To investigate the role of gamma delta T cells in human heart transpla
ntation, Fee searched for this T cell population in endomyocardial bio
psies as well as in T cell lines and clones derived from graft-infiltr
ating lymphocytes. The number of gamma delta T cells in endomyocardial
biopsies from transplanted patients (n=55) was mostly low and did not
differ significantly from nontransplanted patients (n=21). Moreover,
there was no association of gamma delta T cell distribution with rejec
tion status or with time posttransplantation. Graft-derived T cell lin
es were established in the presence of autologous feeder cells and rec
ombinant interleukin-2 to favor the growth of in vivo-activated T cell
s. Twenty T cell lines analyzed by flow cytometry showed low percentag
es of gamma delta T cells, and we were unable to obtain gamma delta T
cell clones for functional studies. These results show that gamma delt
a T cells are poorly expressed on human heart allograft infiltrates an
d indicate that, when present, they are not activated in the graft. Ou
r data suggest that gamma delta T cells do not have a major role in hu
man heart rejection.