Scientific publications

Differential profile of activated regulatory T cell subsets and microRNAs in tolerant liver transplant recipients

Revilla-Nuin B (1), de Bejar Á (2), Martínez-Alarcón L (1), Herrero JI (3), Martínez-Cáceres CM (1), Ramírez P (1,4), Baroja-Mazo A (1), Pons JA (1,4).

(1) Biomedical Research Institute of Murcia, University Clinical Hospital "Virgen de la Arrixaca," University of Murcia, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Murcia, Spain.
(2) Clinical Laboratory Unit, Hospital General Universitario Santa Lucía, Cartagena, Spain.
(3) Liver Unit, Clínica Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra, Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas, Pamplona, Spain.
(4) Division of Gastroenterology and Hepatology and Liver Transpant Unit, University Hospital Virgen de la Arrixaca, Murcia, Spain.

Magazine: Liver Transplantation

Date: Jul 3, 2017



Regulatory T cells (Tregs) play a potential role in operational tolerance in liver transplantation (LT) patients, and microRNAs (miRNAs) are known to be involved in immunological responses and tolerance.

Thus, we analyzed the implication of different peripheral blood Treg subsets and miRNAs on LT tolerance in 24 tolerant (Tol) and 23 non-tolerant (non-Tol) LT recipients by cellular, genetic, and epigenetic approximation. Non-Tol patients had a lower demethylation rate of the forkhead box P3 (FOXP3) regulatory T cell-specific demethylated region (TSDR) than Tol patients that correlated with the frequency of circulating Tregs.

Tol patients presented a different signature of Treg subset markers compared with non-Tol patients with increased expression of HELIOS and FOXP3 and a higher proportion of latency-associated peptide (LAP)+ Tregs and CD45RA- human leukocyte antigen D related (HLA-DR)+ activated effector-memory Tregs.

The expression of miR95, miR24, miR31, miR146a, and miR155 was higher in Tol than in non-Tol patients and was positively correlated with activated Treg markers. In conclusion, these data suggest that activated effector-memory Tregs and a TSDR-demethylation state of Tregs may play a role in the complex system of regulation of LT tolerance. In addition, we describe a set of miRNAs differentially expressed in human LT Tol patients providing suggestive evidence that miRNAs are implied in the preservation of self-tolerance as mediated by Tregs. Liver Transplantation 23 933-945 2017 AASLD.

CITATION  Liver Transpl. 2017 Jul;23(7):933-945. doi: 10.1002/lt.24691.



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