Evidence map›Paper›PMID 42343982›Full record

ArticleTH open : companion journal to thrombosis and haemostasis2026

Cross-Reactivity of Antiphospholipid Antibodies with Gut Commensal Proteins in Antiphospholipid Syndrome.

Dagmar J M van Mourik, Manon Balvers, Valérie L B I Jansen, Patrick A de Jonge, Michiel Coppens, Max Nieuwdorp, Saskia Middeldorp, Jeroen C J Eikenboom, Jan Voorberg, Thijs E van Mens

Abstract read
In one paragraph

Article in TH open : companion journal to thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Dagmar J M van MourikDivision of Thrombosis and HemostasisDepartment of Internal MedicineLeiden University Medical CenterLeidenSouth Hollandthe Netherlands.ORCID 0000-0001-9185-8974
Manon BalversDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Valérie L B I JansenDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Patrick A de JongeDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Michiel CoppensDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Max NieuwdorpDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Saskia MiddeldorpDepartment of Internal MedicineRadboud University Medical CenterNijmegenGelderlandthe Netherlands.
Jeroen C J EikenboomDivision of Thrombosis and HemostasisDepartment of Internal MedicineLeiden University Medical CenterLeidenSouth Hollandthe Netherlands.
Jan VoorbergDepartment of Vascular MedicineAmsterdam UMC, Location University of AmsterdamAmsterdamNorth Hollandthe Netherlands.
Thijs E van MensDivision of Thrombosis and HemostasisDepartment of Internal MedicineLeiden University Medical CenterLeidenSouth Hollandthe Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the persistent presence of antiphospholipid antibodies (aPL), mainly targeted against β2 glycoprotein 1 (β2GP1). The autoimmune response to β2GP1 is aimed at several B-cell and T-cell epitopes. Molecular mimicry of these epitopes by gut commensal proteins, so-called mimotopes, causing cross-immunization, might contribute to the formation of aPL. Objective: To study the potential role of gut microbiome cross-immunization in APS by examining cross-reactivity of aPL with gut commensal mimotope-containing proteins. Methods: Fecal microbial metagenome of APS patients was determined using shotgun sequencing. An in-house developed in silico pipeline was used to identify gut commensal proteins that show sequence homology with known β2GP1 B and T cell epitopes in the metagenomic data. An enzyme-linked immunosorbent assay was used to test the identified microbial proteins for IgG cross-reactivity, with plasma of 21 APS patients and 17 control participants. Results: The in silico pipeline resulted in the identification of six gut commensals with a B cell and T cell β2GP1 epitope homologue. Of these, YjjG family noncanonical pyrimidine nucleotidase, one of the candidate-β2GP1 B cell mimicking proteins, showed significantly increased IgG reactivity in APS patients compared to control participants, as well as higher binding of a specific anti-β2GP1 monoclonal antibody than a negative control. Conclusion: Our study shows reactivity of IgG antibodies to YjjG family noncanonical pyrimidine nucleotidase from

Indexed as

antiphospholipid syndromeautoimmune diseasescross-reactivityintestinal microbiomemolecular mimicry

Identifiers

PMID42343982
PMCPMC13289573

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