Unique molecular changes in kidney allografts after simultaneous liver-kidney compared with solitary kidney transplantation
Kidney International, ISSN: 0085-2538, Vol: 91, Issue: 5, Page: 1193-1202
2017
- 56Citations
- 35Captures
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Metrics Details
- Citations56
- Citation Indexes56
- 56
- CrossRef25
- Captures35
- Readers35
- 35
Article Description
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.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0085253816307591; http://dx.doi.org/10.1016/j.kint.2016.12.016; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85013399300&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28233612; https://linkinghub.elsevier.com/retrieve/pii/S0085253816307591
Elsevier BV
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