Preserved renal-allograft function and the PD-1 pathway inhibitor nivolumab
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To the Editor: Inhibition of immune checkpoints with the use of antibodies targeting programmed cell death 1 (PD-1) or monoclonal antibodies against cytotoxic T-lymphocyte–associated antigen 4 (CTLA-4) has been used clinically in patients with various types of cancer. In the limited number of reported cases in which these antibodies have been used in patients who have undergone kidney transplantation,1 these agents have been associated with cell-mediated and antibody-mediated rejection (see Table S2 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). We report on a patient who received a renal transplant from a living related donor. . . .
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Several transplant patients experienced a tumor response without rejection when their immunosuppressive regimen contained sirolimus.
“Interestingly, several transplant patients experienced a tumor response without rejection when their immunosuppressive regimen contained sirolimus.165,169,170”
From Autoimmune diseases and immune-checkpoint inhibitors for cancer therapy: Review of the literature and personalized risk-based prevention strategy (2020) · cites this paper as [170]
Anecdotal use of mTOR inhibition as primary prevention was reported for patients with kidney transplants.
“For patients with kidney transplants, anecdotal use of mTOR inhibition (mTORi) as primary prevention was reported12,13.”
From Targeting the mTOR pathway uncouples the efficacy and toxicity of PD-1 blockade in renal transplantation (2019) · cites this paper as [13]
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A novel approach to candidemia? The potential role of checkpoint inhibition
Mellinghoff, S. C., von Bergwelt‐Baildon, M., Schößer, H. A., & Cornely, O. A. (2018) · Medical Mycology · doi:10.1093/mmy/myy089 · Cited by 12 · see citing works
Immune checkpoint inhibitor induced nephrotoxicity: An ongoing challenge
Catalano, M., Roviello, G., Galli, I. C., Santi, R., & Nesi, G. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.1014257 · Cited by 10 · see citing works
Bolufer, M., Soler-Majoral, J., Molina, M., Taco, O., Vila, A., & Macía, M. (2024) · Transplant International · doi:10.3389/ti.2024.13204 · Cited by 10 · see citing works
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Toxicités rénales des inhibiteurs des points de contrôle de l’auto-immunité
Izzedine, H., & Gueutin, V. (2019) · Néphrologie & Thérapeutique · doi:10.1016/j.nephro.2019.05.006 · Cited by 8 · see citing works
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The successful use of pembrolizumab in a renal transplant recipient with metastatic melanoma
Hanna, D., Law, S., Merrick, S., Heptinstall, L., Bass, P., Dupont, P. J., & Sheri, A. (2019) · Melanoma Research · doi:10.1097/cmr.0000000000000651 · Cited by 8 · see citing works
Immunotherapies and renal injury
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- Authors
- Barnett, R., Barta, V. S., & Jhaveri, K. D.
- Affiliations
- Hofstra University (US)
- ORCID
- Jhaveri, Kenar D.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2017-01-12
- Volume
- 376
- Issue
- 2
- Pages
- 191-192
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2578082697
- Cited by
- 136
- References
- 5
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 14 · 2023: 6 · 2022: 18 · 2021: 12 · 2020: 26 · 2019: 16 · 2018: 21 · 2017: 17
- FWCI
- 18.48
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Transplantation › Renal Transplantation Outcomes and Treatments
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
- Keywords
- nivolumab, kidney transplantation, immune checkpoint inhibitors, graft rejection, antibody-mediated rejection, cell-mediated rejection, living related donors, renal allograft function
- MeSH terms
- Nivolumab, Adenocarcinoma, Aged, Antibodies, Monoclonal, Antineoplastic Agents, Duodenal Neoplasms, Humans, Liver Neoplasms, Male, Kidney Transplantation, Programmed Cell Death 1 Receptor
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