Evidence map›Paper›PMID 39020236›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2025

IgA class-switched CD27-CD21+ B cells in IgA nephropathy.

Anna Popova, Baiba Slisere, Karlis Racenis, Viktorija Kuzema, Roberts Karklins, Mikus Saulite, Janis Seilis, Anna Jana Saulite, Aiga Vasilvolfa, Kristine Vaivode and 6 more

Abstract read
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. The Roles of A Proliferation-Inducing Ligand (APRIL) and B-Cell Activating Factor (BAFF) in IgA Nephropathy.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
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.

Anna PopovaDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0002-3916-4040
Baiba SlisereJoint Laboratory, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0002-6129-0983
Karlis RacenisDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0001-7123-4048
Viktorija KuzemaDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0002-3120-8096
Roberts KarklinsDepartment of Internal Diseases, Riga Stradins University, Riga, Latvia.ORCID 0009-0004-3501-9059
Mikus SauliteDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0001-5383-0129
Janis SeilisDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Anna Jana SauliteDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Aiga VasilvolfaDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Kristine VaivodeInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Dace PjanovaInstitute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.
Juta KroicaDepartment of Biology and Microbiology, Riga Stradins University, Riga, Latvia.ORCID 0000-0003-0805-7063
Harijs CernevskisDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0002-3797-1041
Aivars LejnieksDepartment of Internal Diseases, Riga Stradins University, Riga, Latvia.ORCID 0000-0002-2097-6698
Aivars PetersonsDepartment of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.ORCID 0000-0001-8109-1968
Kristine OleinikaDepartment of Internal Diseases, Riga Stradins University, Riga, Latvia.ORCID 0000-0002-2021-2938

Funding

Latvian Council of Science lzp-2019/1-0139
6 · The paper itself

Abstract

backgroundImmunoglobulin A nephropathy (IgAN) is characterized by the production of galactose-deficient IgA1 (GdIgA1) antibodies. As the source of pathogenic antibodies, B cells are central to IgAN pathogenesis, but the B cell activation pathways as well as the potential B cell source of dysregulated IgA secretion remain unknown.

methodsWe carried out flow cytometry analysis of peripheral blood B cells in patients with IgAN and control subjects with a focus on IgA-expressing B cells to uncover the pathways of B cell activation in IgAN and how these could give rise to pathogenic GdIgA1 antibodies.

resultsIn addition to global changes in the B cell landscape-expansion of naïve and reduction in memory B cells-IgAN patients present with an increased frequency of IgA-expressing B cells that lack the classical memory marker CD27, but are CD21+. IgAN patients furthermore have an expanded population of IgA+ antibody-secreting cells, which correlate with serum IgA levels. Both IgA+ plasmabalsts and CD27- B cells co-express GdIgA1. Implicating dysregulation at mucosal surfaces as the driver of such B cell differentiation, we found a correlation between lipopolysaccharide in the serum and IgA+CD27- B cell frequency.

conclusionWe propose that dysregulated immunity in the mucosa may drive de novo B cell activation within germinal centres, giving rise to IgA+CD27- B cells and subsequently IgA-producing plasmablasts. These data integrate B cells into the paradigm of IgAN pathogenesis and allow further investigation of this pathway to uncover biomarkers and develop therapeutic interventions.

Indexed as

B-LymphocytesGlomerulonephritis, IGAImmunoglobulin AImmunoglobulin Class SwitchingReceptors, Complement 3dTumor Necrosis Factor Receptor Superfamily, Member 7AdultCase-Control StudiesFemaleFlow CytometryFollow-Up StudiesHumansLymphocyte ActivationMaleMiddle AgedPrognosisImmunoglobulin AReceptors, Complement 3dTumor Necrosis Factor Receptor Superfamily, Member 7antibodiesB cellsdisease mechanismsIgA nephropathyIgA-producing plasmablasts

Identifiers

PMID39020236
PMCPMC11879059

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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.