Hga. Bouwer et Dj. Hinrichs, CYTOTOXIC-T-LYMPHOCYTE RESPONSES TO EPITOPES OF LISTERIOLYSIN-O AND P60 FOLLOWING INFECTION WITH LISTERIA-MONOCYTOGENES, Infection and immunity, 64(7), 1996, pp. 2515-2522
In order to test the influence of the cell surface density of a specif
ic H2-K-d-presented epitope on the subsequent level of the cytotoxic-T
-lymphocyte (CTL) response directed against the epitope, we investigat
ed the CTL response to two secreted products of Listeria monocytogenes
from mice immunized with viable L. monocytogenes. We determined the r
esponse to the H2-K-d-presented amino acid 91 to 99 (aa91-99) immunodo
minant peptide of listeriolysin O (LLO) and to the aa217-225 immunodom
inant peptide of p60. The p60-derived peptide appears at the cell surf
ace as an H2-K-d-complexed peptide at a level sixfold higher than that
of LLO aa91-99. CTL frequency analysis of anti-LLO- or anti-p60-speci
fic CTLs from mice immunized with wild-type L. monocytogenes showed th
at the numbers of immune spleen cell-derived CTLs specific for the two
peptides were essentially equivalent. We have also found that Listeri
a-specific CTL populations lyse target cells pulsed with the p60 aa217
-225 peptide with a magnitude of the lyric response markedly less than
that for targets pulsed with the LLO aa91-99 peptide, Additionally, i
mmunization with mutants oft. monocytogenes which do not stimulate ant
i-LLO-specific CTLs does not alter the CTL frequency of anti-p60-speci
fic effector cells, with levels of anti-p60-specific CTLs similar to t
hose seen in mice immunized with wild-type L. monocytogenes. These res
ults suggest that the relative cell surface density of major histocomp
atibility complex class I-presented L. monocytogenes-derived epitopes
Is but one of the criteria which determine the magnitude of the cytoto
xic effector cell response that develops in antilisterial immunity.