Engagement of inhibitory natural killer (NK) cell receptors for MHC class I
molecules (NKR) can impair NK-cell activation programs. Inhibitory NKR thu
s confer to NK cells the capacity to discriminate between MHC class I+ and
MHC class I- target cells, and are therefore involved in the control of NK-
cell tolerance to self, as well as in the elimination of MHC class I- distr
essed cells by NK cells. In human and mouse, a subset of alpha beta T cells
also express inhibitory NKR at their surface, but the biological function
of inhibitory NKR on T cells remains to be precisely elucidated. We refer t
o these cells as T memory type 1 (Tm1) cells, and review here the phenotypi
c and functional features of this subset of memory-phenotype CD8(+) alpha b
eta T cells. in vitro studies suggest that inhibitory NKR are involved in t
he peripheral control of T-cell self-tolerance. In vitro and in vivo analys
is have revealed a novel biological function for inhibitory NKR when expres
sed on T cells. Indeed, engagement of inhibitory NKR on T cells provides th
em with survival signals against activation-induced cell death. Thus, sensi
ng of self-MHC class I molecules by inhibitory NKR displayed on alpha beta
T cells leads to the in vivo accumulation of Tm 1 cells.