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Updated: Apr 16, 2026

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
Optimizing HLA matching in a highly sensitized pediatric patient using ABO-incompatible and paired exchange kidney
Anjali B Nayak1, Robert B Ettenger, Suzanne McGuire
1Department of Pediatrics, OU Childrens, University of Oklahoma Health Sciences Center, 1200 N Children's Avenue, Suite 14200, Oklahoma City, OK, 73104, USA, anjali-nayak@ouhsc.edu.
Insights
Pediatric kidney transplants can be optimized using ABO-incompatible (ABOi) paired exchange programs. This strategy enhances human leukocyte antigen (HLA) matching, reduces wait times, and improves long-term graft survival in children.
Area of Science:
- Pediatric Nephrology
- Transplantation Immunology
- Organ Transplantation
Background:
- Kidney transplantation is optimal for end-stage renal disease, especially in pediatric patients requiring long-term graft survival.
- Minimizing long-term sensitization through well-matched transplants is crucial for pediatric recipients.
- Limited availability of well-matched deceased donor organs challenges timely pediatric kidney transplantation.
Observation:
- A highly sensitized pediatric patient (cPRA 90%) underwent a successful ABO-incompatible (ABOi) paired exchange kidney transplant.
- The patient received pre-transplant immunomodulation to achieve an isohemagglutinin titer <1:8.
- Immunosuppression included anti-thymocyte globulin induction and triple therapy with steroids.
Findings:
- Excellent 18-month allograft function with an eGFR of 83.53 ml/min/1.73 m(2).
- Absence of de novo donor-specific HLA antibodies.
- No episodes of acute rejection were observed.
Implications:
- Paired exchange combined with ABOi kidney transplants is a safe and effective strategy for pediatric recipients.
- This approach optimizes HLA matching and reduces wait times for pediatric kidney transplants.
- Utilizing ABOi paired exchange enhances living donor kidney transplantation and improves allograft survival in children.
Background:
Kidney transplantation is the treatment of choice for end-stage renal disease. However, since pediatric patients have long projected life-years, it is also optimal for them to get well-matched transplants to minimize long-term sensitization. In North America, pediatric kidney transplantation is largely dependent upon the use of deceased donor organs, making it challenging to identify timely, well-matched transplants. Pediatric recipients may have willing living donors who are either HLA- or ABO-incompatible (ABOi); therefore, one solution is to utilize ABOi transplants and paired exchange programs to enhance HLA matching and living donation.
Case-Diagnosis/Treatment:
We adopted this approach for a highly sensitized patient with cPRA 90%, who received a successful ABOi paired exchange transplant. The recipient received pre-transplant immunomodulation until an acceptable isohemagglutinin titer <1:8 was reached before transplantation. The patient was induced with anti-thymocyte globulin and maintained on steroid-based triple immunosuppression. Eighteen-month allograft function is excellent with an estimated glomerular filtration rate (eGFR) of 83.53 ml/min/1.73 m(2). The patient did not develop de novo donor-specific HLA antibodies or have any episodes of acute rejection
Conclusions:
This case highlights the safety and efficacy of using paired exchange in combination with ABOi transplants in pediatric kidney transplantation to optimize HLA matching, minimize wait times, and enhance allograft survival.
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