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Updated: Jun 8, 2026

Intrafemoral Injection of Human Hematopoietic Stem and Progenitor Cells into Immunocompromised Mice
Published on: December 8, 2023
Solid organ transplants following hematopoietic stem cell transplant in children
Nancy Bunin1, Virginia Guzikowski, Elizabeth R Rand
1Divisions of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA. buninn@email.chop.edu
Insights
Solid organ transplantation (SOT) can be a viable option for children with permanent organ failure after hematopoietic stem cell transplantation (HSCT). Most patients in this study survived with functioning organs, highlighting SOT
Area of Science:
- Pediatric Hematology/Oncology
- Transplantation Medicine
- Immunology
Background:
- Hematopoietic stem cell transplantation (HSCT) is a curative therapy for various pediatric diseases.
- Permanent organ failure can occur post-HSCT, necessitating alternative treatment strategies.
- Solid organ transplantation (SOT) is a potential, yet understudied, option for these complex cases.
Purpose of the Study:
- To evaluate the outcomes of pediatric patients undergoing SOT after HSCT.
- To identify factors influencing SOT success in the post-HSCT population.
Main Methods:
- Retrospective review of eight pediatric patients who received SOT after HSCT at a single center.
- Analysis of patient demographics, underlying HSCT indications, time from HSCT to SOT, SOT type, and patient survival.
- Review of complications and graft function.
Main Results:
- Seven out of eight patients survived with functioning allografts between 6 to 180 months post-SOT.
- Indications for HSCT included genetic disorders, bone marrow failure syndromes, and malignancies.
- Transplanted organs included lungs, kidneys, and liver, with indications such as Bronchiolitis Obliterans, VOD, and chronic GVHD.
Conclusions:
- SOT can be successful in select pediatric patients with organ failure following HSCT.
- Advances in transplantation techniques and supportive care improve outcomes.
- Donor organ availability remains a significant challenge, and careful patient selection is crucial for success.
Abstract:
SOT may be indicated for a select group of pediatric patients who experience permanent organ failure following HSCT. However, there is limited information available about outcomes. We identified eight children at our center who received an SOT following an HSCT. Patients were six months to 18 yr at HSCT. Diseases for which children underwent HSCT included thalassemia, Wiskott-Aldrich syndrome, Shwachman-Diamond/bone marrow failure, sickle cell disease (SCD), erythropoietic porphyria (EP), ALL, chronic granulomatous disease, and neuroblastoma. Time from HSCT to SOT was 13 days to seven yr (median, 27 months. Lung SOT was performed for two patients with BO, kidney transplants for three patients, and liver transplants for three patients (VOD, chronic GVHD). Seven patients are alive with functioning allografts 6-180 months from SOT. Advances in organ procurement, operative technique, immunosuppressant therapy, and infection control may allow SOT for a select group of patients post-HSCT. However, scarcity of donor organs available in a timely fashion continues to be a limiting factor. Children who have undergone HSCT and develop single organ failure should be considered for an SOT if there is a high likelihood of cure of the primary disease.
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