Complement Activation and Effector Pathways in Membranous Nephropathy.
Complement
glomerulonephritis
glomerulus
membranous nephropathy
proteinuria
Journal
Kidney international
ISSN: 1523-1755
Titre abrégé: Kidney Int
Pays: United States
ID NLM: 0323470
Informations de publication
Date de publication:
21 Dec 2023
21 Dec 2023
Historique:
received:
01
08
2023
revised:
25
09
2023
accepted:
05
10
2023
medline:
24
12
2023
pubmed:
24
12
2023
entrez:
23
12
2023
Statut:
aheadofprint
Résumé
Complement activation has long been recognized as a central feature of membranous nephropathy. Evidence for its role has been derived from the detection of complement products in biopsy tissue and urine from membranous nephropathy patients and from mechanistic studies primarily based on the passive Heymann nephritis model. Only recently, more detailed insights into the exact mechanisms of complement activation and effector pathways have been gained from patient data, animal models and in vitro models based on specific target antigens relevant to the human disease. These data are of clinical relevance, as they parallel the recent development of numerous specific complement therapeutics for clinical use. Despite efficient B cell depletion, many patients with membranous nephropathy achieve only partial remission of proteinuria, which may be explained by the persistence of subepithelial immune complexes and ongoing complement-mediated podocyte injury. Targeting complement therefore represents an attractive adjunct treatment for membranous nephropathy, but it will need to be tailored to the specific complement pathways relevant to membranous nephropathy. This review summarizes the different lines of evidence for a central role of complement in membranous nephropathy and for the relevance of distinct complement activation and effector pathways, with a focus on recent developments.
Identifiants
pubmed: 38142037
pii: S0085-2538(23)00868-2
doi: 10.1016/j.kint.2023.10.035
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2023. Published by Elsevier Inc.