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Published on: May 10, 2017
Post-transplant lymphoproliferative disease in pediatric solid organ transplant recipients
Birte Wistinghausen1, Thomas G Gross, Catherine Bollard
1Jack Martin Division of Pediatric Hematology-Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. birte.wistinghausen@mssm.edu
Insights
Post-transplant lymphoproliferative disease (PTLD) is a common childhood complication after solid organ transplants (SOT). While heterogeneous, PTLD is often Epstein Barr virus-positive and manageable with current and novel therapies.
Area of Science:
- Pediatric Oncology
- Transplant Immunology
- Hematology
Background:
- Post-transplant lymphoproliferative disease (PTLD) is a significant complication in pediatric solid organ transplant (SOT) recipients.
- It represents a common form of lymphoproliferation in this vulnerable population.
- Over 90% of PTLD cases are B-cell in origin and Epstein Barr virus (EBV)-positive, typically emerging early post-transplant.
Purpose of the Study:
- To review the characteristics of PTLD in SOT recipients.
- To discuss current and emerging therapeutic strategies for PTLD.
- To highlight the heterogeneity and prognosis of PTLD.
Main Methods:
- Literature review of PTLD in SOT recipients.
- Analysis of pathological and clinical presentations.
- Discussion of treatment modalities including immunosuppression reduction, rituximab, and EBV-specific cytotoxic T-lymphocytes.
Main Results:
- PTLD is a heterogeneous condition with variable clinical courses.
- The majority of cases are EBV-positive B-cell lymphoproliferation.
- Prognosis is generally favorable, with a range of therapeutic responses.
Conclusions:
- PTLD management requires tailored approaches based on disease characteristics.
- Reduced immunosuppression is a primary intervention for many cases.
- Novel immune-based therapies show promise for refractory or aggressive PTLD.
Abstract:
Post-transplant lymphoproliferative disease (PTLD) in solid organ transplant (SOT) recipients has become one of the most common forms of lymphoproliferation in childhood and is a serious complication of SOT. More than 90% of cases are of B-cell origin, Epstein Barr virus (EBV) positive and are mostly occurring in the early post-transplant period. Pathologically and clinically it is a heterogenous disease ranging from being responsive to reduced immunosuppression without further intervention to rapidly progressive fulminant PTLD requiring prompt initiation of therapy. Prognosis overall is favorable. Current treatment strategies as well new promising targeted immune-based therapies such as rituximab and EBV-specific cytotoxic T-lymphocytes are being discussed.
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