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Updated: Feb 26, 2026

Investigating the Immunological Mechanisms Underlying Organ Transplant Rejection
Published on: August 20, 2007
Immune Checkpoint Inhibitors in Organ Transplant Patients
Adam S Kittai1, Hayden Oldham, Jeremy Cetnar
1Departments of *Hematology and Medical Oncology†Internal Medicine, Oregon Health & Science University, Portland, OR.
Abstract:
Modulation of T-cell activity through blockade of coinhibitory molecules has revolutionized the treatment of various malignancies. Several immune checkpoint inhibitors are currently Food and Drug Administration approved which target various coinhibitory pathways including cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death 1 receptor (PD-1), and programmed cell death ligand-1. Clinical trials that lead to the Food and Drug Administration approval of these agents often excluded patients with an organ transplant. Excluding these patients was deliberate due to concern that immune checkpoint inhibitor therapy could lead to graft rejection. The PD-1 and CTLA-4 pathways are essential to downregulate our immune system in the setting of T-cell activation to prevent autoimmunity. Furthermore, both pathways are implicated in transplanted organ tolerance and modulation of the pathways may inadvertently lead to peripheral transplant rejection. Currently, there are no guidelines for the treatment of patients with immune checkpoint inhibitors in the setting of a prior organ transplant. Thus far, there are only 10 reported cases of patients in the literature who were treated in this setting. Two additional cases are reported herein, including 1 patient with a prior cardiac transplant receiving nivolumab for non-small cell lung cancer. Of the 12 cases, 4 patients experienced organ rejection. From these observations, the authors hypothesize factors that affect safety and of this treatment modality in this patient population. These factors include the integral role of the PD-1 pathway compared with the CTLA-4 pathway in organ acceptance, sequential implementation of different immune checkpoint inhibitor classes, length of time with a transplant before therapy, strength of immunosuppressive agents to prevent organ transplant rejection, and immunogenicity of the particular organ grafted. Although limited cases have been reported, there are circumstances in which immune checkpoint inhibitors have been used in the setting of organ transplantation without resulting in organ rejection. A thorough discussion with the patient of the potential risks, including graft rejection, and benefits of this therapy is necessary before beginning this treatment. More research is needed to explore the safety and efficacy of immune checkpoint inhibitors in the setting of organ transplantation.
Insights
Immune checkpoint inhibitors, used for cancer, may risk organ transplant rejection. Careful patient discussion and further research are crucial for safe use in transplant recipients.
Area of Science:
- Oncology and Immunology
- Transplant Medicine
Background:
- Immune checkpoint inhibitors (ICIs) targeting CTLA-4 and PD-1 pathways have transformed cancer therapy.
- Patients with organ transplants were excluded from clinical trials due to concerns about graft rejection.
- Both CTLA-4 and PD-1 pathways are vital for immune regulation and transplant tolerance.
Observation:
- Limited data exists on ICI use in organ transplant recipients; only 12 cases reported.
- Four out of 12 patients experienced organ rejection after ICI therapy.
- One case involved a cardiac transplant recipient treated with nivolumab for lung cancer.
Findings:
- Factors influencing ICI safety in transplant patients include PD-1 vs. CTLA-4 pathway involvement, ICI sequencing, time since transplant, immunosuppression strength, and organ immunogenicity.
- Some patients have received ICIs post-transplant without rejection.
- No current guidelines exist for managing ICIs in this population.
Implications:
- Thorough patient counseling on risks (graft rejection) and benefits is essential before initiating ICI therapy.
- Further research is required to establish safety and efficacy of ICIs in organ transplant recipients.
- Understanding ICI impact on transplant tolerance is critical for future treatment strategies.
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