Whether CD8 T cell memory exists outside secondary lymphoid organs is uncle
ar. Using an adoptive transfer system that enables tracking of OVA-specific
CD8 T cells, we explored the antigenic requirements for inducing CD8 T cel
l memory and identified intestinal mucosa memory cells. Although systemic i
mmunization with soluble OVA induced clonal expansion, memory CD8 cells wer
e not produced. In contrast, infection with virus-encoding OVA induced memo
ry CD8 cells in the periphery and the lamina propria and intraepithelial co
mpartments of the intestinal mucosa, Mucosal memory cells expressed a disti
nct array of adhesion molecules as compared with secondary lymphoid memory
cells, suggesting that there may be separate mucosal and systemic memory po
ols. Mucosal CD8 memory cells rapidly produced IFN-gamma after Ag stimulati
on, Reactivation of memory cells by Ag feeding resulted in increased cell s
ize and up-regulation of CD28 and CD11c, CD8 mucosal memory cells exhibited
ex vivo lytic activity that was up-regulated dramatically following Ag ree
ncounter in vivo, Interestingly, reactivation of memory cells did not requi
re CD28-mediated costimulation, The ability of the intestinal mucosa to mai
ntain CD8 memory cells provides a potential mechanism for effective mucosal
vaccination.