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Recent progress in the pathophysiology and treatment of FSGS recurrence
Summary
Focal segmental glomerulosclerosis (FSGS) is a kidney disease causing proteinuria and often progressing to kidney failure. Current treatments for FSGS recurrence after transplant are limited, highlighting the need for new therapeutic strategies.
Area of Science:
- Nephrology
- Immunology
- Transplantation
Background:
- Focal segmental glomerulosclerosis (FSGS) is a leading cause of nephrotic syndrome and end-stage renal disease.
- FSGS recurrence post-kidney transplantation affects approximately 25% of patients, jeopardizing graft survival.
- Pathogenesis may involve T and B cell abnormalities or circulating permeability factors damaging podocytes.
Purpose of the Study:
- To review the current understanding of FSGS pathogenesis and recurrence.
- To evaluate existing and emerging treatment strategies for FSGS recurrence.
- To highlight the unmet need for effective therapies in FSGS.
Main Methods:
- Literature review of experimental and clinical studies on FSGS.
- Analysis of data on T and B cell roles in FSGS pathogenesis.
- Evaluation of treatment outcomes for plasmapheresis, cyclosporine, antiproteinuric agents, and rituximab.
Main Results:
- Current treatments like plasmapheresis and cyclosporine have limitations for FSGS recurrence.
- Antiproteinuric agents are underutilized despite evidence of slowing renal decline.
- Rituximab shows promise but requires further investigation for safety and efficacy.
Conclusions:
- FSGS recurrence remains a significant challenge in kidney transplantation.
- Novel therapeutic approaches are urgently needed to improve long-term allograft survival.
- Targeting immune pathways and optimizing proteinuria management are key areas for future research.
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