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Published on: May 7, 2019
De novo glomerulonephritis in renal allografts with hepatitis C virus infection
B H Ozdemir1, F N Ozdemir, S Sezer
1Department of Pathology, Baskent University, Faculty of Medicine, Ankara, Turkey. handan27@hotmail.com
Insights
Hepatitis C virus (HCV) infection significantly increases the risk of developing de novo glomerulonephritis (GN) after transplantation. HCV-positive patients with de novo GN experienced reduced graft survival, highlighting the need for vigilant monitoring.
Area of Science:
- Nephrology
- Virology
- Transplant Medicine
Background:
- Hepatitis C virus (HCV) infection is a significant concern in organ transplantation.
- Posttransplant de novo glomerulonephritis (GN) can impact graft outcomes.
Purpose of the Study:
- To investigate the influence of HCV infection on the development of de novo GN in renal transplant recipients.
- To compare the incidence and outcomes of de novo GN in HCV-positive versus HCV-negative patients.
Main Methods:
- Retrospective analysis of 165 renal transplant recipients (44 HCV-positive, 121 HCV-negative).
- Review of kidney biopsies (light and immunofluorescence microscopy) and clinical data.
- Statistical comparison of de novo GN incidence, graft survival, and disease recurrence rates.
Main Results:
- HCV-positive patients had a significantly higher incidence of de novo GN (34%) compared to HCV-negative patients (6.6%).
- De novo GN in HCV-positive recipients was associated with impaired graft survival.
- Recurrence of primary kidney diseases was more frequent in HCV-negative patients.
Conclusions:
- HCV infection is a major risk factor for developing de novo GN post-transplantation.
- Close monitoring with renal biopsies is crucial for HCV-positive transplant recipients, even without overt clinical signs.
- Understanding these associations aids in optimizing transplant management and patient outcomes.
Abstract:
The purpose of this study was to examine the influence of hepatitis C virus (HCV) infection on the occurrence of posttransplant de novo glomerulonephritis (GN). Of 165 patients selected for the study, 44 were HCV positive and 121 HCV negative. Light and immunofluorescence microscopy were performed on all biopsies and clinical and laboratory findings reviewed. Fifteen (34%) of the 44 HCV positive patients showed de novo GN (4 membranous, 11 membranoproliferative) at a mean of 47 +/- 22 months. But only 8 (6.6%) of 121 HCV negative patients showed de novo GN (5 anti-glomerular basement membrane nephritis in recipients with Alport's disease, 2 membranous GN, 1 membranoproliferative GN) at a mean of 60 +/- 39 months. The risk of development of de novo GN was higher among patients with HCV infection (P < .001). The presence of de novo GN in HCV positive patients impaired graft survival compared with HCV positive patients without de novo GN (P < .01). The incidence of recurrence of primary disease, mainly focal segmental glomerulosclerosis, membranous glomerulonephritis, membranoproliferative glomerulonephritis, and IgA nephropathy, was higher in HCV negative patients (29%) compared with HCV positive patients (6.8%; P = .001), namely, 50%, 57.6%, 25%, and 69%, respectively. In conclusion, HCV infection showed a strong influence on the development of de novo GN. For this reason, it is important to follow HCV positive recipients with a renal biopsy even when there are no significant clinical or laboratory findings.
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