Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies
Chemotherapy-associated renal injury is considered one of the major concerns among nephrological and oncological practice. The use of novel anti-neoplastic therapies that target carcinomas has helped in the detection of this form of renal injury. Immune checkpoint inhibitors (ICPIs) are a group of m...
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Society of Diabetic Nephropathy Prevention
2021-05-01
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doaj-0af70647cf4946cf85303b48b4749d122021-09-14T18:03:08ZengSociety of Diabetic Nephropathy Prevention Journal of Nephropharmacology2345-42022021-05-01102e22e2210.34172/npj.2021.22npj-10416Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studiesTella Sadighpour0Celeste Cagnazzo1Shahrzad Alimohammadi2Anahita Emami3Azadeh Khayyat4Mohammad Ali EsmaeilPour5Florida International University, Herbert Wertheim College of Medicine, Miami, Florida, USAResearch and Clinical Development Unit, Pediatric Oncology and Hematology Unit, University of Turin, Turin, ItalyDoctoral School of Molecular Medicine, University of Debrecen, Debrecen, HungaryIndependent Researcher, 12 Leadenhall Road, Toronto, Ontario, CanadaIndependent Researcher 4246 Graveley St., Burnaby, BC, CanadaAdventhealth Graduate Medical Education, Center for Collaborative Research, Orlando, Florida, USAChemotherapy-associated renal injury is considered one of the major concerns among nephrological and oncological practice. The use of novel anti-neoplastic therapies that target carcinomas has helped in the detection of this form of renal injury. Immune checkpoint inhibitors (ICPIs) are a group of monoclonal antibodies targeting inhibitory receptors that exist on tumor cells and T cells. ICPIs are able to suppress tumors that might have escaped from the immune surveillance. Meanwhile, although ICPIs have shown promising efficacy in cancer treatment, their immune-related side effects limit their widespread use in cancer therapy schedules. One of the major side effects limiting ICPIs’ usage is nephrotoxicity. Glomerular disease, acute interstitial nephritis (AIN), and acute tubular necrosis (ATN) are considered different infusion-related adverse events. Infiltration of eosinophils, T lymphocytes, and plasma cells, as well as interstitial inflammation and edema, leading to acute tubulointerstitial nephritis (ATIN). It is conceivable that the rupture of self-tolerance by ICPIs induces an autoimmune reaction against some specific self-antigens in the organs including kidneys. The exact nature of the antigen is unclear; however, it is possible that it is found in the renal tubular cells, as indicated by a greater frequency of ATIN in kidney biopsies. The current review paper discusses the relationship between ICPIs therapy and kidney disorders or more specifically, their possible role in renal damage along with renal toxicity profile in the setting of ICPIs treatment.https://jnephropharmacology.com/PDF/npj-10416immunotherapyglomerular filtration ratecheckpoint inhibitorsglomerulonephritisacute interstitial nephritisacute tubular necrosisacute renal failureimmune-related adverse eventsacute tubulointerstitial nephritis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tella Sadighpour Celeste Cagnazzo Shahrzad Alimohammadi Anahita Emami Azadeh Khayyat Mohammad Ali EsmaeilPour |
spellingShingle |
Tella Sadighpour Celeste Cagnazzo Shahrzad Alimohammadi Anahita Emami Azadeh Khayyat Mohammad Ali EsmaeilPour Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies Journal of Nephropharmacology immunotherapy glomerular filtration rate checkpoint inhibitors glomerulonephritis acute interstitial nephritis acute tubular necrosis acute renal failure immune-related adverse events acute tubulointerstitial nephritis |
author_facet |
Tella Sadighpour Celeste Cagnazzo Shahrzad Alimohammadi Anahita Emami Azadeh Khayyat Mohammad Ali EsmaeilPour |
author_sort |
Tella Sadighpour |
title |
Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
title_short |
Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
title_full |
Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
title_fullStr |
Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
title_full_unstemmed |
Immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
title_sort |
immune-related adverse kidney events by immune checkpoint inhibitors; a narrative review on current studies |
publisher |
Society of Diabetic Nephropathy Prevention |
series |
Journal of Nephropharmacology |
issn |
2345-4202 |
publishDate |
2021-05-01 |
description |
Chemotherapy-associated renal injury is considered one of the major concerns among nephrological and oncological practice. The use of novel anti-neoplastic therapies that target carcinomas has helped in the detection of this form of renal injury. Immune checkpoint inhibitors (ICPIs) are a group of monoclonal antibodies targeting inhibitory receptors that exist on tumor cells and T cells. ICPIs are able to suppress tumors that might have escaped from the immune surveillance. Meanwhile, although ICPIs have shown promising efficacy in cancer treatment, their immune-related side effects limit their widespread use in cancer therapy schedules. One of the major side effects limiting ICPIs’ usage is nephrotoxicity. Glomerular disease, acute interstitial nephritis (AIN), and acute tubular necrosis (ATN) are considered different infusion-related adverse events. Infiltration of eosinophils, T lymphocytes, and plasma cells, as well as interstitial inflammation and edema, leading to acute tubulointerstitial nephritis (ATIN). It is conceivable that the rupture of self-tolerance by ICPIs induces an autoimmune reaction against some specific self-antigens in the organs including kidneys. The exact nature of the antigen is unclear; however, it is possible that it is found in the renal tubular cells, as indicated by a greater frequency of ATIN in kidney biopsies. The current review paper discusses the relationship between ICPIs therapy and kidney disorders or more specifically, their possible role in renal damage along with renal toxicity profile in the setting of ICPIs treatment. |
topic |
immunotherapy glomerular filtration rate checkpoint inhibitors glomerulonephritis acute interstitial nephritis acute tubular necrosis acute renal failure immune-related adverse events acute tubulointerstitial nephritis |
url |
https://jnephropharmacology.com/PDF/npj-10416 |
work_keys_str_mv |
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