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Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients

BACKGROUND: The efficacy and safety of minimisation of immunosuppression including early steroid withdrawal in kidney transplant recipients treated with Basiliximab induction remains unclear. METHODS: This retrospective cohort study reports the outcomes from 298 consecutive renal transplants perform...

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Autores principales: Phanish, Mysore K., Hull, Richard P., Andrews, Peter A., Popoola, Joyce, Kingdon, Edward J., MacPhee, Iain A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065371/
https://www.ncbi.nlm.nih.gov/pubmed/32160893
http://dx.doi.org/10.1186/s12882-020-01739-3
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author Phanish, Mysore K.
Hull, Richard P.
Andrews, Peter A.
Popoola, Joyce
Kingdon, Edward J.
MacPhee, Iain A. M.
author_facet Phanish, Mysore K.
Hull, Richard P.
Andrews, Peter A.
Popoola, Joyce
Kingdon, Edward J.
MacPhee, Iain A. M.
author_sort Phanish, Mysore K.
collection PubMed
description BACKGROUND: The efficacy and safety of minimisation of immunosuppression including early steroid withdrawal in kidney transplant recipients treated with Basiliximab induction remains unclear. METHODS: This retrospective cohort study reports the outcomes from 298 consecutive renal transplants performed since 1st July 2010–June 2013 treated with Basiliximab induction and early steroid withdrawal in low immunological risk patients using a simple immunological risk stratification and 3-month protocol biopsy to optimise therapy. The cohort comprised 225 low-risk patients (first transplant or HLA antibody calculated reaction frequency (CRF ≤50% with no donor specific HLA antibodies) who underwent basiliximab induction, steroid withdrawal on day 7 and maintenance with tacrolimus and mycophenolate mofetil (MMF), and 73 high-risk patients who received tacrolimus, MMF and prednisolone for the first 3 months followed by long term maintenance immunosuppression with tacrolimus and prednisolone. High-risk patients not undergoing 3-month protocol biopsy were continued on triple immunosuppression. RESULTS: Steroid withdrawal could be safely achieved in low immunological risk recipients with IL2 receptor antibody induction. The incidence of biopsy-proven acute rejection was 15.1% in the low-risk and 13.9% in the high-risk group (including sub-clinical rejection detected at protocol biopsy). One- year graft survival was 93.3% and patient survival 98.5% in the low-risk group, and 97.3 and 100% respectively in the high-risk group. Graft function was similar in each group at 1 year (mean eGFR 61.2 ± 23.4 mL/min low-risk and 64.6 ± 19.2 mL/min high-risk). CONCLUSIONS: Immunosuppression regimen comprising basiliximab induction, tacrolimus, MMF and prednisolone with early steroid withdrawal in low risk patients and MMF withdrawal in high risk patients following a normal 3-month protocol biopsy is effective in limiting acute rejection episodes and produces excellent rates of patient survival, graft function and complications.
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spelling pubmed-70653712020-03-16 Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients Phanish, Mysore K. Hull, Richard P. Andrews, Peter A. Popoola, Joyce Kingdon, Edward J. MacPhee, Iain A. M. BMC Nephrol Research Article BACKGROUND: The efficacy and safety of minimisation of immunosuppression including early steroid withdrawal in kidney transplant recipients treated with Basiliximab induction remains unclear. METHODS: This retrospective cohort study reports the outcomes from 298 consecutive renal transplants performed since 1st July 2010–June 2013 treated with Basiliximab induction and early steroid withdrawal in low immunological risk patients using a simple immunological risk stratification and 3-month protocol biopsy to optimise therapy. The cohort comprised 225 low-risk patients (first transplant or HLA antibody calculated reaction frequency (CRF ≤50% with no donor specific HLA antibodies) who underwent basiliximab induction, steroid withdrawal on day 7 and maintenance with tacrolimus and mycophenolate mofetil (MMF), and 73 high-risk patients who received tacrolimus, MMF and prednisolone for the first 3 months followed by long term maintenance immunosuppression with tacrolimus and prednisolone. High-risk patients not undergoing 3-month protocol biopsy were continued on triple immunosuppression. RESULTS: Steroid withdrawal could be safely achieved in low immunological risk recipients with IL2 receptor antibody induction. The incidence of biopsy-proven acute rejection was 15.1% in the low-risk and 13.9% in the high-risk group (including sub-clinical rejection detected at protocol biopsy). One- year graft survival was 93.3% and patient survival 98.5% in the low-risk group, and 97.3 and 100% respectively in the high-risk group. Graft function was similar in each group at 1 year (mean eGFR 61.2 ± 23.4 mL/min low-risk and 64.6 ± 19.2 mL/min high-risk). CONCLUSIONS: Immunosuppression regimen comprising basiliximab induction, tacrolimus, MMF and prednisolone with early steroid withdrawal in low risk patients and MMF withdrawal in high risk patients following a normal 3-month protocol biopsy is effective in limiting acute rejection episodes and produces excellent rates of patient survival, graft function and complications. BioMed Central 2020-03-11 /pmc/articles/PMC7065371/ /pubmed/32160893 http://dx.doi.org/10.1186/s12882-020-01739-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Phanish, Mysore K.
Hull, Richard P.
Andrews, Peter A.
Popoola, Joyce
Kingdon, Edward J.
MacPhee, Iain A. M.
Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title_full Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title_fullStr Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title_full_unstemmed Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title_short Immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
title_sort immunological risk stratification and tailored minimisation of immunosuppression in renal transplant recipients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065371/
https://www.ncbi.nlm.nih.gov/pubmed/32160893
http://dx.doi.org/10.1186/s12882-020-01739-3
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