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Directed antigen delivery as a vaccine strategy for an intracellular bacterial pathogen.


ABSTRACT: We have developed a vaccine strategy for generating an attenuated strain of an intracellular bacterial pathogen that, after uptake by professional antigen-presenting cells, does not replicate intracellularly and is readily killed. However, after degradation of the vaccine strain within the phagolysosome, target antigens are released into the cytosol for endogenous processing and presentation for stimulation of CD8(+) effector T cells. Applying this strategy to the model intracellular pathogen Listeria monocytogenes, we show that an intracellular replication-deficient vaccine strain is cleared rapidly in normal and immunocompromised animals, yet antigen-specific CD8(+) effector T cells are stimulated after immunization. Furthermore, animals immunized with the intracellular replication-deficient vaccine strain are resistant to lethal challenge with a virulent WT strain of L. monocytogenes. These studies suggest a general strategy for developing safe and effective, attenuated intracellular replication-deficient vaccine strains for stimulation of protective immune responses against intracellular bacterial pathogens.

SUBMITTER: Bouwer HG 

PROVIDER: S-EPMC1458801 | biostudies-other | 2006 Mar

REPOSITORIES: biostudies-other

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Directed antigen delivery as a vaccine strategy for an intracellular bacterial pathogen.

Bouwer H G Archie HG   Alberti-Segui Christine C   Montfort Megan J MJ   Berkowitz Nathan D ND   Higgins Darren E DE  

Proceedings of the National Academy of Sciences of the United States of America 20060320 13


We have developed a vaccine strategy for generating an attenuated strain of an intracellular bacterial pathogen that, after uptake by professional antigen-presenting cells, does not replicate intracellularly and is readily killed. However, after degradation of the vaccine strain within the phagolysosome, target antigens are released into the cytosol for endogenous processing and presentation for stimulation of CD8(+) effector T cells. Applying this strategy to the model intracellular pathogen Li  ...[more]

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