Unique molecular changes in kidney allografts after simultaneous liver-kidney compared with solitary kidney transplantation
- PMID: 28233612
- DOI: 10.1016/j.kint.2016.12.016
Unique molecular changes in kidney allografts after simultaneous liver-kidney compared with solitary kidney transplantation
Abstract
Kidney allografts transplanted simultaneously with liver allografts from the same donor are known to be immunologically privileged. This is especially evident in recipients with high levels of donor-specific anti-HLA antibodies. Here we investigated the mechanisms of liver's protective impact using gene expression in the kidney allograft. Select solitary kidney transplant or simultaneous liver-kidney transplant recipients were retrospectively reviewed and separated into four groups: 16 cross-match negative kidney transplants, 15 cross-match positive kidney transplants, 12 cross-match negative simultaneous liver-kidney transplants, and nine cross-match-positive simultaneous liver-kidney transplants. Surveillance biopsies of cross-match-positive kidney transplants had increased expression of genes associated with donor-specific antigens, inflammation, and endothelial cell activation compared to cross-match-negative kidney transplants. These changes were not found in cross-match-positive simultaneous liver-kidney transplant biopsies when compared to cross-match-negative simultaneous liver-kidney transplants. In addition, simultaneously transplanting a liver markedly increased renal expression of genes associated with tissue integrity/metabolism, regardless of the cross-match status. While the expression of inflammatory gene sets in cross-match-positive simultaneous liver-kidney transplants was not completely reduced to the level of cross-match-negative kidney transplants, the downstream effects of donor-specific anti-HLA antibodies were blocked. Thus, simultaneous liver-kidney transplants can have a profound impact on the kidney allograft, not only by decreasing inflammation and avoiding endothelial cell activation in cross-match-positive recipients, but also by increasing processes associated with tissue integrity/metabolism by unknown mechanisms.
Keywords: alloimmunity; gene expression; kidney transplantation; liver transplantation; rejection; simultaneous liver-kidney transplantation.
Copyright © 2017 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.
Comment in
-
Simultaneous liver-kidney transplantation: shifting renal allograft gene expression from inflammation toward preservation.Kidney Int. 2017 May;91(5):1010-1013. doi: 10.1016/j.kint.2017.02.015. Kidney Int. 2017. PMID: 28407877
Similar articles
-
Revisiting the liver's role in transplant alloimmunity.World J Gastroenterol. 2019 Jul 7;25(25):3123-3135. doi: 10.3748/wjg.v25.i25.3123. World J Gastroenterol. 2019. PMID: 31333306 Free PMC article. Review.
-
Longterm renal allograft survival after sequential liver-kidney transplantation from a single living donor.Liver Transpl. 2017 Mar;23(3):315-323. doi: 10.1002/lt.24676. Epub 2017 Feb 6. Liver Transpl. 2017. PMID: 27862900
-
Eplet mismatch analysis and allograft outcome across racially diverse groups in a pediatric transplant cohort: a single-center analysis.Pediatr Nephrol. 2020 Jan;35(1):83-94. doi: 10.1007/s00467-019-04344-1. Epub 2019 Oct 10. Pediatr Nephrol. 2020. PMID: 31599339 Free PMC article.
-
Influence of preformed donor-specific antibodies and C4d on early liver allograft function.Scand J Gastroenterol. 2013 Dec;48(12):1444-51. doi: 10.3109/00365521.2013.845795. Epub 2013 Oct 16. Scand J Gastroenterol. 2013. PMID: 24131305
-
Emphysematous pyelonephritis in renal allograft related to antibody-mediated rejection: A case report and literature review.Transpl Infect Dis. 2019 Feb;21(1):e13026. doi: 10.1111/tid.13026. Epub 2018 Dec 4. Transpl Infect Dis. 2019. PMID: 30414224 Review.
Cited by
-
Liver mesenchymal stem cells are superior inhibitors of NK cell functions through differences in their secretome compared to other mesenchymal stem cells.Front Immunol. 2022 Sep 21;13:952262. doi: 10.3389/fimmu.2022.952262. eCollection 2022. Front Immunol. 2022. PMID: 36211345 Free PMC article.
-
Human liver derived mesenchymal stromal cells ameliorate murine ischemia-induced inflammation through macrophage polarization.Front Immunol. 2024 Jul 22;15:1448092. doi: 10.3389/fimmu.2024.1448092. eCollection 2024. Front Immunol. 2024. PMID: 39104523 Free PMC article.
-
Immunology of simultaneous liver and kidney transplants with identification and prevention of rejection.Front Transplant. 2022 Nov 1;1:991546. doi: 10.3389/frtra.2022.991546. eCollection 2022. Front Transplant. 2022. PMID: 38994375 Free PMC article. Review.
-
Revisiting the liver's role in transplant alloimmunity.World J Gastroenterol. 2019 Jul 7;25(25):3123-3135. doi: 10.3748/wjg.v25.i25.3123. World J Gastroenterol. 2019. PMID: 31333306 Free PMC article. Review.
-
Burden of early hospitalization after simultaneous liver-kidney transplantation: Results from the US Multicenter SLKT Consortium.Liver Transpl. 2022 Nov;28(11):1756-1765. doi: 10.1002/lt.26523. Epub 2022 Jul 4. Liver Transpl. 2022. PMID: 35665591 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials