Evidence map›Paper›PMID 40063233›Full record

ArticleClinical rheumatology2025

Anti-CD74 autoantibodies in axial spondyloarthritis as biomarkers for activity and severity of disease but not for tumour necrosis factor inhibitor retention: data from the Swiss Clinical Quality Management in rheumatic diseases cohort.

Annik Steimer, Andrea Götschi, Torsten Witte, Almut Scherer, Jonas Brändli, Michael J Nissen, Burkhard Möller, Simon Grosswiler, Diego Kyburz, Diana Dan and 5 more

Abstract read
In one paragraph

Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

15 authors.

Annik SteimerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland. annik.steimer@usz.ch.ORCID http://orcid.org/0009-0009-5896-2230
Andrea GötschiSwiss Clinical Quality Management Foundation, Zurich, Switzerland.
Torsten WitteDepartment of Rheumatology and Immunology, Hannover Medical School, Hannover, Germany.
Almut SchererSwiss Clinical Quality Management Foundation, Zurich, Switzerland.
Jonas BrändliSwiss Clinical Quality Management Foundation, Zurich, Switzerland.
Michael J NissenDepartment of Rheumatology, Geneva University Hospital, Geneva, Switzerland.
Burkhard MöllerDepartment of Rheumatology and Immunology, Inselspital, Bern, Switzerland.
Simon GrosswilerSwiss Ankylosing Spondylitis Association, Zurich, Switzerland.
Diego KyburzDepartment of Rheumatology, University Hospital Basel, University of Basel, Basel, Switzerland.
Diana DanDepartment of Rheumatology, Lausanne University Hospital (CHUV), University of Lausanne, Lausanne, Switzerland.
Andrea Rubbert-RothDepartment of Rheumatology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Sabine AdlerDepartment of Rheumatology, Cantonal Hospital Aarau, Aarau, Switzerland.
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Xenofon BaraliakosRheumazentrum Ruhrgebiet Herne, Ruhr-University Bochum, Bochum, Germany.
Adrian CiureaDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAnti-CD74 antibodies (Abs) have been proposed as a diagnostic biomarker in axial spondyloarthritis (axSpA). The aims of this study were to evaluate the association of these Abs with disease activity parameters in axSpA and to assess their predictive value for tumour necrosis factor inhibitor (TNFi) treatment effectiveness.

methodsPatients diagnosed with axSpA in the Swiss Clinical Quality Management registry with available biosamples and a measurement of IgA anti-CD74 Abs were included in this cohort study. We used a cut-off of 15 U/ml to define anti-CD74 Abs elevation. Associations of important disease characteristics with anti-CD4 Abs elevation and anti-CD74 Abs levels were evaluated using logistic and linear regression, respectively. For patients with an available biosample before TNFi initiation, we evaluated drug retention and estimated the hazard ratio of treatment discontinuation depending on anti-CD74 Abs elevation.

resultsElevated IgA anti-CD74 Abs were found in 383/722 (53%) patients with axSpA and were significantly associated with older age, male sex, and elevated C-reactive protein (CRP). Among 310 patients starting TNFi treatment, no significant difference in drug retention was found between patients with and without elevated anti-CD74 Abs (HR 0.91, 95% CI 0.66 to 1.25). An increased Bath Ankylosing Spondylitis Disease Activity Index was found to be associated with a reduced TNFi retention whereas an elevated CRP was associated with a prolonged retention.

conclusionsAlthough elevated IgA anti-CD74 Abs are associated with CRP elevation, we could not demonstrate an additional value of this biomarker for predicting response to treatment with TNFi beyond CRP measurement.

Indexed as

Antigens, Differentiation, B-LymphocyteAutoantibodiesAxial SpondyloarthritisHistocompatibility Antigens Class IITumor Necrosis Factor InhibitorsAdultBiomarkersCohort StudiesC-Reactive ProteinFemaleHumansImmunoglobulin AMaleMiddle AgedRegistriesSeverity of Illness IndexAntigens, Differentiation, B-LymphocyteAutoantibodiesBiomarkersC-Reactive ProteinHistocompatibility Antigens Class IIImmunoglobulin Ainvariant chainTumor Necrosis Factor InhibitorsAxial spondyloarthritisCohort studyIgA anti-CD74 antibodiesTNF inhibitor treatment

Identifiers

PMID40063233
PMCPMC11993484

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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.