Evidence map›Paper›PMID 42481524›Full record

ArticleNature communications2026

Towards a proteomic plasma biomarker panel for diagnosing vasculitis remission.

Uwe Jerke, Marieluise Kirchner, Theda Up Bartolomaeus, Lovis Kling, Vojtech Kratky, Zdenka Hruskova, Vladimir Tesar, Kai-Uwe Eckardt, Adrian Schreiber, Sofia Forslund and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2026. 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

12 authors.

Uwe Jerke *Experimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany.
Marieluise Kirchner *Core Unit Proteomics, Berlin Institute of Health (BIH), Charité and MDC, Berlin, Germany.ORCID 0000-0002-7049-534X
Theda Up Bartolomaeus *Experimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany.
Lovis KlingExperimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany.ORCID 0000-0001-7894-6187
Vojtech KratkyDepartment of Nephrology, General University Hospital and First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Zdenka HruskovaDepartment of Nephrology, General University Hospital and First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.ORCID 0000-0002-2658-365X
Vladimir TesarDepartment of Nephrology, General University Hospital and First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.ORCID 0000-0001-6982-0689
Kai-Uwe EckardtDepartment of Nephrology and Medical Intensive Care, Charité, Berlin, Germany.ORCID 0000-0003-3823-0920
Adrian SchreiberExperimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany.ORCID 0000-0003-1244-6379
Sofia ForslundExperimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany. Sofia.Forslund@mdc-berlin.de.ORCID 0000-0003-4285-6993
Philipp MertinsCore Unit Proteomics, Berlin Institute of Health (BIH), Charité and MDC, Berlin, Germany. Philipp.Mertins@mdc-berlin.de.ORCID 0000-0002-2245-528X
Ralph KettritzExperimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC) in the Helmholtz Association and Charité, Berlin, Germany. kettritz@charite.de.ORCID 0000-0001-5821-6718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) requires intensive immunosuppressive therapy, but continued treatment beyond remission risks serious harm. Because reliable biomarkers of remission are lacking, clinicians often prolong cost-intensive and toxic therapy unnecessarily. Here, we explore the plasma proteome to identify reliable biomarkers of disease remission in patients with AAV, adjusting for patient characteristics and clinical variables. Applying a two-tiered proteomics strategy that combines global discovery with targeted validation, we identify a protein signature of remission. We then implement the resulting 7-protein panel in a targeted mass spectrometry-based assay and confirm its diagnostic performance in an independent patient cohort. The panel consistently outperforms routine markers such as C-reactive protein and ANCA titer. Our findings suggest that this 7-protein panel provides a starting point for developing a clinical tool to support decision-making, with the potential to reduce treatment-related burden, mitigate toxicity, and lower healthcare costs. More broadly, our confounder-controlled proteomics approach provides a scalable blueprint for biomarker discovery in complex inflammatory diseases.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisBiomarkersProteomeProteomicsAgedAntibodies, Antineutrophil CytoplasmicC-Reactive ProteinFemaleHumansMaleMass SpectrometryMiddle AgedRemission InductionAntibodies, Antineutrophil CytoplasmicBiomarkersC-Reactive ProteinProteome

Identifiers

PMID42481524
PMCPMC13389191

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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.