An understanding of how T cell memory is maintained is crucial for the rati
onal design of vaccines. Memory T tells were shown to persist indefinitely
in major histocompatibility complex (MHC) class I-deficient mice and retain
ed the ability to make rapid cytokine responses upon reencounter with antig
en. In addition, memory CD8 T cells, unlike naive cells, divided without MH
C-T cell receptor interactions. This "homeostatic" proliferation is Likely
to be important in maintaining memory T cell numbers in the periphery. Thus
, after naive CD8 T cells differentiate into memory cells, they evolve an M
HC class I-independent "life-style" and do not require further stimulation
with specific or cross-reactive antigen for their maintenance.