Evidence map›Paper›PMID 37624925›Full record

ReviewRheumatology (Oxford, England)2024

Differential properties of Janus kinase inhibitors in the treatment of immune-mediated inflammatory diseases.

Peter C Taylor, Ernest Choy, Xenofon Baraliakos, Zoltan Szekanecz, Ricardo M Xavier, John D Isaacs, Sander Strengholt, Julie M Parmentier, Ralph Lippe, Yoshiya Tanaka

Open access · hybridAbstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
18.6field-weighted citation impact, top 1% 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

60 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  4. Interleukin-6 fromMicrobiology spectrum · 2026
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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

10 authors at 10 institutions in 7 countries.

Peter C TaylorBotnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.ORCID 0000-0001-7766-6167
Ernest ChoyDivision of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0003-4459-8609
Xenofon BaraliakosRheumazentrum Ruhrgebiet Herne, Ruhr-University Bochum, Bochum, Germany.ORCID 0000-0002-9475-9362
Zoltan SzekaneczFaculty of Medicine, Department of Rheumatology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-7794-6844
Ricardo M XavierServiço de Reumatologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.ORCID 0000-0001-6570-4533
John D IsaacsTranslational and Clinical Research Institute, Newcastle University and Musculoskeletal Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Sander StrengholtAbbVie B.V., Mijdrecht, Utrecht, The Netherlands.
Julie M ParmentierImmunology Precision Medicine, AbbVie Bioresearch Center, Worcester, MA, USA.
Ralph LippeAbbVie Deutschland GmbH & Co. KG, Wiesbaden, Germany.
Yoshiya TanakaFirst Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.ORCID 0000-0002-0807-7139
AbbVie (Germany) · DEAbbVie (Netherlands) · NLAbbVie (United States) · USCardiff University · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBNuffield Orthopaedic Centre · GBRheumazentrum Ruhrgebiet · DEUniversidade Federal do Rio Grande do Sul · BRUniversity of Debrecen · HUUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Janus kinases (JAKs) are a family of cytosolic tyrosine kinases that regulate cytokine signal transduction, including cytokines involved in a range of inflammatory diseases, such as RA, psoriasis, atopic dermatitis and IBD. Several small-molecule JAK inhibitors (JAKis) are now approved for the treatment of various immune-mediated inflammatory diseases. There are, however, key differences between these agents that could potentially translate into unique clinical profiles. Each JAKi has a unique chemical structure, resulting in a distinctive mode of binding within the catalytic cleft of the target JAK, and giving rise to distinct pharmacological characteristics. In addition, the available agents have differing selectivity for JAK isoforms, as well as off-target effects against non-JAKs. Other differences include effects on haematological parameters, DNA damage repair, reproductive toxicity and metabolism/elimination. Here we review the pharmacological profiles of the JAKis abrocitinib, baricitinib, filgotinib, peficitinib, tofacitinib and upadacitinib.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidJanus Kinase InhibitorsPsoriasisHumansJanus KinasesAntirheumatic AgentsJanus Kinase InhibitorsJanus Kinasesabrocitinibbaricitinibfilgotinibmode of actionpeficitinibtofacitinibupadacitinib

Identifiers

PMID37624925
PMCPMC10836981
OpenAlexW4386156879

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.