Evidence map›Paper›PMID 41705342›Full record

Trial reportAllergy2026

Integrated Clinical Trial and Molecular Profiling Reveals Immune Drivers of Chronic Hand Eczema.

Perrine Gery, Rüçhan Ekren, Emilie Bérard, Aurélie Du-Thanh, Hugo Rimet, Fatma Jendoubi, Vanina Lenief, Nadia Raison-Peyron, Amel Bouznad, Maria P Konstantinou and 16 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

26 authors.

Perrine GeryCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.
Rüçhan EkrenInfinity (Institut Toulousain des Maladies Infectieuses et Inflammatoires), Immception Lab, Inserm U1291, Toulouse University, Toulouse, France.ORCID https://orcid.org/0000-0001-6737-7281
Emilie BérardDepartment of Clinical Epidemiology and Public Health, Toulouse University Hospital, Toulouse, France.
Aurélie Du-ThanhDepartment of Dermatology, Saint-Eloi Hospital, Montpellier University, Montpellier, France.
Hugo RimetCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.ORCID https://orcid.org/0009-0008-7995-8903
Fatma JendoubiDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.
Vanina LeniefCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.
Nadia Raison-PeyronDepartment of Dermatology, Saint-Eloi Hospital, Montpellier University, Montpellier, France.ORCID https://orcid.org/0000-0002-7991-3165
Amel BouznadDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.
Maria P KonstantinouDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.
Jonathan RioualDepartment of Clinical Epidemiology and Public Health, Toulouse University Hospital, Toulouse, France.
Lilian BassoInfinity (Institut Toulousain des Maladies Infectieuses et Inflammatoires), Immception Lab, Inserm U1291, Toulouse University, Toulouse, France.ORCID https://orcid.org/0000-0002-2816-1557
Juliette MouirenCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.
Manon BoussierDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.
Brigitte MilpiedCHU de Bordeaux, Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, UMR 5164, Bordeaux, France.
Cristina Bulai LivideanuDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.ORCID https://orcid.org/0000-0002-5275-6868
Louise JaulentDepartment of Allergology and Clinical Immunology, Hospices Civils de Lyon, Lyon Sud Hospital, Pierre-Bénite, France.
Florence HacardDepartment of Allergology and Clinical Immunology, Hospices Civils de Lyon, Lyon Sud Hospital, Pierre-Bénite, France.
Marine A LefevreCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.
Audrey NosbaumCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.
Julien SeneschalCHU de Bordeaux, Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, UMR 5164, Bordeaux, France.
Marc VocansonCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.ORCID https://orcid.org/0000-0002-0181-8862
Carle PaulDepartment of Dermatology, Larrey Hospital, Toulouse University, Toulouse, France.
Nicolas GaudenzioInfinity (Institut Toulousain des Maladies Infectieuses et Inflammatoires), Immception Lab, Inserm U1291, Toulouse University, Toulouse, France.ORCID https://orcid.org/0000-0002-5648-509X
Marie TauberCentre International de Recherche en Infectiologie, University of Lyon 1 and École Normale Supérieure de Lyon, Inserm U1111, Lyon, France.ORCID https://orcid.org/0000-0001-6245-7442
French Atopic Dermatitis Network from de GREAT Research group

Funding

Acteria FundationAgence Nationale de la RechercheEuropean Research CouncilSanofi US ISS
6 · The paper itself

Abstract

backgroundChronic hand eczema (CHE) is a debilitating skin condition characterized by pain, itch, and chronic inflammation, with a complex multifactorial origin. Its diverse presentations, including overlapping traits of atopic dermatitis, contact dermatitis, and psoriasis, make diagnosis and treatment particularly challenging. The underlying immune mechanisms of CHE still need to be investigated.

methodsHere we conducted a comprehensive molecular profiling of CHE patients, enrolled without prior selection on etiology and morphology, and performed a phase 2b randomized, multicenter, double-blind, placebo-controlled clinical trial comparing dupilumab to placebo over 16 weeks.

resultsWe demonstrated that CHE patients may benefit from IL4Rα-blockade, regardless of etiological factors or clinical presentation. Skin transcriptomic and serum profiles of CHE patients closely resemble those seen in both atopic dermatitis and psoriasis, with dysregulated genes affecting keratinocyte differentiation, leucocyte-mediated immunity, cytokine signaling, and mixed type 1, 2, and 3 immunity. The clinical trial included 94 adults with moderate to severe CHE persisting for at least six months and resistant to potent topical corticosteroids. Compared to placebo control, 16-week dupilumab treatment significantly improved clinical severity and quality of life of all CHE patients while largely restoring appropriate transcriptomic and proteomic programs related to skin barrier and immune homeostasis.

conclusionThese findings confirmed the involvement of not only type 2 but also type 1 and type 3 immunity across all CHE patients, and demonstrate that IL-4Rα blockade may offer effective therapeutic perspectives for this highly burdensome condition, independent of an atopic dermatitis background.

Indexed as

EczemaHand DermatosesAdultAntibodies, Monoclonal, HumanizedBiomarkersChronic DiseaseDouble-Blind MethodFemaleGene Expression ProfilingHumansInterleukin-4 Receptor alpha SubunitMaleMiddle AgedQuality of LifeTranscriptomeTreatment OutcomeAntibodies, Monoclonal, HumanizedBiomarkersdupilumabInterleukin-4 Receptor alpha Subunitchronic hand eczemadupilumabmixed immune signaturemolecular profilingrandomized clinical trial

Identifiers

PMID41705342
PMCPMC13465994

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Registered trials

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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 OpenQuestion graph.