Cd8 T cell-mediated rejection of intestinal allografts is resistant to inhibition of the CD40/CD154 costimulatory pathway

Background. Disruption of the CD40/CD154 pathway inhibits rejection in numerous models. The importance of this pathway on intestinal allograft rejection was examined in this study. Methods. Intestinal grafts from B6C3F1 mice transplanted into C57BL/6 recipients were assessed histologically for rejection. Results. The monoclonal antibody to CD154, MR1, failed to inhibit rejection in wild-type mice. Similarly, CD154(-/-) recipient mice rejected intestinal allografts. MR1 did inhibit early rejection in CD8(-/-) mice, but had no effect in CD4(-/-) recipients. AU MR1-treated CD8(-/-) recipients eventually developed rejection, No benefit was observed when blockade of the CD40/CD154 pathway by MR1 was combined with blockade of the CD28/B7 pathway by mCTLA4Ig. Conclusions. These data suggest that CD4(+) T cells mediating intestinal allograft rejection may be more dependent upon the CD40/CD154 pathway than CD8(+) T cells. This finding highlights the importance of identifying agents that suppress CD8(+) T cell-mediated rejection.