Evidence map›Paper›PMID 42625606›Full record

ArticleFrontiers in immunology2026

The evaluation of cytokine profiles in atopic dermatitis patients treated with dupilumab: association with ocular complications.

Jarmila Čelakovská, Eva Čermáková, Petra Boudkova, Ctirad Andrýs

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Jarmila ČelakovskáDepartment of Dermatology and Venereology Faculty Hospital and Medical Faculty of Charles University, Hradec Králové, Czechia.
Eva ČermákováDepartment of Medical Biophysics, Medical Faculty of Charles University, Hradec Králové, Czechia.
Petra BoudkovaDepartment of Clinical Immunology and Allergy, Faculty Hospital and Medical Faculty of Charles University, Hradec Králové, Czechia.
Ctirad AndrýsDepartment of Clinical Immunology and Allergy, Faculty Hospital and Medical Faculty of Charles University, Hradec Králové, Czechia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dupilumab is an effective treatment for moderate-to-severe atopic dermatitis (AD), yet a substantial proportion of patients develop ocular complications collectively termed dupilumab-associated ocular surface disease (DAOSD). Despite multiple proposed mechanisms - including goblet cell depletion, mucin deficiency, Th1/Th17 immune shifts, and microbiome alterations - no upstream epithelial cytokine marker has been clearly identified. Objective: To evaluate whether plasma cytokines differ between AD patients treated with dupilumab who develop ocular complications and those without ocular involvement. Methods: Complex dermatological examination was performed in adult AD patients receiving dupilumab for ≥24 months. Plasma cytokines (IFN-γ, TNF-α, IL-23, IL-2, IL-31, IL-6, IL-17A, IL-17E, IL-12p70, TSLP, IL-4, IL-5, IL-13, IL-10, IL-33) were quantified under unstimulated and PMA/ionomycin-stimulated conditions in winter and summer seasons. Differences between groups were assessed using non-parametric tests (Mann-Whitney U test and Kolmogorov-Smirnov test). To account for multiple comparisons across the large number of tested cytokines, false discovery rate (FDR) correction was performed using the Benjamini-Hochberg procedure with a significance threshold of q = 0.05. Receiver operating characteristic (ROC) analysis was performed to evaluate biomarker potential to explore potential discriminative performance. AUC values were calculated using empirical (non-parametric) ROC analysis. Results: During the summer period, stimulated thymic stromal lymphopoietin (TSLP) levels were nominally higher in patients with ocular complications compared with those without (p = 0.045). However, this difference did not remain statistically significant after FDR correction. In winter, stimulated TSLP showed a non-significant trend toward higher levels (p = 0.088). No other cytokines differed between groups. ROC analysis demonstrated moderate discriminative ability of stimulated TSLP (AUC 0.81 in summer; 0.70 in winter), although confidence intervals were wide. Conclusion: Stimulated TSLP may represent a preliminary observation requiring confirmation in dupilumab-treated AD patients with ocular complications.

Indexed as

Antibodies, Monoclonal, HumanizedCytokinesDermatitis, AtopicAdultBiomarkersFemaleHumansMaleMiddle AgedYoung AdultAntibodies, Monoclonal, HumanizedBiomarkersCytokinesdupilumabatopic dermatitisblepharitisconjunctivitiscytokinesdupilumabdupilumab complicationskeratitisocular inflammation

Identifiers

PMID42625606
PMCPMC13489922

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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.