Related Experiment Video
Updated: Apr 22, 2026

Robot-Assisted Kidney Transplantation
Published on: July 19, 2021
Clinical outcomes of ABO-incompatible kidney transplant with rituximab and double-filtration plasmapheresis
Seungyeup Han1, Eunah Hwang, Sungbae Park
1From the Department of Internal Medicine and the Keimyung University Kidney Institution, Daegu, Korea.
Objectives:
The best treatment for end-stage renal disease is kidney transplant, but the shortage of donor organs has caused long waiting times for an appropriate organ allograft. The use of ABO-incompatible kidney transplant can be a valuable option to expand the donor pool. The purpose of the present study was to evaluate 13 patients who had successful ABO-incompatible kidney transplant with double-filtration plasmapheresis and rituximab.
Materials And Methods:
From January 2011 to August 2012, there were 13 patients who had ABO-incompatible kidney transplant. Antibody titers were monitored during preconditioning and after transplant. Preconditioning protocol included rituximab, mycophenolate mofetil, tacrolimus, corticosteroids, double-filtration plasmapheresis, and intravenous immunoglobulin.
Results:
There were no episodes of acute T-cell or antibody-mediated rejection. There were no surgical complications except postoperative bleeding in 1 patient. Mean serum creatinine at 2 weeks after transplant was 71 ± 18 μmol/L (0.8 ± 0.2 mg/dL). At mean follow-up 267 days (range, 1-19 mo), there was no graft loss or patient death.
Conclusions:
The ABO-incompatible kidney transplants were successful after the preconditioning protocol that included double-filtration plasmapheresis and rituximab. The use of ABO-incompatible kidney transplant may increase the availability of kidney transplant and avoid or shorten dialysis. Future multicenter studies are justified to develop a standardized preconditioning protocol.
Insights
ABO-incompatible kidney transplants using double-filtration plasmapheresis and rituximab show success. This approach expands donor availability, potentially reducing dialysis needs for end-stage renal disease patients.
Area of Science:
- Nephrology
- Transplantation Immunology
Background:
- Kidney transplantation is the optimal treatment for end-stage renal disease (ESRD).
- A significant shortage of donor organs leads to prolonged waiting times for kidney allografts.
- ABO-incompatible kidney transplantation offers a strategy to broaden the donor organ pool.
Purpose of the Study:
- To evaluate the efficacy and safety of ABO-incompatible kidney transplantation.
- To assess a preconditioning protocol involving double-filtration plasmapheresis and rituximab in 13 ESRD patients.
Main Methods:
- Retrospective analysis of 13 ABO-incompatible kidney transplant recipients from January 2011 to August 2012.
- Preconditioning regimen included rituximab, mycophenolate mofetil, tacrolimus, corticosteroids, double-filtration plasmapheresis, and intravenous immunoglobulin.
- Monitoring of antibody titers and patient outcomes, including rejection episodes, complications, and graft survival.
Main Results:
- No instances of acute T-cell or antibody-mediated rejection were observed.
- One patient experienced postoperative bleeding; otherwise, no surgical complications occurred.
- Excellent graft function was noted, with a mean serum creatinine of 71 ± 18 μmol/L at two weeks post-transplant. No graft loss or patient death occurred during a mean follow-up of 267 days.
Conclusions:
- The employed preconditioning protocol, including double-filtration plasmapheresis and rituximab, facilitated successful ABO-incompatible kidney transplantation.
- This approach can increase kidney allograft availability, potentially shortening or eliminating the need for dialysis.
- Further multicenter research is warranted to establish a standardized preconditioning protocol for ABO-incompatible kidney transplants.
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