Angiotensin II Type 2 Receptor Antibodies in Glomerular Diseases.


Journal

Archivum immunologiae et therapiae experimentalis
ISSN: 1661-4917
Titre abrégé: Arch Immunol Ther Exp (Warsz)
Pays: Poland
ID NLM: 0114365

Informations de publication

Date de publication:
01 Jan 2024
Historique:
received: 24 01 2024
accepted: 24 06 2024
medline: 21 8 2024
pubmed: 21 8 2024
entrez: 21 8 2024
Statut: epublish

Résumé

We evaluated the concentration of AT2R antibodies in 136 patients with primary and secondary glomerular diseases: membranous nephropathy (n = 18), focal and segmental glomerulosclerosis (n = 25), systemic lupus erythematosus (n = 17), immunoglobulin A (IgA) nephropathy (n = 14), mesangial (non-IgA) proliferative nephropathy (n = 6), c-ANCA vasculitis (n = 40), perinuclear anti-neutrophil cytoplasmic antibodies (p-ANCA) vasculitis (n = 16), and compared it with a healthy control group (22 patients). Serum creatinine levels, proteinuria, serum albumin, and total protein concentrations were prospectively recorded for 2 years. The mean levels of AT2R antibodies in the lupus nephropathy group were significantly higher compared to the control group, 64.12 ± 26.95 units/mL and 9.72 ± 11.88 units/mL, respectively. There was no association between this level and the clinical course of the disease. The AT2R levels in other kinds of glomerular disease were no different from the control group. We found significant correlations between AT1R and AT2R in patients with membranous nephropathy (r = 0.66), IgA nephropathy (r = 0.61), and c-ANCA vasculitis (r = 0.63). Levels of AT2R antibodies in systemic lupus erythematosus are higher compared to other types of glomerulonephritis, vasculitis, and a healthy control group. Levels of AT2R antibodies correlate with AT1R antibodies in the groups of patients with membranous nephropathy, IgA nephropathy, and c-ANCA vasculitis. These kinds of AT2R antibodies have a stimulative effect on AT2R, but we have not found the influence of these antibodies on the clinical course of glomerular diseases.

Identifiants

pubmed: 39166802
pii: aite-2024-0017
doi: 10.2478/aite-2024-0017
doi:

Substances chimiques

Receptor, Angiotensin, Type 2 0
Autoantibodies 0
Antibodies, Antineutrophil Cytoplasmic 0
Receptor, Angiotensin, Type 1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 Maciej Szymczak et al., published by Sciendo.

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Auteurs

Maciej Szymczak (M)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Harald Heidecke (H)

2CellTrend Gmbh, Luckenwalde, Germany.

Marcelina Żabińska (M)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Dagna Rukasz (D)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Krzysztof Wiśnicki (K)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Krzysztof Kujawa (K)

3Statistical Analysis Centre, Wroclaw Medical University, Wroclaw, Poland.

Katarzyna Kościelska-Kasprzak (K)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Magdalena Krajewska (M)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

Mirosław Banasik (M)

1Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

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