Prolongation of alloskin graft survival by catalytic scavengers of reactive oxygen species

Cell Immunol. 2006 Jun;241(2):59-65. doi: 10.1016/j.cellimm.2006.06.009. Epub 2006 Sep 12.

Abstract

We tested the effects of salen manganese (Salen-Mn) complexes, which are scavengers of reactive oxygen species exhibiting superoxide dismutase and catalase activities on the rejection of and alloresponse to fully allogeneic skin grafts in mice. We showed that pre-transplant treatment of C57Bl/6 donor skin or of BALB/c recipients with Salen-Mn complexes significantly delayed allograft rejection. ELISPOT analysis of alloimmune response of treated mice revealed a significant reduction of the frequency of type 1 cytokine (pro-inflammatory) producing T-cells, while the number of activated T-cells producing type 2 cytokines was elevated. In addition, anti-oxidative treatment of graft recipients resulted in a profound inhibition of their donor-specific cytotoxic T-cell response. Our results indicate that salen manganese complexes mediate their effect on graft rejection both by reducing the susceptibility of graft tissue to ROS-mediated injury and by exerting an anti-inflammatory effect in recipients.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catalase / metabolism
  • Catalysis / drug effects
  • Cytokines / biosynthesis
  • Cytotoxicity, Immunologic / drug effects
  • Female
  • Free Radical Scavengers / pharmacology*
  • Graft Rejection / immunology
  • Graft Survival / drug effects*
  • Graft Survival / immunology*
  • In Vitro Techniques
  • Inflammation Mediators / immunology
  • Manganese / pharmacology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Models, Immunological
  • Reactive Oxygen Species / metabolism*
  • Skin Transplantation / immunology*
  • Superoxide Dismutase / metabolism
  • T-Lymphocytes, Cytotoxic / drug effects
  • Transplantation, Homologous

Substances

  • Cytokines
  • Free Radical Scavengers
  • Inflammation Mediators
  • Reactive Oxygen Species
  • Manganese
  • Catalase
  • Superoxide Dismutase