The antigen specificity of T lymphocytes is dictated solely by the T cell r
eceptor (TC R) a and P chains. Consequently, genetic transfer of TCR chains
may be an appealing strategy with which to impose a desirable virus- or tu
mor-antigen specificity onto cytotoxic or helper T cell populations. We des
cribe here the genetic introduction of a virus-specific TCR into peripheral
T cells in a mouse model system. These experiments showed that T cells red
irected by TCR gene transfer expanded upon viral infection of mice and effi
ciently homed to effector sites. In this setting,TCR gene transfer was not
associated with any significant autoimmune pathology. In addition, small nu
mbers of TCR-transduced T cells promoted the rejection of antigen-expressin
g tumors in vivo. These data suggest that the redirection of T cells by TCR
gene transfer is a viable strategy for the rapid induction of virus- or tu
mor-specific immunity.