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

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: IgA class-switched CD27-CD21+ B cells in IgA nephropathy.
Συγγραφείς: 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., Slisere B; Joint Laboratory, Pauls Stradins Clinical University Hospital, Riga, Latvia.; Department of Doctoral Studies, Riga Stradins University, Riga, Latvia., 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., Kuzema V; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.; Department of Internal Diseases, Riga Stradins University, Riga, Latvia., Karklins R; Department of Internal Diseases, Riga Stradins University, Riga, Latvia., Saulite M; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.; Department of Internal Diseases, Riga Stradins University, Riga, Latvia., Seilis J; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia., Saulite AJ; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia., 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., Vaivode K; Institute of Microbiology and Virology, Riga Stradins University, Riga, Latvia., Pjanova D; Institute of Microbiology and Virology, Riga Stradins University, Riga, Latvia., Kroica J; Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia., Cernevskis H; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.; Department of Internal Diseases, Riga Stradins University, Riga, Latvia., Lejnieks A; Department of Internal Diseases, Riga Stradins University, Riga, Latvia.; Riga East Clinical University Hospital, Riga, Latvia., Petersons A; Department of Nephrology, Pauls Stradins Clinical University Hospital, Riga, Latvia.; Department of Internal Diseases, Riga Stradins University, Riga, Latvia., 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.
Πηγή: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2025 Feb 28; Vol. 40 (3), pp. 505-515.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print Cited Medium: Internet ISSN: 1460-2385 (Electronic) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE
Imprint Name(s): Publication: Oxford : Oxford University Press
Original Publication: [Berlin ; New York, NY] : Springer International, [c1986-
Ιατρικοί όροι (MeSH): Glomerulonephritis, IGA*/immunology , Glomerulonephritis, IGA*/metabolism , Glomerulonephritis, IGA*/pathology , Immunoglobulin A*/immunology , B-Lymphocytes*/immunology , B-Lymphocytes*/metabolism , Tumor Necrosis Factor Receptor Superfamily, Member 7*/metabolism , Tumor Necrosis Factor Receptor Superfamily, Member 7*/immunology , Receptors, Complement 3d*/metabolism , Receptors, Complement 3d*/immunology , Immunoglobulin Class Switching*/immunology, Humans ; Male ; Female ; Adult ; Case-Control Studies ; Middle Aged ; Prognosis ; Lymphocyte Activation ; Flow Cytometry ; Follow-Up Studies
Περίληψη: Background: Immunoglobulin 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.
Methods: We 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.
Results: In 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.
Conclusion: We 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.
(© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.)
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Grant Information: lzp-2019/1-0139 Latvian Council of Science
Contributed Indexing: Keywords: B cells; IgA nephropathy; IgA-producing plasmablasts; antibodies; disease mechanisms
Substance Nomenclature: 0 (Immunoglobulin A)
0 (Tumor Necrosis Factor Receptor Superfamily, Member 7)
0 (Receptors, Complement 3d)
Entry Date(s): Date Created: 20240717 Date Completed: 20250423 Latest Revision: 20250514
Update Code: 20260130
PubMed Central ID: PMC11879059
DOI: 10.1093/ndt/gfae173
PMID: 39020236
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1460-2385
DOI:10.1093/ndt/gfae173