4.1 Article

Expression of Glucocorticoid-Induced Tumor Necrosis Factor Receptor Ligand in Rat Graft after Liver Transplantation

Journal

TRANSPLANTATION PROCEEDINGS
Volume 43, Issue 5, Pages 1971-1975

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.transproceed.2011.03.054

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Funding

  1. National Natural Science Foundation of China [30772098, 30972888, 81070374, 30801126]

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Background. Costimulation between the glucocorticoid-induced tumor necrosis factor receptor and its ligand (GITRL) breaks immunologic tolerance induced by regulatory T cells. The purpose of this research was to examine the involvement of GITRL during rat liver transplantation, the survival of which depends on interactions between regulatory T cells and Kupffer cells (KCs). Methods. Recipients were divided into 2 groups: The allograft group underwent orthotopic liver transplantation from male Lewis to Brown Norway (BN) rats and the isograft group, BN-to-BN liver transplantation. We evaluated 2-week survival rates, histologic changes, as well as serum and supernatant levels of tumor necrosis factor-alpha (TNF-alpha); GITRL, and TNF-alpha expressions in the graft, and GITRL expression by graft-derived KCs. Results. TNF-alpha levels were increased in plasma and in the supernates of KCs during allograft transplantation compared with isograft liver transplantation (P < .05). The expressions of TNF-alpha and GITRL in liver grafts were increased during acute rejection. Furthermore, the expression of GITRL on KCs derived from allografts was increased compared with isografts (P < .05). Conclusion. GITRL expression on KCs may mediate acute rejection in liver transplantation.

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