Evidence map›Paper›PMID 41195937›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2026

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

Audrey Onfroy, Francette Jean-Louis, Philippe Le Corvoisier, Fanny Coulpier, Kévin Muret, Eric Bonnet, Raphaele Arrouasse, Caroline Boucle, Salwa Abid, Emilie Sbidian and 8 more

Abstract read
In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Hair follicle stem cell fate supports distinct clinical endotypes in hidradenitis suppurativa.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Audrey OnfroyINSERM U955-Team 9, Institut Mondor de Recherche Biomédicale (IMRB), Université Paris-Est Créteil (UPEC), Créteil, France.ORCID https://orcid.org/0009-0003-1429-4230
Francette Jean-LouisINSERM U955-Team 9, Institut Mondor de Recherche Biomédicale (IMRB), Université Paris-Est Créteil (UPEC), Créteil, France.ORCID https://orcid.org/0000-0001-7438-4906
Philippe Le CorvoisierINSERM, Clinical Investigation Center 1430, AP-HP, DMU Saphire, Henri Mondor University Hospital, Créteil, France.
Fanny CoulpierINSERM U955-Team 9, Institut Mondor de Recherche Biomédicale (IMRB), Université Paris-Est Créteil (UPEC), Créteil, France.ORCID https://orcid.org/0000-0002-1558-0293
Kévin MuretInstitut de Biologie François Jacob, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, Evry, France.ORCID https://orcid.org/0000-0003-3988-7772
Eric BonnetInstitut de Biologie François Jacob, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, Evry, France.ORCID https://orcid.org/0000-0002-8468-2867
Raphaele ArrouasseINSERM, Clinical Investigation Center 1430, AP-HP, DMU Saphire, Henri Mondor University Hospital, Créteil, France.ORCID https://orcid.org/0009-0006-5884-3125
Caroline BoucleINSERM, Clinical Investigation Center 1430, AP-HP, DMU Saphire, Henri Mondor University Hospital, Créteil, France.
Salwa AbidINSERM U955-Team 9, Institut Mondor de Recherche Biomédicale (IMRB), Université Paris-Est Créteil (UPEC), Créteil, France.ORCID https://orcid.org/0000-0002-4965-5855
Emilie SbidianINSERM, Clinical Investigation Center 1430, AP-HP, DMU Saphire, Henri Mondor University Hospital, Créteil, France.ORCID https://orcid.org/0000-0002-1267-5270
Christina BergqvistEpiDermE EA 7379, Université Paris Est Créteil, Créteil, France.ORCID https://orcid.org/0000-0003-4985-6785
Pierre WolkensteinINSERM, Clinical Investigation Center 1430, AP-HP, DMU Saphire, Henri Mondor University Hospital, Créteil, France.ORCID https://orcid.org/0000-0001-8194-457X
Véronique GodotVaccine Research Institute (VRI), Créteil, France.ORCID https://orcid.org/0000-0003-3557-308X
Jean-François DeleuzeInstitut de Biologie François Jacob, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), Université Paris-Saclay, Evry, France.ORCID https://orcid.org/0000-0002-5358-4463
Yves LévyVaccine Research Institute (VRI), Créteil, France.ORCID https://orcid.org/0000-0002-5549-6256
Piotr TopilkoINSERM U955-Team 9, Institut Mondor de Recherche Biomédicale (IMRB), Université Paris-Est Créteil (UPEC), Créteil, France.ORCID https://orcid.org/0000-0001-7381-6770
Etienne AudureauPublic Health Department, APHP, Hospital Henri-Mondor, Créteil, France.ORCID https://orcid.org/0000-0002-6166-149X
Sophie HueVaccine Research Institute (VRI), Créteil, France.ORCID https://orcid.org/0000-0002-2530-7346

Funding

Agence Nationale de la Recherche ANR-20-CE17-0019Institut National de la Santé et de la Recherche MédicaleSociété Française de Dermatologie et de Pathologie Sexuellement TransmissibleUniversité Paris-Est Créteil Val-de-Marne
6 · The paper itself

Abstract

backgroundHidradenitis 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.

objectivesTo investigate the role of HF stem cell (HF-SC) fate in the early pathogenesis of HS.

methodsWe 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.

resultsOur 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.

conclusionsThese findings provide novel insights into the epithelial-immune interactions that drive HS and support a stratified therapeutic approach tailored to distinct epithelial dysfunctions.

Indexed as

Hair FollicleHidradenitis SuppurativaStem CellsAdultCell DifferentiationFemaleHumansMaleMiddle AgedPhenotypeendotypeshair follicle cellshidradenitis suppurativainflammation

Identifiers

PMID41195937
PMCPMC12933698

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.