» Articles » PMID: 21030574

Posttransplant Recurrence of Primary Glomerulonephritis

Overview
Specialty Nephrology
Date 2010 Oct 30
PMID 21030574
Citations 72
Authors
Affiliations
Soon will be listed here.
Abstract

All forms of primary GN may recur after kidney transplantation and potentially jeopardize the survival of the graft. IgA nephritis (IgAN) may recur in approximately one third of patients, more frequently in younger patients and in those with a rapid progression of the original disease. However, with the exception of few patients with rapid progression, there is no evidence that recurrence of IgAN has a deleterious effect on graft survival at least up to 10 years. Recurrence of focal segmental glomerulosclerosis (FSGS) is often associated with nephrotic proteinuria and is more frequent in children, in patients with rapid progression of the original disease, and in those who lost a previous transplant from recurrence. The natural course of recurrent FSGS is usually unfavorable. Early and intensive plasmapheresis may obtain complete or partial response in several patients. Good results have also been reported with rituximab. Idiopathic membranous nephropathy (IMN) may recur in 30% to 40% of patients. The graft survival in patients with IMN is not different than that of patients with other renal diseases. Good results with rituximab have been reported. Membranoproliferative GN (MPGN) may recur in 27% to 65% of patients. The recurrence is more frequent and the prognosis is more severe in type II MPGN. Although recurrent GN is relatively frequent and may worsen the outcome of renal allografts in some patients, its effect is diluted by several other risk-factors that may have a greater effect than recurrent GN on the long-term graft survival.

Citing Articles

Gene prediction of the causal relationship between immune cells and IgA nephropathy: A bidirectional Mendelian randomization study.

Zhang Y, Zhang C, Liu G, He P, Wan B Medicine (Baltimore). 2024; 103(46):e40480.

PMID: 39560595 PMC: 11575961. DOI: 10.1097/MD.0000000000040480.


Humoral immune responses primed by the alteration of gut microbiota were associated with galactose-deficient IgA1 production in IgA nephropathy.

Gao L, Li H, Liu X, Li H, Li P, Lu W Front Immunol. 2024; 15:1415026.

PMID: 39104521 PMC: 11298704. DOI: 10.3389/fimmu.2024.1415026.


Updates on C3 Glomerulopathy in Kidney Transplantation: Pathogenesis and Treatment Options.

Bartoli G, Dello Strologo A, Grandaliano G, Pesce F Int J Mol Sci. 2024; 25(12).

PMID: 38928213 PMC: 11204074. DOI: 10.3390/ijms25126508.


Recurrence of Idiopathic Membranous Nephropathy in the Kidney Allograft: A Systematic Review.

Panagakis A, Bellos I, Grigorakos K, Panagoutsos S, Passadakis P, Marinaki S Biomedicines. 2024; 12(4).

PMID: 38672095 PMC: 11048506. DOI: 10.3390/biomedicines12040739.


Risk factors and outcomes of IgA nephropathy recurrence after kidney transplantation: a systematic review and meta-analysis.

Li Y, Tang Y, Lin T, Song T Front Immunol. 2023; 14:1277017.

PMID: 38090563 PMC: 10713786. DOI: 10.3389/fimmu.2023.1277017.