Danielle F.
Eytan1, T Kevin Hitchens1, Qing Ye1, Yijen
L. Wu1, Chien Ho1
1Pittsburgh
Abundant
macrophage infiltration is observed in cardiac allograft rejection, yet their
contribution to the rejection process and the tissue damage that results
remains unclear. Here we investigated the role these cells play in our rat
model of acute cardiac rejection by selectively depleting circulating
macrophages using liposomal-clodronate. We used T2*-weighted imaging to
detect immune-cell infiltration at sites of rejection by monitoring the
accumulation of iron oxide-labeled cells, and cardiac cine-tagging to detect
regional myocardial function loss. Our results indicate that macrophages
contribute to tissue damage during acute rejection, and that their depletion
may attenuate the damaging effects of rejection in rat cardiac allografts.