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Department of Biology, University of North Carolina, Charlotte, NC 28223
Expression of high affinity IL-12 receptors is required for
IL-12-mediated IFN-
production. Activation of this pathway has been
shown to be critical in generating optimal cell-mediated immunity.
Therefore, increased IL-12 receptor expression might be expected in the
host response after infection by an intracellular bacterial pathogen.
In the present study, we have made the surprising discovery that
infection with Salmonella results in an early reduction
of high affinity IL-12 receptor expression and activation. After oral
inoculation with Salmonella, the level of mRNA
expression encoding IL-12 receptor ß2 (IL-12Rß2) subunit was
diminished 12 h postinfection in the mesenteric lymph nodes and
subsequently in the spleen. Furthermore, decreased IL-12Rß2 mRNA
expression was observed in CD4+ T lymphocytes isolated from
the mesenteric lymph nodes and spleens of infected mice. Attenuated
IL-12Rß2 mRNA expression correlated with reduced receptor signaling,
as demonstrated by reduced IL-12-induced STAT4 phosphorylation in
enriched T lymphocytes isolated from the mesenteric lymph nodes and
spleens of Salmonella-infected mice. These in vivo
results were substantiated with an in vitro model system. In this model
system, T lymphocytes cocultured with
Salmonella-infected macrophages expressed less
IL-12Rß2 mRNA. The cocultured T cells were also less responsive to
IL-12 as assessed by reduced phosphorylation of STAT4 and limited
IFN-
secretion. Together, these studies suggest that
Salmonella can limit an optimal host immune response by
reducing the expression and activity of high affinity IL-12
receptors.
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