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Peripheral phenotype and gene expression profiles of combined liver-kidney transplant patients.

Authors :
Dumontet E
Danger R
Vagefi PA
Londoño MC
Pallier A
Lozano JJ
Giral M
Degauque N
Soulillou JP
Martínez-Llordella M
Lee H
Latournerie M
Boudjema K
Dulong J
Tarte K
Sanchez-Fueyo A
Feng S
Brouard S
Conchon S
Source :
Liver international : official journal of the International Association for the Study of the Liver [Liver Int] 2016 Mar; Vol. 36 (3), pp. 401-9. Date of Electronic Publication: 2015 Aug 08.
Publication Year :
2016

Abstract

Background and Aims: The beneficial effect of one graft on another has been reported in combined transplantation but the associated mechanisms and biological influence of each graft have not yet been established.<br />Methods: In multiple analyses, we explored the PBMC phenotype and signature of 45 immune-related messenger RNAs and 754 microRNAs from a total of 235 patients, including combined liver-kidney transplant recipients (CLK), patients with a liver (L-STA) or kidney (K-STA) graft only under classical immunosuppression and patients with tolerated liver (L-TOL) or kidney grafts (K-TOL).<br />Results: CLK show an intermediary phenotype with a higher percentage of peripheral CD19(+) CD24(+) CD38(Low) memory B cells and Helios(+) Treg cells, two features associated with tolerance profiles, compared to L-STA and K-STA (P < 0.05, P < 0.01). Very few miRNA were significantly differentially expressed in CLK vs. K-STA and even fewer when compared to L-STA (35 and 8, P < 0.05). Finally, CLK are predicted to share common miRNA targets with K-TOL and even more with L-TOL (344 and 411, P = 0.005). Altogether CLK display an intermediary phenotype and gene profile, which is closer to that of liver transplant patients, with possible similarities with the profiles of tolerant patients.<br />Conclusion: These data suggest that CLK patients show the immunological influence of both allografts with liver having a greater influence.<br /> (© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1478-3231
Volume :
36
Issue :
3
Database :
MEDLINE
Journal :
Liver international : official journal of the International Association for the Study of the Liver
Publication Type :
Academic Journal
Accession number :
26193627
Full Text :
https://doi.org/10.1111/liv.12917