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High frequency of central memory regulatory T cells allows detection of liver recipients at risk of early acute rejection within the first month after transplantation.

Authors :
Boix-Giner, Francisco
Millan, Olga
Segundo, David San
Muñoz-Cacho, Pedro
Mancebo, Esther
Llorente, Santiago
Rafael-Valdivia, Lourdes
Rimola, Antoni
Fábrega, Emilio
Mrowiec, Anna
Allende, Luis
Minguela, Alfredo
Bolarín, Jose M.
Paz-Artal, Estela
López-Hoyos, Marcos
Brunet, Mercé
Muro, Manuel
Source :
International Immunology. Feb2016, Vol. 28 Issue 2, p55-64. 10p.
Publication Year :
2016

Abstract

Several studies have analyzed the potential of T regulatory cells (Treg cells) as biomarkers of acute rejection (AR). The aim of the present multicenter study was to correlate the percentage of peripheral Treg cells in liver graft recipients drawn at baseline up to 12 months after transplantation with the presence of AR. The percentage of central memory (cm) Treg cells (CD4+CD25highCD45RO+CD62L+) was monitored at pre-transplant and at 1 and 2 weeks, and 1, 2, 3 and 6 months and 1 year posttransplantation. The same validation standard operating procedures were used in all participating centers. Fifteen patients developed AR (23.4%). Hepatitis C virus recurrence was observed in 16 recipients, who displayed low peripheral blood cmTreg levels compared with patients who did not. A steady increase of cmTregs was observed during the first month after transplantation with statistically significant differences between AR and non-AR patients. The high frequency of memory Treg cells allowed us to monitor rejection episodes during the first month post-transplantation. On the basis of these data, we developed a prediction model for assessing risk of AR that can provide clinicians with useful information for managing patients individually and customizing immunosuppressive therapies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09538178
Volume :
28
Issue :
2
Database :
Academic Search Index
Journal :
International Immunology
Publication Type :
Academic Journal
Accession number :
112590738
Full Text :
https://doi.org/10.1093/intimm/dxv048