Induction and maintenance of peripheral tolerance are important mechan
isms to maintain the balance of the immune system. In addition to the
deletion of T cells and their failure to respond in certain circumstan
ces, active suppression mediated by T cells or T-cell factors has been
proposed as a mechanism for maintaining peripheral tolerance(1). Howe
ver, the inability to isolate and clone regulatory T cells involved in
antigen-specific inhibition of immune responses has made it difficult
to understand the mechanisms underlying such active suppression. Here
we show that chronic activation of both human and murine CD4(+) T cel
ls in the presence of interleukin (IL)-10 gives rise to CD4(+) T-cell
clones with low proliferative capacity, producing high levels of IL-10
, low levels of IL-2 and no IL-4. These antigen-specific T-cell clones
suppress the proliferation of CD4(+) T cells in response to antigen,
and prevent colitis induced in SCID mice by pathogenic CD4(+)CD45RB(hi
gh) splenic T cells. Thus IL-10 drives the generation of a CD4(+) T-ce
ll subset, designated T regulatory cells 1 (Tr1), which suppresses ant
igen-specific immune responses and actively downregulates a pathologic
al immune response in vivo.