Evidence map›Paper›PMID 39188724›Full record

ArticleFrontiers in immunology2024

The JAK1/JAK2 inhibitor ruxolitinib inhibits mediator release from human basophils and mast cells.

Remo Poto, Leonardo Cristinziano, Gjada Criscuolo, Caterina Strisciuglio, Francesco Palestra, Gianluca Lagnese, Antonio Di Salvatore, Gianni Marone, Giuseppe Spadaro, Stefania Loffredo and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. The Potential Role ofMicroorganisms · 2025
    Review
  9. Review
  10. Article
  11. Allergen Immunotherapy: Pitfalls, Perks and Unexpected Allies.International journal of molecular sciences · 2025
    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

11 authors.

Remo PotoDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Leonardo CristinzianoDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gjada CriscuoloDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Caterina StrisciuglioDepartment of Woman, Child and General and Specialistic Surgery, University of Campania "Luigi Vanvitelli", Naples, Italy.
Francesco PalestraDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gianluca LagneseDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Antonio Di SalvatoreDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gianni MaroneDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Giuseppe SpadaroDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Stefania LoffredoDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Gilda VarricchiDepartment of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The Janus kinase (JAK) family includes four cytoplasmic tyrosine kinases (JAK1, JAK2, JAK3, and TYK2) constitutively bound to several cytokine receptors. JAKs phosphorylate downstream signal transducers and activators of transcription (STAT). JAK-STAT5 pathways play a critical role in basophil and mast cell activation. Previous studies have demonstrated that inhibitors of JAK-STAT pathway blocked the activation of mast cells and basophils. Methods: In this study, we investigated the Results: Ruxolitinib concentration-dependently inhibited IgE-mediated release of preformed (histamine) and Discussion: These results indicate that ruxolitinib, inhibiting the release of several mediators from human basophils and mast cells, is a potential candidate for the treatment of inflammatory disorders.

Indexed as

BasophilsJanus Kinase 1Janus Kinase 2Mast CellsNitrilesPyrazolesPyrimidinesCells, CulturedCytokinesHumansImmunoglobulin EJanus Kinase InhibitorsProtein Kinase InhibitorsCytokinesImmunoglobulin EJAK1 protein, humanJAK2 protein, humanJanus Kinase 1Janus Kinase 2Janus Kinase InhibitorsNitrilesProtein Kinase InhibitorsPyrazolesPyrimidinesruxolitinibasthmabasophilhistamineIL-13IL-4mast cellpolycythemia veraruxolitinib

Identifiers

PMID39188724
PMCPMC11345246

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.