Hair follicle stem cell fate supports distinct clinical endotypes in hidradenitis suppurativa

作者
Audrey Onfroy,Francette Jean‐Louis,Philippe Le Corvoisier,Fanny Coulpier,Kévin Muret,Éric Bonnet,Raphaele Arrouasse,Caroline Boucle,Salwa Abid‐Essefi,É. Sbidian,Christina Bergqvist,P. Wolkenstein,Véronique Godot,Jean‐François Deleuze,Yves Lévy,Piotr Topilko,Étienne Audureau,Sophie Hüe
出处
标识
DOI:10.1111/jdv.70152
摘要

Abstract Background Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease affecting approximately 1% of the global population. Its pathogenesis involves both aberrant keratinization and autoinflammation, but the temporal relationship between these processes remains unclear. Objective To investigate the role of HF stem cell (HF‐SC) fate in the early pathogenesis of HS. Methods We performed single‐cell RNA sequencing of HF cell populations from HS patients and healthy donors. We then analysed HF cell composition isolated from perilesional skin of 49 HS patients and integrated these data with clinical phenotypes to define disease endotypes. Results Our data revealed two distinct differentiation trajectories of HF stem cells (HF‐SCs): one leading to interfollicular epidermis (IFE) basal cells enriched in inflammatory pathways, and another giving rise to outer root sheath (ORS) cells associated with keratinization. In HS lesions, both populations displayed altered inflammatory phenotypes and were closely linked to immune cell infiltration, pointing to a role in disease heterogeneity. By integrating clinical features with HF cell composition from 49 HS patients, we identified three major endotypes: (i) an inflammatory subtype, marked by T cell infiltration and an expansion of IFE basal cells; (ii) a keratinizing subtype, characterized by ORS enrichment and minimal inflammation; and (iii) a mixed subtype, exhibiting features of follicular remodelling, fistula formation and variable immune involvement. Conclusion These findings provide novel insights into the epithelial‐immune interactions that drive HS and support a stratified therapeutic approach tailored to distinct epithelial dysfunctions.
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