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Conversion to belatacept after lung transplantation: Report of 10 cases
BACKGROUND: Calcineurin inhibitors (CNIs) remain the cornerstone of maintenance immunosuppression (IS) after lung transplantation (LTx), although CNI-related life-threatening toxic effects may occur. Belatacept, a novel immunosuppressant that blocks a T-cell co-stimulation pathway, is a non-nephroto...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016650/ https://www.ncbi.nlm.nih.gov/pubmed/36920935 http://dx.doi.org/10.1371/journal.pone.0281492 |
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author | Brugière, Olivier Vallée, Alexandre Raimbourg, Quentin Peraldi, Marie-Noelle de Verdière, Sylvie Colin Beaumont, Laurence Hamid, Abdulmonem Zrounba, Mathilde Roux, Antoine Picard, Clément Parquin, François Glorion, Matthieu Oniszczuk, Julie Hertig, Alexandre Mal, Hervé Bunel, Vincent |
author_facet | Brugière, Olivier Vallée, Alexandre Raimbourg, Quentin Peraldi, Marie-Noelle de Verdière, Sylvie Colin Beaumont, Laurence Hamid, Abdulmonem Zrounba, Mathilde Roux, Antoine Picard, Clément Parquin, François Glorion, Matthieu Oniszczuk, Julie Hertig, Alexandre Mal, Hervé Bunel, Vincent |
author_sort | Brugière, Olivier |
collection | PubMed |
description | BACKGROUND: Calcineurin inhibitors (CNIs) remain the cornerstone of maintenance immunosuppression (IS) after lung transplantation (LTx), although CNI-related life-threatening toxic effects may occur. Belatacept, a novel immunosuppressant that blocks a T-cell co-stimulation pathway, is a non-nephrotoxic drug indicated as an alternative to CNIs in kidney Tx. In LTx, there are only a few reports of belatacept conversion as a CNI-free or CNI-sparing IS treatment. METHODS: We reviewed a series of 10 LTx recipients with conversion to a CNI-free belatacept IS regimen within the first year post-LTx (n = 7) or a belatacept/low-dose CNI combination after the first year (n = 3). RESULTS: Use of belatacept was triggered by severe renal failure in 9 patients and under-IS with previous other IS-related toxicities in 1 patient. Mean estimated glomerular filtration rate after starting belatacept significantly improved at 6 months after initiation and at the last-follow-up (p = 0.006, and p = 0.002 respectively). The incidence of recurrent and/or severe acute cellular rejection (ACR) episodes was high in patients with CNI-free belatacept-based IS (n = 4/7). Chronic graft allograft dysfunction developed in 2 of 9 recipients under belatacept IS. Belatacept was stopped in 6 patients because of recurrent/severe ACR (n = 3), recurrent opportunistic infections (n = 1), center modified policy (n = 1), or other cause (n = 1). CONCLUSION: Early conversion to CNI-free belatacept-based IS improved renal function in this series but was counterbalanced by a high incidence of recurrent ACR, including life-threatening episodes. Other studies are needed to better determine the indications for its use after LTx, possibly with lower immunological risk IS regimens, such as CNI-sparing belatacept. |
format | Online Article Text |
id | pubmed-10016650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100166502023-03-16 Conversion to belatacept after lung transplantation: Report of 10 cases Brugière, Olivier Vallée, Alexandre Raimbourg, Quentin Peraldi, Marie-Noelle de Verdière, Sylvie Colin Beaumont, Laurence Hamid, Abdulmonem Zrounba, Mathilde Roux, Antoine Picard, Clément Parquin, François Glorion, Matthieu Oniszczuk, Julie Hertig, Alexandre Mal, Hervé Bunel, Vincent PLoS One Research Article BACKGROUND: Calcineurin inhibitors (CNIs) remain the cornerstone of maintenance immunosuppression (IS) after lung transplantation (LTx), although CNI-related life-threatening toxic effects may occur. Belatacept, a novel immunosuppressant that blocks a T-cell co-stimulation pathway, is a non-nephrotoxic drug indicated as an alternative to CNIs in kidney Tx. In LTx, there are only a few reports of belatacept conversion as a CNI-free or CNI-sparing IS treatment. METHODS: We reviewed a series of 10 LTx recipients with conversion to a CNI-free belatacept IS regimen within the first year post-LTx (n = 7) or a belatacept/low-dose CNI combination after the first year (n = 3). RESULTS: Use of belatacept was triggered by severe renal failure in 9 patients and under-IS with previous other IS-related toxicities in 1 patient. Mean estimated glomerular filtration rate after starting belatacept significantly improved at 6 months after initiation and at the last-follow-up (p = 0.006, and p = 0.002 respectively). The incidence of recurrent and/or severe acute cellular rejection (ACR) episodes was high in patients with CNI-free belatacept-based IS (n = 4/7). Chronic graft allograft dysfunction developed in 2 of 9 recipients under belatacept IS. Belatacept was stopped in 6 patients because of recurrent/severe ACR (n = 3), recurrent opportunistic infections (n = 1), center modified policy (n = 1), or other cause (n = 1). CONCLUSION: Early conversion to CNI-free belatacept-based IS improved renal function in this series but was counterbalanced by a high incidence of recurrent ACR, including life-threatening episodes. Other studies are needed to better determine the indications for its use after LTx, possibly with lower immunological risk IS regimens, such as CNI-sparing belatacept. Public Library of Science 2023-03-15 /pmc/articles/PMC10016650/ /pubmed/36920935 http://dx.doi.org/10.1371/journal.pone.0281492 Text en © 2023 Brugière et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Brugière, Olivier Vallée, Alexandre Raimbourg, Quentin Peraldi, Marie-Noelle de Verdière, Sylvie Colin Beaumont, Laurence Hamid, Abdulmonem Zrounba, Mathilde Roux, Antoine Picard, Clément Parquin, François Glorion, Matthieu Oniszczuk, Julie Hertig, Alexandre Mal, Hervé Bunel, Vincent Conversion to belatacept after lung transplantation: Report of 10 cases |
title | Conversion to belatacept after lung transplantation: Report of 10 cases |
title_full | Conversion to belatacept after lung transplantation: Report of 10 cases |
title_fullStr | Conversion to belatacept after lung transplantation: Report of 10 cases |
title_full_unstemmed | Conversion to belatacept after lung transplantation: Report of 10 cases |
title_short | Conversion to belatacept after lung transplantation: Report of 10 cases |
title_sort | conversion to belatacept after lung transplantation: report of 10 cases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016650/ https://www.ncbi.nlm.nih.gov/pubmed/36920935 http://dx.doi.org/10.1371/journal.pone.0281492 |
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