Prevention of post-transplant lymphoproliferative disorder in pediatric kidney transplant recipients
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Updated: Jun 11, 2025

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Shirley Pollack1,2, Moran Plonsky3,4, Rami Tibi4
1Technion Faculty of Medicine, Haifa, Israel. s_pollack@technion.ac.il.
Insights
Preventive rituximab therapy may safely clear Epstein-Barr virus (EBV) DNA and prevent post-transplant lymphoproliferative disorder (PTLD) in pediatric kidney transplant recipients (PKTR), especially those EBV-naïve pre-transplant.
Area of Science:
- Immunology
- Transplantation Medicine
- Virology
Background:
- Post-transplant lymphoproliferative disorder (PTLD) is a serious complication following solid organ transplantation (SOT) and hematopoietic stem cell transplantation (HSCT).
- Epstein-Barr virus (EBV) infection is a precursor to PTLD in most cases.
- Rituximab, an anti-CD20 antibody, targets EBV-infected B-lymphocytes and is used for PTLD prevention in HSCT but not established in SOT.
Purpose of the Study:
- To evaluate the safety and efficacy of preventive rituximab therapy for Epstein-Barr virus (EBV) DNAemia in pediatric kidney transplant recipients (PKTR).
- To assess EBV clearance and PTLD prevention strategies in EBV-seronegative PKTR.
Main Methods:
- Routine EBV-PCR surveillance was performed on pediatric kidney transplant recipients (PKTR).
- Patients with rising EBV viral loads, unresponsive to immunosuppression dose reduction, received preventive rituximab therapy.
- Outcomes including EBV PCR clearance and complications were monitored.
Main Results:
- Eleven percent (7/65) of PKTR developed asymptomatic EBV DNAemia between 120-720 days post-transplant.
- Seventy-one percent (5/7) of patients with EBV DNAemia were EBV-seronegative pre-transplant.
- All patients treated with rituximab achieved EBV PCR clearance with minimal complications.
Conclusions:
- Pediatric kidney transplant recipients (PKTR) who are EBV-naïve pre-transplant have a higher incidence of EBV DNAemia.
- Immunosuppression dose reduction is less effective for EBV clearance in EBV-seronegative PKTR.
- Preventive rituximab therapy appears safe and effective for EBV clearance and PTLD prevention in PKTR.
Background:
Post-transplant lymphoproliferative disorder (PTLD) is a devastating complication of immunosuppressive treatment in both solid organ transplantations (SOT) and hematopoietic stem cell transplantations (HSCT). Epstein-Barr virus (EBV) infection precedes PTLD in 90% of patients. Rituximab, a monoclonal anti-CD20 antibody, depletes B-lymphocytes, which are the ultimate reservoir for EBV. Although rituximab therapy is commonly used as a preventive measure for PTLD in high-risk HSCT, it is not established in SOT.
Methods:
Pediatric kidney transplant recipients (PKTR) underwent routine EBV-PCR surveillance. Patients with increasing viral loads, despite immunosuppressive dose reduction, were managed with preventive rituximab therapy.
Results:
Between 2012 and 2023, we identified eight episodes of asymptomatic EBV-PCR-positive blood tests in seven out of 65 PKTR (11%) under our care. EBV DNAemia emerged 120-720 days post-transplantation. Five of seven patients with EBV DNAemia (71%) were EBV-seronegative prior to transplantation. All five patients did not respond to MMF dose reduction and were therefore treated with preventive rituximab therapy. Following this treatment, EBV PCR clearance was observed in all patients with only minimal complications.
Conclusions:
PKTR who are EBV-naïve prior to transplantation are expected to have a higher prevalence of EBV DNAemia. We found that PKTR who were EBV seronegative prior to transplantation were less likely to achieve EBV clearance in response to immunosuppression dose reduction. We suggest that rituximab therapy in PKTR may be safe and effective in EBV clearance and PTLD prevention.
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