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Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients

BACKGROUND: For the growing numbers of older transplant patients, increased incidence of infection and death compared with younger patients may limit the many benefits provided by transplantation. However, little is known about age-associated immune dysfunction in the older transplant recipient. MET...

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Autores principales: Schaenman, Joanna M., Rossetti, Maura, Lum, Erik, Abdalla, Basmah, Bunnapradist, Suphamai, Pham, Thu-Phuong, Danovitch, Gabriel, Reed, Elaine F., Cole, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445656/
https://www.ncbi.nlm.nih.gov/pubmed/30993190
http://dx.doi.org/10.1097/TXD.0000000000000870
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author Schaenman, Joanna M.
Rossetti, Maura
Lum, Erik
Abdalla, Basmah
Bunnapradist, Suphamai
Pham, Thu-Phuong
Danovitch, Gabriel
Reed, Elaine F.
Cole, Steve
author_facet Schaenman, Joanna M.
Rossetti, Maura
Lum, Erik
Abdalla, Basmah
Bunnapradist, Suphamai
Pham, Thu-Phuong
Danovitch, Gabriel
Reed, Elaine F.
Cole, Steve
author_sort Schaenman, Joanna M.
collection PubMed
description BACKGROUND: For the growing numbers of older transplant patients, increased incidence of infection and death compared with younger patients may limit the many benefits provided by transplantation. However, little is known about age-associated immune dysfunction in the older transplant recipient. METHODS: A cohort of 60 kidney transplant recipients, 23 older (≥ 60y) and 37 younger (30-59y), matched on antithymocyte induction and donor type (living vs deceased) was evaluated. Gene expression in peripheral blood mononuclear cells 3 months after kidney transplantation was analyzed to compare differences between older and younger patients. RESULTS: Proinflammatory genes were upregulated in older kidney transplant patients, including cytokines IL1-β and IL-6. Downregulated genes were associated with B-cell and T-cell function, including CCR7 and CD27. Analysis of predicted transcription factor binding suggested an increase in proinflammatory transcription factor CCAAT/enhancer binding protein β-binding sites in older patients, whereas interferon regulatory factor 2 transcription factor binding sites were less prevalent. CONCLUSIONS: Older kidney transplant recipients exhibited multiple differences in gene expression compared with younger patients, with upregulation of proinflammatory genes and downregulation of adaptive immune response genes. These findings may explain the mechanism of increased vulnerability to infection and malignancy observed in older transplant patients.
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spelling pubmed-64456562019-04-16 Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients Schaenman, Joanna M. Rossetti, Maura Lum, Erik Abdalla, Basmah Bunnapradist, Suphamai Pham, Thu-Phuong Danovitch, Gabriel Reed, Elaine F. Cole, Steve Transplant Direct Kidney Transplantation BACKGROUND: For the growing numbers of older transplant patients, increased incidence of infection and death compared with younger patients may limit the many benefits provided by transplantation. However, little is known about age-associated immune dysfunction in the older transplant recipient. METHODS: A cohort of 60 kidney transplant recipients, 23 older (≥ 60y) and 37 younger (30-59y), matched on antithymocyte induction and donor type (living vs deceased) was evaluated. Gene expression in peripheral blood mononuclear cells 3 months after kidney transplantation was analyzed to compare differences between older and younger patients. RESULTS: Proinflammatory genes were upregulated in older kidney transplant patients, including cytokines IL1-β and IL-6. Downregulated genes were associated with B-cell and T-cell function, including CCR7 and CD27. Analysis of predicted transcription factor binding suggested an increase in proinflammatory transcription factor CCAAT/enhancer binding protein β-binding sites in older patients, whereas interferon regulatory factor 2 transcription factor binding sites were less prevalent. CONCLUSIONS: Older kidney transplant recipients exhibited multiple differences in gene expression compared with younger patients, with upregulation of proinflammatory genes and downregulation of adaptive immune response genes. These findings may explain the mechanism of increased vulnerability to infection and malignancy observed in older transplant patients. Lippincott Williams & Wilkins 2019-03-04 /pmc/articles/PMC6445656/ /pubmed/30993190 http://dx.doi.org/10.1097/TXD.0000000000000870 Text en Copyright © 2019 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. 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) (http://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
Schaenman, Joanna M.
Rossetti, Maura
Lum, Erik
Abdalla, Basmah
Bunnapradist, Suphamai
Pham, Thu-Phuong
Danovitch, Gabriel
Reed, Elaine F.
Cole, Steve
Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title_full Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title_fullStr Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title_full_unstemmed Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title_short Differences in Gene Expression in Older Compared With Younger Kidney Transplant Recipients
title_sort differences in gene expression in older compared with younger kidney transplant recipients
topic Kidney Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445656/
https://www.ncbi.nlm.nih.gov/pubmed/30993190
http://dx.doi.org/10.1097/TXD.0000000000000870
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