Evidence map›Paper›PMID 39420623›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2025

Evidence of Site-Specific Mucosal Autoantibody Secretion in Rheumatoid Arthritis.

Veerle F A M Derksen, Klara Martinsson, Anouk G van Mourik, Carlijn A Wagenaar, René E M Toes, Wendy Walrabenstein, Daniel Sjöberg, Dirkjan van Schaardenburg, Tom W J Huizinga, Alf Kastbom and 2 more

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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

12 authors.

Veerle F A M DerksenLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-8246-7055
Klara MartinssonLinköping University, Linköping, Sweden.ORCID 0000-0003-4492-9172
Anouk G van MourikLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-3811-7373
Carlijn A WagenaarReade and Amsterdam University Medical Center, Amsterdam, The Netherlands.
René E M ToesLeiden University Medical Center, Leiden, The Netherlands.
Wendy WalrabensteinAmsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.ORCID 0000-0002-2428-2845
Daniel SjöbergUppsala University, Uppsala, Sweden, and Falun Hospital, Falun, Sweden.
Dirkjan van SchaardenburgReade and Amsterdam University Medical Center, Amsterdam, The Netherlands.
Tom W J HuizingaLeiden University Medical Center, Leiden, The Netherlands.
Alf KastbomLinköping University, Linköping, Sweden.ORCID 0000-0001-7187-1477
Anna SvärdLinköping University, Linköping, Sweden, and Uppsala University, Uppsala, Sweden.
Diane van der WoudeLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-8121-5879

Funding

Center for Clinical Research DalarnaDutch Research CouncilNetherlands Organization for Health Research and DevelopmentReade FoundationStichting Vermeer 14Uppsala UniversityW. M. de Hoop StichtingW.M. de Hoop Stichting
6 · The paper itself

Abstract

objectiveAnti-citrullinated protein antibodies (ACPA) have been detected in sputum and saliva, indicating that anti-modified protein antibodies (AMPA) can be produced at mucosal sites in patients with rheumatoid arthritis (RA). However, the body's largest mucosal compartment, the gut, has not yet been examined. We therefore investigated the presence of several AMPA (ACPA, anti-carbamylated protein antibodies [anti-CarP], and anti-acetylated protein antibodies [AAPA]) at different mucosal sites, including the intestinal tract.

methodsPaired fecal/ileal wash, saliva, and serum samples of patients with RA and healthy volunteers were collected in two independent cohorts. Data involving feces were replicated in a third cohort. In these secretions, AMPA were analyzed using in-house enzyme-linked immunosorbent assay with unmodified peptides as control. In fecal samples, total IgA and anti-Escherichia coli IgA were measured.

resultsACPA, anti-CarP, and AAPA IgA were measurable in saliva of seropositive patients with RA (prevalence 9%-40%). No AMPA could be detected in feces. IgA was present because total IgA and anti-E. coli IgA were detectable in feces of ACPA-positive patients with RA and healthy donors. Results were confirmed in another cohort using colonoscopically collected ileal wash samples.

conclusionOur study shows the presence of ACPA, anti-CarP, and AAPA IgA in saliva of ACPA-seropositive patients with RA. However, no AMPA could be detected in feces/ileal wash samples of these patients, although our assays were able to measure other antigen-specific antibodies. These data suggest that mucosal autoantibody secretion may occur in the oral mucosa of patients with RA, whereas no evidence could be found for this process in the lower gastrointestinal tract.

Indexed as

Anti-Citrullinated Protein AntibodiesArthritis, RheumatoidAutoantibodiesIntestinal MucosaAdultAgedCase-Control StudiesFecesFemaleHumansIleumImmunoglobulin AMaleMiddle AgedSalivaAnti-Citrullinated Protein AntibodiesAutoantibodiesImmunoglobulin A

Identifiers

PMID39420623
PMCPMC11865693

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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.