The mechanisms responsible for the generation and maintenance of T cell mem
ory are unclear. In this study, we tested the role of IL-2 in allospecific
CD8(+) T cell memory by analyzing the long-term survival, phenotype, and fu
nctional characteristics of IL-2-replete (IL-2(+/+)) and IL-2-deficient (IL
-2(-/-)) CD8(+) TCR-transgenic lymphocytes in an adoptive transfer model. W
e found that IL-2 is not essential for the in vivo generation, maintenance,
or recall response of CD8(+) memory T cells. However, IL-2 increased the s
ize of the CD8(+) memory pool if present at the time of initial T cell acti
vation but reduced the size of the pool if present during memory maintenanc
e by inhibiting the proliferation of CD8(+) memory T cells. Thus, IL-2-base
d vaccine strategies or immunosuppressive regimens that target IL-2 should
take into account the divergent roles of IL-2 in CD8(+) T cell immunity.