Interferon- γ derived from cytotoxic lymphocytes directly enhances their motility and cytotoxicity

Interferon gamma (IFN γ ) is a key moderator of cell-mediated immunity with diverse, mainly pro-inflammatory actions on immunocytes and target tissue. Recent studies have shown it may enhance anti-tumor and antiviral effects of CD8 T cells. Here we investigate the mechanisms by which IFN γ mediates CD8 T-cell cytotoxic function. We show that in vivo , antigen-specific CD8 T cells that produce INF γ are necessary to effect rejection of skin grafts expressing OVA as a transgene in keratinocytes. The ability of CD8 T cells to produce IFN γ enhanced their ability to migrate to the site of antigen-presenting skin cells. By in vivo imaging, we show that CTL motility, particularly speed, during graft rejection was enhanced by locally available IFN γ . We then used a reductionist two-cell model of CTL effectors and keratinocyte targets to investigate the effects of locally available (paracrine) and CTL-producing (autocrine) IFN γ on the motility behavior and killing ability of the CTL. Using live-cell imaging by prolonged time-lapse microscopy of primary effector CD8 T cells and antigen-expressing primary keratinocyte targets, we show that CD8 T-cell cytotoxic function and motility is enhanced by locally available IFN γ . Conversely, deprivation of either autocrine or paracrine IFN γ , or blockade of IFN γ signaling to CTL markedly reduced their cytotoxic function, their kinematics, and effector cell survival. We conclude that in vitro and in vivo, autocrine production of IFN γ by CTL enhances their motility and promotes killing of primary target keratinocytes. The absolute need for local IFN γ to enable cytotoxic CD8 T-cell function is of significance for immunotherapy for chronic viral infection and for cancer.