Normal human T lymphocytes, activated in vitro and cultured in the continuous presence of the growth factor interleukin 2 (IL2), have a limited proliferative potential. Senescent T cell cultures will not proliferate, even if restimulated by the original allogeneic stimulator cells. However, we have now observed that such restimulation induces an increase in the percentage of cells expressing the 55 kDa chain of the IL2 receptor (IL2R alpha, CD25) without any associated increase in cell number. A younger culture, which showed a comparable increase in CD25, underwent two population doublings in the same time period after restimulation. The senescent cultures, (primarily of the CD8+, cytotoxic/suppressor, phenotype), were also found to be highly potent and specific effector cells in a 51chromium release assay for cytolytic activity. Furthermore, senescent cultures maintain the surface phenotype of memory T cells. These findings demonstrate that while senescent T cells are unable to proliferate in response to restimulation or to IL2, they are able to recognize the foreign stimulator cells and to initiate an otherwise normal T cell response. Our results lend support to the hypothesis that in vitro senescence is not associated with a generalized decline in functional activity in a differentiated cell type, but with a specific event which limits cell division. Thus, the long term T lymphocyte culture system will be useful for studying the mechanism by which proliferation is blocked in these, apparently, post-mitotic cells.