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Updated: Sep 2, 2025

Robot-Assisted Kidney Transplantation
Published on: July 19, 2021
Experiences of performing ABO-incompatible kidney transplantation in Bangladesh
Nura Afza Salma Begum1, Tasnuva Sarah Kashem1, Farnaz Nobi1
1Department of Nephrology, Kidney Foundation Hospital and Research Institute, Dhaka, Bangladesh.
Insights
ABO-incompatible kidney transplants (ABOi KT) in Bangladesh offer hope for end-stage renal disease patients. While successful, managing infection and rejection risks is crucial for expanding this life-saving procedure.
Area of Science:
- Nephrology
- Transplantation Immunology
- Surgical Innovation
Background:
- Rising end-stage renal disease (ESRD) in Bangladesh necessitates expanded transplantation options.
- Living kidney donation is primary but limited by ABO compatibility.
- ABO-incompatible kidney transplantation (ABOi KT) has been performed since 2018.
Purpose of the Study:
- To examine the experiences and outcomes of ABOi KT in Bangladesh.
- To assess the feasibility and challenges of ABOi KT in a resource-limited setting.
Main Methods:
- A desensitization protocol involving rituximab, plasma exchange (PEX), and intravenous immunoglobulin was used.
- Immunosuppression included tacrolimus, mycophenolate mofetil, and prednisolone, with basiliximab induction.
- Transplantation was performed at anti-ABO antibody titers ≤18 after 3-5 PEX sessions.
Main Results:
- 100% graft survival was observed in seven ABOi KT cases over a mean of 22 months.
- Two patients experienced acute rejection, successfully treated with methylprednisolone.
- Infection, including cytomegalovirus pneumonia, was the most common complication, leading to two deaths with functioning grafts.
Conclusions:
- ABOi KT significantly expands the donor pool for ESRD patients in Bangladesh.
- High costs and risks of rejection and infection are major challenges.
- Further research and optimized protocols are needed to improve outcomes and accessibility.
Background:
The number of end-stage renal disease (ESRD) patients is increasing in Bangladesh. Currently, living kidney donation is the only viable option for transplantation in Bangladesh, and it is further restricted by ABO compatibility issues. We have performed ABO-incompatible kidney transplantations (ABOi KTs) in Bangladesh since 2018. This study examines our experiences with seven cases of ABOi KT.
Methods:
The desensitization protocol included low-dose rituximab (100 mg/body) followed by plasma exchange (PEX), which was followed by a 5-g dose of intravenous immunoglobulin. Immunosuppression was undertaken using tacrolimus (0.1 mg/kg/day), mycophenolate mofetil (1,500 mg/day), and prednisolone (0.5 mg/kg/day). All patients received basiliximab for induction therapy.
Results:
The median baseline anti-ABO antibody titer was 164 (range, 132-1128). Transplantation was performed at a titer of ≤18. Our patients attended three to five PEX sessions before transplantation. Graft survival was 100% in the seven cases over a mean period of 22 months. The mean creatinine level was 204.6±47.4 µmol/L. Two patients were suspected of having developed acute rejection and received intravenous methylprednisolone, resulting in improved kidney function. One patient required posttransplant hemodialysis due to delayed graft function and subsequently improved. Infection was the most common complication experienced by ABOi KT patients. Two patients developed severe cytomegalovirus pneumonia and died with functioning grafts.
Conclusions:
ABOi KT in Bangladesh will substantially expand the living kidney donor pool and bring hope to a large number of ESRD patients without ABO-compatible donors. However, the high cost and risk of acute rejection and infection remain major concerns.
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