The Traf-linked tumor necrosis factor receptor family member CD27 is known
as a T cell costimulatory molecule. We generated CD27(-/-) mice and found t
hat CD27 makes essential contributions to mature CD4(+) and CD8(+) T cell f
unction: CD27 supported antigen-specific expansion (but not effector cell m
aturation) of naive T cells, independent of the cell cycle-promoting activi
ties of CD28 and interleukin 2. Primary CD4(+) and CD8(+) T cell responses
to influenza virus were impaired in CD27(-/-) mice. Effects of deleting the
gene encoding CD27 were most profound on T cell memory, reflected by delay
ed response kinetics and reduction of CD8(+) virus-specific T cell numbers
to the level seen in the primary response. This demonstrates the requiremen
t for a costimulatory receptor in the generation of T cell memory.