identified; the endotype signatures were associated with clinical outcome measures and magnitude of dupilumab response.