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Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation

Accelerated thymic involution is a main feature of end-stage renal disease (ESRD)-associated immune senescence. Recent evidences suggest that ESRD-associated immune senescence is associated with adverse outcomes in dialysis patients. However, no study focused on the association between pre-transplan...

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Autores principales: Courivaud, Cécile, Bamoulid, Jamal, Crepin, Thomas, Gaiffe, Emilie, Laheurte, Caroline, Saas, Philippe, Ducloux, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438875/
https://www.ncbi.nlm.nih.gov/pubmed/32903778
http://dx.doi.org/10.3389/fimmu.2020.01653
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author Courivaud, Cécile
Bamoulid, Jamal
Crepin, Thomas
Gaiffe, Emilie
Laheurte, Caroline
Saas, Philippe
Ducloux, Didier
author_facet Courivaud, Cécile
Bamoulid, Jamal
Crepin, Thomas
Gaiffe, Emilie
Laheurte, Caroline
Saas, Philippe
Ducloux, Didier
author_sort Courivaud, Cécile
collection PubMed
description Accelerated thymic involution is a main feature of end-stage renal disease (ESRD)-associated immune senescence. Recent evidences suggest that ESRD-associated immune senescence is associated with adverse outcomes in dialysis patients. However, no study focused on the association between pre-transplant thymic function and patient survival after transplantation. We conducted a prospective, multicenter study to assess whether pre-transplant thymic function measured by recent thymic emigrants (RTE) may predict death after first kidney transplantation. Results were tested in a validation cohort. Nine hundred and sixty-seven incident kidney transplant recipients were included in the prospective study. Mean follow up was 5.1 + 2.9 years. Eighty two patients (8.5%) died during follow up. Lower RTE levels were associated with a higher risk of death (2.53; 95%CI, 1.54–4.39 for each decrease of 1 log in RTE; p < 0.001). Cancer-related death was particularly increased in patients with low RTE levels (4.23; 95%CI, 1.43–12.13; p = 0.007). One hundred and thirty-six patients having received a first kidney transplantation were included in the validation cohort. Lower TREC levels were associated with higher risk of death (1.90; 95%CI, 1.11–3.51 for each decrease of 1 log in RTE; p = 0.025). RTE were not associated with death-censored graft loss. Pre-transplant thymic function is strongly associated with death after transplantation. Attempt to reverse ESRD-related thymic loss may prevent premature death.
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spelling pubmed-74388752020-09-03 Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation Courivaud, Cécile Bamoulid, Jamal Crepin, Thomas Gaiffe, Emilie Laheurte, Caroline Saas, Philippe Ducloux, Didier Front Immunol Immunology Accelerated thymic involution is a main feature of end-stage renal disease (ESRD)-associated immune senescence. Recent evidences suggest that ESRD-associated immune senescence is associated with adverse outcomes in dialysis patients. However, no study focused on the association between pre-transplant thymic function and patient survival after transplantation. We conducted a prospective, multicenter study to assess whether pre-transplant thymic function measured by recent thymic emigrants (RTE) may predict death after first kidney transplantation. Results were tested in a validation cohort. Nine hundred and sixty-seven incident kidney transplant recipients were included in the prospective study. Mean follow up was 5.1 + 2.9 years. Eighty two patients (8.5%) died during follow up. Lower RTE levels were associated with a higher risk of death (2.53; 95%CI, 1.54–4.39 for each decrease of 1 log in RTE; p < 0.001). Cancer-related death was particularly increased in patients with low RTE levels (4.23; 95%CI, 1.43–12.13; p = 0.007). One hundred and thirty-six patients having received a first kidney transplantation were included in the validation cohort. Lower TREC levels were associated with higher risk of death (1.90; 95%CI, 1.11–3.51 for each decrease of 1 log in RTE; p = 0.025). RTE were not associated with death-censored graft loss. Pre-transplant thymic function is strongly associated with death after transplantation. Attempt to reverse ESRD-related thymic loss may prevent premature death. Frontiers Media S.A. 2020-07-31 /pmc/articles/PMC7438875/ /pubmed/32903778 http://dx.doi.org/10.3389/fimmu.2020.01653 Text en Copyright © 2020 Courivaud, Bamoulid, Crepin, Gaiffe, Laheurte, Saas and Ducloux. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Courivaud, Cécile
Bamoulid, Jamal
Crepin, Thomas
Gaiffe, Emilie
Laheurte, Caroline
Saas, Philippe
Ducloux, Didier
Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title_full Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title_fullStr Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title_full_unstemmed Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title_short Pre-transplant Thymic Function Predicts Is Associated With Patient Death After Kidney Transplantation
title_sort pre-transplant thymic function predicts is associated with patient death after kidney transplantation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438875/
https://www.ncbi.nlm.nih.gov/pubmed/32903778
http://dx.doi.org/10.3389/fimmu.2020.01653
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