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Belatacept Conversion in Kidney After Liver Transplantation
BACKGROUND. Costimulatory blockade with belatacept has demonstrated long-term benefits in renal transplantation, but de novo use in liver transplant recipients has resulted in increased rejection, graft loss, and death. However, belatacept conversion as a calcineurin inhibitor (CNI) avoidance strate...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547931/ https://www.ncbi.nlm.nih.gov/pubmed/34712780 http://dx.doi.org/10.1097/TXD.0000000000001229 |
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author | Cristea, Octav Karadkhele, Geeta Kitchens, William H. Vasanth, Payaswini Larsen, Christian P. Badell, Idelberto R. |
author_facet | Cristea, Octav Karadkhele, Geeta Kitchens, William H. Vasanth, Payaswini Larsen, Christian P. Badell, Idelberto R. |
author_sort | Cristea, Octav |
collection | PubMed |
description | BACKGROUND. Costimulatory blockade with belatacept has demonstrated long-term benefits in renal transplantation, but de novo use in liver transplant recipients has resulted in increased rejection, graft loss, and death. However, belatacept conversion as a calcineurin inhibitor (CNI) avoidance strategy has not been studied and may be of benefit in liver transplantation where CNI-induced renal dysfunction and toxicity are barriers to improved outcomes. METHODS. Using clinical data extracted from our institutional medical record, we report on 8 patients who underwent kidney after liver transplantation and were treated with belatacept-based immunosuppression and transient CNI therapy. RESULTS. All patients tolerated belatacept therapy without any patient deaths or graft losses. No episodes of rejection, de novo donor-specific antibody formation, or major systemic infections were observed, and all patients demonstrated preserved liver and excellent renal allograft function. Patients received belatacept for a median duration of 13.2 mo, and at a median follow-up of 15.9 mo post–kidney transplant, 6 of 8 patients continued on belatacept with 3 completely off and 3 poised to transition off CNI. CONCLUSIONS. These findings are the first evidence that in liver transplant recipients requiring subsequent kidney transplantation, belatacept-based therapy can potentially facilitate CNI-free maintenance immunosuppression. This supports the possibility of belatacept conversion in stand-alone liver transplant recipients as a viable method of CNI avoidance. |
format | Online Article Text |
id | pubmed-8547931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-85479312021-10-27 Belatacept Conversion in Kidney After Liver Transplantation Cristea, Octav Karadkhele, Geeta Kitchens, William H. Vasanth, Payaswini Larsen, Christian P. Badell, Idelberto R. Transplant Direct Kidney Transplantation BACKGROUND. Costimulatory blockade with belatacept has demonstrated long-term benefits in renal transplantation, but de novo use in liver transplant recipients has resulted in increased rejection, graft loss, and death. However, belatacept conversion as a calcineurin inhibitor (CNI) avoidance strategy has not been studied and may be of benefit in liver transplantation where CNI-induced renal dysfunction and toxicity are barriers to improved outcomes. METHODS. Using clinical data extracted from our institutional medical record, we report on 8 patients who underwent kidney after liver transplantation and were treated with belatacept-based immunosuppression and transient CNI therapy. RESULTS. All patients tolerated belatacept therapy without any patient deaths or graft losses. No episodes of rejection, de novo donor-specific antibody formation, or major systemic infections were observed, and all patients demonstrated preserved liver and excellent renal allograft function. Patients received belatacept for a median duration of 13.2 mo, and at a median follow-up of 15.9 mo post–kidney transplant, 6 of 8 patients continued on belatacept with 3 completely off and 3 poised to transition off CNI. CONCLUSIONS. These findings are the first evidence that in liver transplant recipients requiring subsequent kidney transplantation, belatacept-based therapy can potentially facilitate CNI-free maintenance immunosuppression. This supports the possibility of belatacept conversion in stand-alone liver transplant recipients as a viable method of CNI avoidance. Lippincott Williams & Wilkins 2021-10-22 /pmc/articles/PMC8547931/ /pubmed/34712780 http://dx.doi.org/10.1097/TXD.0000000000001229 Text en Copyright © 2021 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Kidney Transplantation Cristea, Octav Karadkhele, Geeta Kitchens, William H. Vasanth, Payaswini Larsen, Christian P. Badell, Idelberto R. Belatacept Conversion in Kidney After Liver Transplantation |
title | Belatacept Conversion in Kidney After Liver Transplantation |
title_full | Belatacept Conversion in Kidney After Liver Transplantation |
title_fullStr | Belatacept Conversion in Kidney After Liver Transplantation |
title_full_unstemmed | Belatacept Conversion in Kidney After Liver Transplantation |
title_short | Belatacept Conversion in Kidney After Liver Transplantation |
title_sort | belatacept conversion in kidney after liver transplantation |
topic | Kidney Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547931/ https://www.ncbi.nlm.nih.gov/pubmed/34712780 http://dx.doi.org/10.1097/TXD.0000000000001229 |
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