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

B cells IgA-producing plasmablasts antibodies disease mechanisms, IgA nephropathy

Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
17 Jul 2024
Historique:
medline: 18 7 2024
pubmed: 18 7 2024
entrez: 17 7 2024
Statut: aheadofprint

Résumé

IgA nephropathy (IgAN) is characterised 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. We carried out flow cytometry analysis of peripheral blood B cells in patients with IgA nephropathy 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. In addition to global changes in the B cell landscape - expansion of naive 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 CD21pos. IgAN patients further have an expanded population of IgApos antibody-secreting cells, which correlate with serum IgA levels. Both IgApos plasmabalsts and CD27neg B cells co-express GdIgA1. Implicating dysregulation at mucosal surfaces as the driver of such B cell differentiation, we found a correlation between lipopolysaccharide (LPS) in the serum and IgAposCD27neg B cell frequency. We propose that dysregulated immunity in the mucosa may drive de novo B cell activation within germinal centres, giving rise to IgAposCD27neg B cells and subsequently IgA-producing plasmablasts. These data integrate B cells into the paradigm of IgAN pathogenesis and allow to further investigate this pathway to uncover biomarkers and develop therapeutic interventions.

Sections du résumé

BACKGROUND BACKGROUND
IgA nephropathy (IgAN) is characterised 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.
METHODS METHODS
We carried out flow cytometry analysis of peripheral blood B cells in patients with IgA nephropathy 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.
RESULTS RESULTS
In addition to global changes in the B cell landscape - expansion of naive 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 CD21pos. IgAN patients further have an expanded population of IgApos antibody-secreting cells, which correlate with serum IgA levels. Both IgApos plasmabalsts and CD27neg B cells co-express GdIgA1. Implicating dysregulation at mucosal surfaces as the driver of such B cell differentiation, we found a correlation between lipopolysaccharide (LPS) in the serum and IgAposCD27neg B cell frequency.
CONCLUSION CONCLUSIONS
We propose that dysregulated immunity in the mucosa may drive de novo B cell activation within germinal centres, giving rise to IgAposCD27neg B cells and subsequently IgA-producing plasmablasts. These data integrate B cells into the paradigm of IgAN pathogenesis and allow to further investigate this pathway to uncover biomarkers and develop therapeutic interventions.

Identifiants

pubmed: 39020236
pii: 7716060
doi: 10.1093/ndt/gfae173
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Auteurs

Anna Popova (A)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia.
Department of Internal Medicine, University of Latvia, Riga, Latvia.

Baiba Slisere (B)

Joint Laboratory, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Doctoral Studies, Riga Stradins University, Riga, Latvia.

Karlis Racenis (K)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Viktorija Kuzema (V)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Roberts Karklins (R)

Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Mikus Saulite (M)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Janis Seilis (J)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.

Anna Jana Saulite (AJ)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.

Aiga Vasilvolfa (A)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Internal Medicine, University of Latvia, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Kristine Vaivode (K)

Institute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.

Dace Pjanova (D)

Institute of Microbiology and Virology, Riga Stradins University, Riga, Latvia.

Juta Kroica (J)

Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia.

Harijs Cernevskis (H)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Aivars Lejnieks (A)

Department of Internal Diseases, Riga Stradins University, Riga, Latvia.
Riga East Clinical University Hospital, Riga, Latvia.

Aivars Petersons (A)

Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Department of Internal Diseases, Riga Stradins University, Riga, Latvia.

Kristine Oleinika (K)

Department of Internal Diseases, Riga Stradins University, Riga, Latvia.
Program in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical, School, Boston, MA, USA.

Classifications MeSH