Evidence map›Paper›PMID 36973953›Full record

ArticleClinical and translational allergy2023

Remibrutinib inhibits hives effector cells stimulated by serum from chronic urticaria patients independently of FcεR1 expression level and omalizumab clinical response.

Ramón Gimeno, Clara Ribas-Llauradó, David Pesque, Evelyn Andrades, Bruno Cenni, Barbara Ambros, Ramon Pujol, Ana M Giménez-Arnau

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational allergy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Towards Personalised Therapy in Chronic Spontaneous Urticaria: Advancing From Endotype to Clinical Response.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
    Review
  7. Current and future landscape of Bruton tyrosine kinase inhibitors in allergy.The Journal of allergy and clinical immunology · 2025
    Review
  8. Autoallergy and what the Allergist Needs to know.Current allergy and asthma reports · 2025
    Review
  9. Review
  10. Review
  11. Bruton's tyrosine kinase inhibition for the treatment of allergic disorders.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2024
    Review
  12. Article
  13. Review
  14. Review
  15. 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 at 3 institutions in 2 countries.

Ramón GimenoLaboratory of Immunology, Department of Pathology, Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-8758-121X
Clara Ribas-LlauradóDepartment Immnology, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0001-7179-1290
David PesqueDepartment of Dermatology, Hospital del Mar, IMIM, Universitat Pompeu Fabra, Barcelona, Spain.ORCID https://orcid.org/0000-0002-5821-9780
Evelyn AndradesDepartment Immnology, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Bruno CenniDepartment of Research, BC Novartis Institutes for BioMedical Research, Novartis, Basel, Switzerland.
Barbara AmbrosDepartment of Clinical Development, BA Global Drug Development, Novartis, Basel, Switzerland.
Ramon PujolDepartment Immnology, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-5622-6055
Ana M Giménez-ArnauDepartment Immnology, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0001-5434-7753
Universitat Pompeu Fabra · ESNovartis (Switzerland) · CHHospital Del Mar · ES

Funding

Instituto de Salud Carlos III PI17/00198Novartis
6 · The paper itself

Abstract

backgroundDespite advances in the treatment of chronic urticaria, in a significant percentage of the patients symptoms are not fully controlled with conventional approaches. New strategies under development include blocking intracellular mediators of mast cell and basophil activation.

objectiveWe aim to investigate the effects of the Bruton's tyrosine kinase (BTK) inhibitor remibrutinib on human blood basophils and CD34

methodsTwenty-two patients with chronic spontaneous urticaria (mean age 52 years, 27% women) and 22 patients with chronic inducible urticaria (46 years, 27% women) were included in the study together with a sex-matched control group. Patients were classified as responders or non-responders to anti-IgE therapy on the basis of their clinical data, FcεR1a expression on blood basophils and total IgE levels. Changes on CD63 expression-as an activation marker-, were used to evaluate in vitro the response of basophils and mast cells to serum exposure and the inhibitory effects of remibrutinib.

resultsRemibrutinib inhibits degranulation induced by IgE cross-linking in mast cells and basophils and also the activation triggered by factors present in the sera of spontaneous and inducible chronic urticaria patients. Patient's serum induces a greater degranulation of effector cells than controls. Activation of mast cells and basophils by patient sera and remibrutinib effects were not related to omalizumab responsiveness.

conclusionRemibrutinib inhibits activation of human basophils and mast cells induced in vitro by exposure to the serum of chronic urticaria patients independently of their response to omalizumab.

Indexed as

basophilsBruton's tyrosine kinasechronic urticariaIgEmast cellsomalizumabremibrutinib

Identifiers

PMID36973953
PMCPMC9985467
OpenAlexW4323074264

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.