Evidence map›Paper›PMID 41194923›Full record

ArticleFrontiers in immunology2025

The effect of baricitinib on pSTAT3 levels in IL-6- or IL-15-stimulated PBMCs isolated from patients with SLE.

Gábor J Szebeni, Nikolett Gémes, Patrícia Neuperger, Enikő Szabó, József Á Balog, Dániel Honfi, Attila Balog, Gergely Toldi

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

8 authors.

Gábor J Szebeni *Laboratory of Functional Genomics, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
Nikolett Gémes *Laboratory of Functional Genomics, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
Patrícia NeupergerLaboratory of Functional Genomics, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
Enikő SzabóLaboratory of Functional Genomics, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
József Á BalogLaboratory of Functional Genomics, Core Facility, HUN-REN Biological Research Centre, Szeged, Hungary.
Dániel HonfiDepartment of Rheumatology and Immunology, Faculty of Medicine, Albert Szent-Gyorgyi Health Centre, University of Szeged, Szeged, Hungary.
Attila Balog *Department of Rheumatology and Immunology, Faculty of Medicine, Albert Szent-Gyorgyi Health Centre, University of Szeged, Szeged, Hungary.
Gergely Toldi *Department of Rheumatology and Immunology, Faculty of Medicine, Albert Szent-Gyorgyi Health Centre, University of Szeged, Szeged, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease marked by multi-organ inflammation. Its pathogenesis involves profound T-cell dysfunction, autoreactive B-cell activation, impaired CD8 Methods: We aimed to investigate STAT3 phosphorylation in CD4 Results: Despite long-term immunomodulators, significant STAT3 activation was observed in T cells and myeloid cells upon IL-6 or IL-15 stimulation in patients with SLE. Baricitinib effectively inhibited STAT3 phosphorylation in these cell types, though its inhibitory effect was notably weaker following IL-15 stimulation compared to IL-6. Notably, baricitinib did not affect the proportion of interferon-γ (IFN-γ)- or IL-17-expressing cells. Conclusion: These findings highlight the cell-type and cytokine-specific effects of baricitinib and demonstrate its capacity to dampen IL-6- and IL-15-mediated STAT3 activation in key immune cell subsets. Our results support a precision medicine approach to JAK inhibition in SLE and reinforce the potential of baricitinib in modulating key inflammatory pathways.

Indexed as

AzetidinesInterleukin-15Interleukin-6Leukocytes, MononuclearLupus Erythematosus, SystemicPurinesPyrazolesSTAT3 Transcription FactorSulfonamidesAdultFemaleHumansMaleMiddle AgedPhosphorylationSignal TransductionAzetidinesbaricitinibIL6 protein, humanInterleukin-15Interleukin-6PurinesPyrazolesSTAT3 protein, humanSTAT3 Transcription FactorSulfonamidesbaricitinibJAK/STAT pathwaymulticolor flow cytometrypSTAT3systemic lupus erythematosus

Identifiers

PMID41194923
PMCPMC12583204

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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.