Evidence map›Paper›PMID 40076933›Full record

ReviewInternational journal of molecular sciences2025

Bimekizumab in the Treatment of Axial Spondyloarthritis and Psoriatic Arthritis: A New Kid on the Block.

Julie Sarrand, Laurie Baglione, Charlotte Bouvy, Muhammad Soyfoo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. 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

4 authors.

Julie SarrandDepartment of Rheumatology, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, 1070 Bruxelles, Belgium.ORCID 0000-0002-6833-0044
Laurie BaglioneDepartment of Rheumatology, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, 1070 Bruxelles, Belgium.
Charlotte BouvyDepartment of Rheumatology, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, 1070 Bruxelles, Belgium.
Muhammad SoyfooDepartment of Rheumatology, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, 1070 Bruxelles, Belgium.ORCID 0000-0002-9051-1810

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interleukin (IL)-17 family encompasses six structurally related pro-inflammatory cystine knot proteins, designated as IL-17A to IL-17F. Over the last decades, evidence has pointed to its role as a critical player in the development of inflammatory diseases such as psoriasis (PsO), axial spondyloarthritis (axSpA), and psoriatic arthritis (PsA). More specifically, IL-17A and IL-17F are overexpressed in the skin and synovial tissues of patients with these diseases, and recent studies suggest their involvement in promoting inflammation and tissue damage in axSpA and PsA. Bimekizumab is a monoclonal antibody targeting both IL-17A and IL-17F, playing an important role in the treatment of these diseases. This review details the implications of bimekizumab in the therapeutic armamentarium of axSpA and PsA.

Indexed as

Antibodies, Monoclonal, HumanizedArthritis, PsoriaticAxial SpondyloarthritisAnimalsHumansInterleukin-17Antibodies, Monoclonal, HumanizedbimekizumabInterleukin-17axial spondyloarthritis (axSpA)bimekizumabcytokinesIL-17AIL-17Finflammationinterleukin-17 (IL-17)psoriasis (PsO)psoriatic arthritis (PsA)

Identifiers

PMID40076933
PMCPMC11899827

What OpenQuestion holds

Textmetadata
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.