Pierre Ronco1, Hanna Debiec. 1. INSERM Unit UMR S 702, Pierre et Marie Curie University-Paris 6, AP-HP (Tenon Hospital), Paris, France. pierre.ronco@tnn.aphp.fr
Abstract
BACKGROUND: Membranous nephropathy (MN), a major cause of nephrotic syndrome in the adult, is an immune-mediated disease characterized by the accumulation of subepithelial immune deposits leading to complement activation and podocyte injury. However, the target antigens of circulating antibodies are unknown. Current treatments for patients with MN are entirely empirical, and concept-driven therapies are dramatically lacking. METHODS: Specificity of circulating antibodies and composition of glomerular deposits were analyzed in Heymann nephritis (HN), a faithful rat model of MN, and in a subset of patients with antenatal MN. RESULTS: 20 years after the identification of megalin as the podocyte target antigen of nephritogenic antibodies in HN, we identified the human counterpart of megalin, the enzymatic podocyte antigen neutral endopeptidase (NEP). Antibodies to megalin or NEP induce formation of subepithelial immune deposits and of C5b-9, the membrane attack complex of complement. CONCLUSION: It is likely that antigens involved in idiopathic MN are expressed at the podocyte membrane. Their identification together with that of immunodominant epitopes may lead to specific antigen/ epitope-based immunotherapy aimed at inducing specific tolerance. (c) 2007 S. Karger AG, Basel.
BACKGROUND:Membranous nephropathy (MN), a major cause of nephrotic syndrome in the adult, is an immune-mediated disease characterized by the accumulation of subepithelial immune deposits leading to complement activation and podocyte injury. However, the target antigens of circulating antibodies are unknown. Current treatments for patients with MN are entirely empirical, and concept-driven therapies are dramatically lacking. METHODS: Specificity of circulating antibodies and composition of glomerular deposits were analyzed in Heymann nephritis (HN), a faithful rat model of MN, and in a subset of patients with antenatal MN. RESULTS: 20 years after the identification of megalin as the podocyte target antigen of nephritogenic antibodies in HN, we identified the human counterpart of megalin, the enzymatic podocyte antigen neutral endopeptidase (NEP). Antibodies to megalin or NEP induce formation of subepithelial immune deposits and of C5b-9, the membrane attack complex of complement. CONCLUSION: It is likely that antigens involved in idiopathic MN are expressed at the podocyte membrane. Their identification together with that of immunodominant epitopes may lead to specific antigen/ epitope-based immunotherapy aimed at inducing specific tolerance. (c) 2007 S. Karger AG, Basel.
Authors: Daniel Smyk; Tassos Grammatikopoulos; Alexandros Daponte; Eirini I Rigopoulou; Dimitrios P Bogdanos Journal: Auto Immun Highlights Date: 2011-03-23
Authors: Barbara Lewko; Anna Waszkiewicz; Anna Maryn; Magdalena Gołos; Elżbieta Latawiec; Agnieszka Daca; Jacek M Witkowski; Stefan Angielski; Jan Stępiński Journal: Mol Cell Biochem Date: 2015-08-14 Impact factor: 3.396
Authors: Juliana Reis Machado; Laura Penna Rocha; Precil Diego Miranda de Menezes Neves; Eliângela de Castro Cobô; Marcos Vinícius Silva; Lúcio Roberto Castellano; Rosana Rosa Miranda Corrêa; Marlene Antônia Reis Journal: Int J Nephrol Date: 2012-07-11