Affiliation:
1. Center for Vaccine Development, Department of Pediatrics
2. Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201
Abstract
ABSTRACT
We investigated the ability of live attenuated
Salmonella enterica
serovar Typhi strains delivered to mice intranasally to induce specific cytotoxic T-lymphocyte (CTL) responses at regional and systemic levels. Mice immunized with two doses (28 days apart) of
Salmonella
serovar Typhi strain Ty21a, the licensed oral typhoid vaccine, and genetically attenuated mutants CVD 908 (Δ
aroC
Δ
aroD
), CVD 915 (Δ
guaBA
), and CVD 908-
htrA
(Δ
aroC
Δ
aroD
Δ
htrA
) induced CTL specific for
Salmonella
serovar Typhi-infected cells in spleens and cervical lymph nodes. CTL were detected in effector T cells that had been expanded in vitro for 7 days in the presence of
Salmonella
-infected syngeneic splenocytes. A second round of stimulation further enhanced the levels of specific cytotoxicity. CTL activity was observed in sorted αβ
+
CD8
+
T cells, which were remarkably increased after expansion, but not in CD4
+
T cells. CTL from both cervical lymph nodes and spleens failed to recognize
Salmonella
-infected major histocompatibility complex (MHC)-mismatched cells, indicating that the responses were MHC restricted. Studies in which MHC blocking antibodies were used showed that H-2L
d
was the restriction element. This is the first demonstration that
Salmonella
serovar Typhi vaccines delivered intranasally elicit CD8
+
MHC class I-restricted CTL. The results further support the usefulness of the murine intranasal model for evaluating the immunogenicity of typhoid vaccine candidates at the preclinical level.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
24 articles.
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