A potent role for memory CD8(+) T cells in heterologous immunity was shown
with a respiratory mucosal model of viral infection. Memory CD8(+) T cells
generated after lymphocytic choriomeningitis virus (LCMV) infection were fu
nctionally activated in vivo to produce interferon-gamma (IFN-gamma) during
acute infection with vaccinia virus (VV). Some of these antigen-specific m
emory cells selectively expanded in number, which resulted in modulation of
the original LCMV-specific T cell repertoire. In addition, there was an or
gan-selective compartmental redistribution of these LCMV-specific T cells d
uring VV infection. The presence of these LCMV-specific memory T cells corr
elated with enhanced VV clearance, decreased mortality and marked changes i
n lung immunopathology. Thus, the participation of pre-existing memory T ce
lls specific to unrelated agents can alter the dynamics of mucosal immunity
and disease course in response to a pathogen.