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Rituximab for post-transplant recurrences of FSGS
Umut Selda Bayrakci1, Esra Baskin, Hale Sakalli
1Department of Pediatric Nephrology, Baskent University Faculty of Medicine, Ankara, Turkey.
Insights
Rituximab effectively treated severe post-transplant proteinuria recurrence in a young FSGS patient. This B-cell depleting therapy achieved remission, demonstrating its potential for managing Focal Segmental Glomerulosclerosis (FSGS) recurrence after kidney transplantation.
Area of Science:
- Nephrology
- Immunology
- Transplantation
Background:
- Focal Segmental Glomerulosclerosis (FSGS) is a leading cause of nephrotic syndrome in children and adults.
- Recurrence of FSGS post-kidney transplantation is a significant clinical challenge, often leading to graft dysfunction.
- Standard immunosuppressive therapies can be insufficient in preventing or treating FSGS recurrence.
Observation:
- A 14-year-old boy with primary FSGS experienced severe proteinuria immediately after a second living-related kidney transplant.
- Despite conventional immunosuppression (steroids, cyclosporine A, daclizumab, mycophenolate mofetil), proteinuria and serum creatinine levels worsened.
- Rituximab was administered on post-transplant day four.
Findings:
- Four weekly doses of rituximab (375 mg/m(2)/dose) led to rapid depletion of circulating CD19-positive B cells.
- Remission of proteinuria was achieved six weeks after initiating rituximab treatment.
- Excellent graft function was maintained six months post-transplantation, with minimal proteinuria.
Implications:
- Rituximab represents a promising therapeutic option for managing post-transplant FSGS recurrence.
- Targeting B cells with rituximab may offer a more effective strategy than conventional immunosuppression in select cases.
- This case highlights the potential of novel immunotherapies in improving outcomes for kidney transplant recipients with recurrent FSGS.
Abstract:
A 14-yr-old boy whose primary kidney disease was FSGS developed severe recurrence of proteinuria immediately after a second living-related kidney transplant. Despite pre- and post-operative PP and immunosuppressive treatment consisting of steroids, CycA, daclizumab, and MMF, daily protein excretion and serum creatinine increased. We therefore administered rituximab on the fourth day of transplantation. He received four weekly doses of rituximab (375 mg/m(2)/dose), which resulted in a rapid clearing of circulating CD19-positive B cells, and remission of proteinuria was achieved six wk after the first rituximab treatment. Graft function was excellent six months after transplantation with proteinuria of 8 mg/m(2)/h. We conclude that rituximab may be an effective treatment for post-transplant recurrence of FSGS.
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