Abstract

Liver transplantation is an established therapy for end-stage liver diseases. Graft rejection occurs unless the recipient receives immunosuppression after transplantation. This study aimed to explore the mechanism of acute rejection of liver allografts in rats pre-treated with total body irradiation to eliminate passenger lymphocytes and to define the role of CD4(+)CD25(+) regulatory T cells in the induction of immunotolerance in the recipient. Male Lewis rats were used as donors and male DA rats were recipients. Rats were randomly assigned to the following four groups: control group, homogeneity liver transplantation group, idio-immunotolerance group and acute rejection group. After transplantation, the survival time of each group, serum alanine aminotransferase, total bilirubin levels, number of Foxp3(+)CD4(+)CD25(+) regulatory T cells, expression of glucocorticoid-induced tumor necrosis factor receptor on T cell subgroups, histopathology of the hepatic graft and spleen cytotoxic T lymphocyte lytic activity were measured. In the acute rejection group, where donors were preconditioned with total body irradiation before liver transplantation, all recipients died between day 17 and day 21. On day 14, serum alanine aminotransferase increased significantly to (459.2±76.9) U L(-1), total bilirubin increased to (124.1±33.7) μmol L(-1) (P<0.05) and the ratio of Foxp3(+)CD4(+)CD25(+) regulatory T cells decreased significantly to 1.50%±0.50% (P<0.05) compared with the other groups. Analysis of the T cell subpopulations in the acute rejection group varied from the other groups. Histological analysis showed typical changes of acute rejection in the acute rejection group only. Preconditioning of the donors with total body irradiation eliminated passenger lymphocytes of the liver graft, and thus affected the course of tolerance and induced acute rejection after liver transplantation.

Highlights

  • In end-stage liver disease, liver transplantation is often performed

  • This study aimed to explore the mechanism of acute rejection of liver allografts in rats pre-treated with total body irradiation to eliminate passenger lymphocytes and to define the role of CD4+CD25+ regulatory T cells in the induction of immunotolerance in the recipient

  • 2.2 Increased levels of alanine transaminase (ALT) and total bilirubin (TB) were maintained in the acute rejection group

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Summary

Introduction

In end-stage liver disease, liver transplantation is often performed. One disadvantage of transplantation is that graft rejection occurs unless the recipient receives immunosuppression after transplantation. The aims of this study were to investigate the mechanism of acute rejection induced by elimination of passenger lymphocytes in the donor liver grafts by TBI, to define the role of CD4+CD25+ regulatory T cells (Tregs) in the induction of immunotolerance after liver transplantation, and to explore the mechanism of the immunologically privileged status of the liver. Expression of glucocorticoid-induced tumor necrosis factor (TNF) receptor (GITR), a TNF receptor superfamily member, provides costimulatory signals that activate T cells and counteracts the suppressive activity of CD4+CD25+ Tregs. This induces an up-regulation of the immune response, intensifying the generation and development of autoimmune diseases [4,5]. We studied the mechanism of TBI-induced acute rejection of rat liver transplantation and the role of CD4+CD25+ Tregs in inducing immune tolerance

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