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Published on: February 17, 2022
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CAR-T for Management of R/R PTLD Following Lung Transplant: A Multi-center Retrospective Study
Brittany Salter1, Adam Suleman2, Robert Kridel3
1Department of Oncology, Juravinski Hospital & Cancer Centre, Hamilton, Ontario, Canada.
Transplantation and Cellular Therapy
|October 11, 2025
Summary
Chimeric antigen receptor T-cell (CAR-T) therapy shows promise for treating post-transplant lymphoproliferative disorder (PTLD) in lung transplant recipients. This study found CAR-T therapy effective with manageable side effects in three patients with relapsed/refractory PTLD.
Area of Science:
- Oncology
- Immunology
- Transplantation
Background:
- Post-transplant lymphoproliferative disorder (PTLD) is a rare malignancy after solid organ transplantation (SOT), with lung transplant recipients facing high mortality.
- CD19-directed chimeric antigen receptor T-cell (CAR-T) therapy is effective for relapsed/refractory B-cell lymphoma, but its use in PTLD, especially post-lung SOT, is not well-established.
Purpose of the Study:
- To evaluate the feasibility and efficacy of Axicabtagene ciloleucel (Axicel) CAR-T therapy in lung transplant recipients with relapsed/refractory PTLD.
- To assess the safety and toxicity profile of CAR-T therapy in this specific patient population.
- To explore the optimal management of immunosuppression (IST) around CAR-T infusion to balance efficacy and allograft preservation.
Main Methods:
- A multi-center retrospective study involving three lung transplant recipients with relapsed/refractory PTLD treated with Axicel.
- Review of prior therapies, CAR-T treatment course, response, toxicity, and immunosuppression management.
- Analysis of cytokine release syndrome (CRS) and allograft outcomes.
Main Results:
- All three patients achieved complete or partial response to CAR-T therapy.
- Cytokine release syndrome (CRS) was observed in all patients but was mild and effectively managed.
- One patient experienced allograft rejection, highlighting the need for careful IST modification.
Conclusions:
- CAR-T therapy is a feasible treatment option for lung SOT recipients with PTLD, demonstrating promising responses and manageable toxicities.
- Individualized modification of immunosuppression around CAR-T infusion is crucial for balancing treatment efficacy with lung allograft preservation.
- Further research is needed to understand IST management in this complex patient subset, as current CAR-T studies often exclude them.

