Evidence map›Paper›PMID 39939347›Full record

ArticleNature communications2025

Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis.

C M Wortel, R van de Wetering, E M Stork, T Kissel, S Reijm, D van der Woude, K A van Schie, L A Trouw, Yko Teng, A Rutgers and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
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

16 authors.

C M Wortel *Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-3583-6281
R van de Wetering *Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-5330-5113
E M StorkDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9629-8950
T KisselDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-5749-8087
S ReijmDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-4424-4256
D van der WoudeDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-8121-5879
K A van SchieDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9703-2441
L A TrouwDepartment of Immunology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-5186-2290
Yko TengDepartment of Nephrology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0001-9920-2195
A RutgersDepartment of Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, The Netherlands.
P HeeringaDepartment of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0001-8684-763X
R E VollDepartment of Rheumatology and Clinical Immunology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-5542-9133
M RizziDepartment of Rheumatology and Clinical Immunology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-5153-6089
Rem ToesDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-9618-6414
H U SchererDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands. h.u.scherer@lumc.nl.ORCID http://orcid.org/0000-0002-5700-5617

Funding

Reumafonds (Dutch Arthritis Foundation) 15-2-402 and 18-1-205
6 · The paper itself

Abstract

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a prototypic autoimmune disease, with a subset of AAV patients manifesting anti-myeloperoxidase (MPO) IgG. Patients with AAV respond positively to B cell-targeting and complement-targeting therapies, but disease flares are not uncommon. Here, by comparing samples from healthy individuals and MPO

Indexed as

Antibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisB-LymphocytesImmunoglobulin MPeroxidaseAdultAgedComplement ActivationFemaleHumansImmunoglobulin GMaleMiddle AgedAntibodies, Antineutrophil CytoplasmicImmunoglobulin GImmunoglobulin MMPO protein, humanPeroxidase

Identifiers

PMID39939347
PMCPMC11822119

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.