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Published on: April 12, 2021
Management of sensitized pediatric patients prior to renal transplantation
Kwanchai Pirojsakul1,2,3, Dev Desai1,3, Chantale Lacelle3
1Children's Medical Center, Dallas, TX, USA.
Insights
Four highly sensitized children received desensitization therapy before kidney transplants, showing successful outcomes with low immediate rejection risk. Long-term allograft function and immunosuppression complications were encouraging.
Area of Science:
- Pediatric Nephrology
- Transplantation Immunology
- Immunosuppression Therapy
Background:
- Limited data exists on renal allograft outcomes in sensitized children.
- This study reports on four pediatric patients undergoing desensitization before kidney transplantation.
Observation:
- Four pediatric patients with end-stage renal disease received desensitization therapy due to high antibody levels or positive crossmatches.
- Treatment involved rituximab, IVIG, bortezomib, and induction therapies like plasmapheresis or alemtuzumab.
- Post-transplant immunosuppression included tacrolimus, mycophenolate mofetil, and prednisolone.
Findings:
- Donor-specific antibodies (DSA) were detected in three patients post-transplant.
- Two patients showed no rejection at one month; one later developed chronic active antibody-mediated rejection.
- One patient had transient borderline acute cellular rejection, with DSA resolving spontaneously and stable function at three years.
- Allograft function, measured by estimated glomerular filtration rate (eGFR), ranged from 30-75 mL/min/1.73 m² at 1-4.5 years post-transplant.
Implications:
- Desensitization therapy can lead to successful renal transplantation in highly sensitized pediatric patients.
- The study suggests a low risk of immediate post-transplant rejection and encouraging long-term allograft function.
- Further research is needed to assess long-term complications of immunosuppression in this population.
Background:
Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution.
Methods:
Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney disease received desensitization therapy due to: (1) positive donor-specific antibodies (DSA) and/or crossmatches with potential living donors, (2) more than three positive crossmatches with deceased donors or (3) high calculated panel-reactive antibody of >80 %. Desensitization with rituximab, intravenous immunoglobulin and bortezomib was performed in all patients. Induction therapy included combinations of plasmapheresis and/or alemtuzumab or anti-thymocyte globulin. Standard post-transplant medications included tacrolimus, mycophenolate mofetil and prednisolone.
Results:
Post-transplant screening revealed DSA in three patients. Biopsy showed no evidence of rejection at 1 month in two patients, one of whom developed chronic active antibody-mediated rejection 4.5 years later. One patient developed borderline acute cellular rejection at 1 month, but the serum creatinine level was stable and DSA disappeared without treatment 1 month later, with stable long-term allograft function at 3 years. Estimated or measured glomerular filtration rate of the patients ranged between 30 and 75 ml/min/1.73 m(2) after 1 to 4.5 years.
Conclusions:
The four sensitized patients reported here who received desensitization therapy had successful renal transplants with a low risk of immediate post-transplant rejection. Overall, long-term allograft functions and complications from immunosuppression were encouraging.
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