HLA-C is a non-classical MHC class I molecule expressed at the fete/materna
l interface where it plays a role in materno-fetal tolerance by inhibiting
NK cells. Expression of killing inhibitory receptors capable of interacting
with HLA-G on T lymphocytes led us to hypothesize that HLA-G molecules cou
ld also modulate T cell responses, analyzed here in the context of the allo
geneic proliferative response. Using LCL-HLA-G transfectants as stimulators
of T cells present among peripheral mononuclear cells and K562-HLA-G1 tran
sfectants as inhibitors in a classical mixed lymphocyte reaction, we showed
that HLA-G is able to inhibit T cell allo-proliferation. These findings pr
ovide new insight into the role of HLA-G in preventing allograft rejection.
(C) 1999 Elsevier Science Ireland Ltd. All rights reserved.