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Updated: Mar 3, 2026

Murine Kidney Transplant Technique
Published on: October 20, 2015
Kidney transplant after hematopoietic cell transplant in pediatrics: Infectious and immunosuppressive considerations
Christen L Ebens1, Angela R Smith1, Priya S Verghese2
1Department of Pediatrics, Division of Blood and Marrow Transplant, University of Minnesota, Minneapolis, MN, USA.
Insights
Pediatric kidney transplant (KTx) recipients after hematopoietic cell transplant (HCT) face high infection risks. Optimizing immune reconstitution and using non-T-cell-depleting therapies can improve outcomes for these vulnerable patients.
Area of Science:
- Pediatric Nephrology
- Transplant Immunology
- Infectious Diseases
Background:
- Pediatric kidney transplant (KTx) after hematopoietic cell transplant (HCT) involves significant immunosuppression, increasing infection risk.
- Understanding risk factors for infectious complications in this unique patient population is crucial for improving outcomes.
Observation:
- A review of four pediatric post-HCT KTx patients revealed universal viremia (BK virus, Epstein-Barr virus, human herpesvirus-6), with one fatality.
- In contrast, five similar cases from the literature reported no viremia.
Findings:
- Key risk factors for severe infections include lymphodepleting serotherapy during HCT conditioning, multiple HCTs, short immune reconstitution intervals, high pre-KTx viral loads, and T-cell-depleting induction immunosuppression for KTx.
- Pediatric post-HCT KTx recipients exhibit a heightened susceptibility to viral infections.
Implications:
- Thorough pre-KTx immune reconstitution assessment and the use of non-T-cell-depleting induction therapy for KTx are recommended for pediatric post-HCT KTx patients.
- These strategies were successfully applied to a subsequent patient, resulting in excellent outcomes one year post-KTx.
Abstract:
Pediatric patients requiring kidney transplant after hematopoietic cell transplant receive multiple courses of immunosuppression placing them at risk for infection. To elucidate potential risk factors for infection, we compared the immunosuppressive regimens and infectious complications of pediatric kidney transplant recipients at a single institution who had previously undergone hematopoietic cell transplant from different donors to similar patients reported in the literature. Among the initial four post-hematopoietic cell transplant kidney transplant patients reviewed, viremia episodes were universal, including BK virus, Epstein-Barr virus, and human herpesvirus-6, with one death from presumed BK virus encephalitis. No viremia was reported in five similar cases in the literature. Risk factors for increased infection include use of lymphodepleting serotherapy in HCT conditioning, multiple HCTs, limited immune reconstitution time between transplants, increased pre-KTx viral burden, and use of T-cell-depleting versus -suppressive induction immunosuppression for KTx. These findings suggest that pediatric post-HCT KTx recipients are at increased risk for viral infections, likely benefitting from thorough pre-KTx evaluation of immune reconstitution and preferential use of non-T-cell-depleting induction therapy for KTx. We applied these recommendations to one subsequent post-HCT patient requiring KTx at our institution with excellent outcomes one year post-KTx.
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