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* Department of Microbiology and Immunology and Cooperative Research Center for Vaccine Technology, University of Melbourne, Parkville, Victoria, Melbourne, Australia; and
Department of Cell Biology and Immunology, Vrije Universiteit, Amsterdam, The Netherlands
Salmonella are intracellular bacterial pathogens
that reside and replicate inside macrophages, and attenuated strains of
Salmonella typhimurium can be used to
deliver heterologous Ags for MHC class I and/or MHC class II-restricted
presentation. Recently, it was shown that invasion of macrophages by
S. typhimurium may result in the death of
host macrophages via a mechanism harboring features of apoptotic and
necrotic cell death. However, it is unknown whether this
bacterial-induced host cell death affects immunity. In addition, it has
been hypothesized that macrophage death following infection with
S. typhimurium and subsequent uptake of
apoptotic cells by APC are fundamental to the induction of CTL
responses. In this study we investigated the in vivo induction of
Ag-specific CD8+ T lymphocyte responses and compared
CD8+ T lymphocyte responses elicited with S.
typhimurium strains carrying a mutation in their invA
gene, and therefore an inability to induce Salmonella
pathogenicity island 1 (SPI-1)-mediated macrophage death, with
responses elicited by an attenuated
aroAD strain.
Ag-specific CD8+ T lymphocyte responses were analyzed using
IFN-
ELISPOT, tetramer binding, and in vivo and in vitro CTL assays.
Our results showed that
aroAD and
aroAD
invA induced comparable levels
of Ag-specific CD8+ T lymphocyte responses as well as
protective, Ag-specific B and CD4+ T lymphocyte immunity.
Furthermore, experiments in macrophage-depleted mice showed that
CD8+ T lymphocyte responses were effectively induced in the
absence of macrophages. Together, our results imply that in this
infection model, SPI-1-mediated cell death does not affect the
immunological defense response and is not important for the induction
of CD8+ T lymphocyte responses.
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