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Department of Microbiology, University of Pennsylvania Medical School, Philadelphia, PA 19104
Listeria monocytogenes is a facultative
intracellular bacterium that lives and grows in the cytoplasm of the
host cell. The hallmark of a listerial infection is a cell-mediated
immune response to its own secreted virulence factors. Thus, L.
monocytogenes vaccines engineered to secrete HIV proteins may
be ideal vectors for boosting cellular immune responses against HIV.
Using strains of L. monocytogenes that stably express
and secrete HIV Gag (Lm-Gag) to deliver this Ag to the immune system,
we have previously shown strong MHC class I-restricted cytotoxic T cell
responses to this protein. In this study, we examine MHC class
II-restricted T cell responses to HIV-Gag delivered by Lm-Gag. We
demonstrate the induction of CD4+ T cells that are HIV-Gag
specific and identify three epitopes in two strains of mice, BALB/c
(H-2d) and C57BL/6 (H-2b), two of which are
both H-2d and H-2b restricted, but are not
immunodominant for both haplotypes. In addition, we show that the
CD4+ T cells induced are of the Th1 phenotype that produce
IFN-
at levels similar to CD4+ T cells induced to
endogenous listerial Ags. These studies suggest that chromosomally
modified strains of L. monocytogenes may be useful as
vaccine vectors for the induction of Th1 T cell responses against
HIV.
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