Evidence map›Paper›PMID 42089905›Full record

Observational studyRheumatology international2026

Apremilast therapy increases CD39

Athanasios Mavropoulos, Sotirios G Tsiogkas, Theodora Simopoulou, Efthimios Dardiotis, Efterpi Zafiriou, Lazaros I Sakkas, Dimitrios P Bogdanos

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology international, 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

7 authors.

Athanasios Mavropoulos *Department of Rheumatology and Clinical Immunology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0002-5328-1323
Sotirios G Tsiogkas *Department of Rheumatology and Clinical Immunology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0001-8900-7281
Theodora SimopoulouDepartment of Rheumatology and Clinical Immunology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0003-2604-5090
Efthimios DardiotisDepartment of Neurology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0003-2957-641X
Efterpi ZafiriouDepartment of Dermatology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0002-6594-7292
Lazaros I SakkasDepartment of Rheumatology and Clinical Immunology, Faculty of Medicine, University of Thessaly, Larissa, Greece.ORCID http://orcid.org/0000-0002-7670-3314
Dimitrios P BogdanosDepartment of Rheumatology and Clinical Immunology, Faculty of Medicine, University of Thessaly, Larissa, Greece. bogdanos@med.uth.gr.ORCID http://orcid.org/0000-0002-9697-7902

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis and psoriatic arthritis (PsA) are chronic inflammatory diseases, recognized as one entity, termed psoriatic disease (PsD). CD39 is an ectonucleotidase that hydrolyzes ATP to adenosine and is expressed on a human Treg sub-population capable of exerting interleukin (IL-) 17 suppression. We aimed to investigate the effect of apremilast on CD39 expression in T cells from patients with PsD. Peripheral blood mononuclear cells (PBMCs) were analyzed by multicolor flow cytometry and appropriate monoclonal antibodies. Intracellular cytokine production of PBMCs was measured after in vitro PMA plus ionomycin stimulation. At 6 weeks post-treatment, apremilast inhibited IL-17 and interferon-γ (IFNγ) production, increased IL-10 production in both CD4+T cells and CD4-T cells, and inhibited IL-6 production in CD4-T cells. At baseline, levels of CD4+CD39+ cells were decreased in patients compared to controls. At 6 weeks post-treatment, CD4+CD39+ cells increased. Furthermore, CD4+CD39+ cells producing IL-10 increased in patients who achieved a PASI response. A significant proportion of IL-10-producing CD39+ cells were CD56-CD11c- cells. CD4+FoxP3+ cells were decreased in patients compared to controls. At 6 weeks post-treatment CD4+FoxP3+ cells, and CD4+FoxP3+CD39+ cells increased, although CD4+CD25hiFoxP3+ Treg cells did not change significantly. If confirmed in larger studies, CD4+CD39+ cells producing IL-10 could likely become associated with the response to apremilast.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalApyraseCD4-Positive T-LymphocytesPsoriasisThalidomideAdultAntigens, CDFemaleForkhead Transcription FactorsHumansInterleukin-10MaleMiddle AgedPilot ProjectsRetrospective StudiesT-Lymphocytes, RegulatoryAntigens, CDAnti-Inflammatory Agents, Non-SteroidalapremilastApyraseCD39 antigenENTPD1 protein, humanForkhead Transcription FactorsFOXP3 protein, humanIL10 protein, humanInterleukin-10ThalidomideApremilastArthritis, PsoriaticBlood Cells, MononuclearEctonucleoside Triphosphate Diphosphohydrolase 1 (CD39)Flow CytometryFOXP3 protein, humanInterleukin-10PsoriasisT-Lymphocytes, Regulatory

Identifiers

PMID42089905
PMCPMC13149556

What OpenQuestion holds

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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.