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Relapse of membranous glomerulopathy after kidney transplantation: sustained remittance induced by rituximab
H Weclawiak1, D Ribes, C Guilbeau-Frugier
1Department of Nephrology, Dialysis and Multiorgan Transplantation, CHU Rangueil, Toulouse, France.
Abstract:
Membranous glomerulopathy (MG) is a rare cause of chronic kidney disease. However, after kidney transplantation (KT), despite immunosuppression, it often relapses on the allograft. Herein, we report on a male kidney-transplant patient, aged 27 years, who developed overt nephrotic syndrome 11 months after KT. This was related to relapsing MG, as evidenced by the allograft biopsy, which, in addition, showed CD3 (+) and CD20 (+) interstitial lymphocyte infiltration. The patient was treated with rituximab: 375 mg/m2/week for 4 consecutive weeks, followed by one additional injection every 3 months for one year. Remission was observed before the third rituximab injection. After a follow-up of 42 months, the patient was still in remission, i.e., microalbuminuria of 107 mg/day.
Insights
Membranous glomerulopathy (MG) often relapses after kidney transplantation (KT). Rituximab treatment led to sustained remission in a young male patient with relapsing MG post-transplant.
Area of Science:
- Nephrology
- Transplantation Immunology
Background:
- Membranous glomerulopathy (MG) is a leading cause of nephrotic syndrome in adults.
- MG frequently recurs in kidney allografts despite standard immunosuppression.
- Recurrence poses a significant threat to long-term graft survival.
Observation:
- A 27-year-old male kidney transplant recipient developed nephrotic syndrome 11 months post-transplant.
- Allograft biopsy confirmed recurrent membranous glomerulopathy with significant lymphocyte infiltration.
- The patient presented with overt nephrotic syndrome and declining graft function.
Findings:
- Treatment with rituximab induced clinical remission of nephrotic syndrome.
- Remission was achieved before the third maintenance dose of rituximab.
- Sustained remission, indicated by low-level proteinuria, was maintained for 42 months post-treatment.
Implications:
- Rituximab may be an effective therapeutic option for relapsing membranous glomerulopathy in kidney transplant recipients.
- Targeting B-cells with rituximab could offer a novel strategy for managing antibody-mediated kidney diseases post-transplantation.
- This case highlights the potential for successful treatment of challenging allograft complications.
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