An official website of the United States government.

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Novel role of DC1 in vaccine induced CD8 T cell responses


Project SummaryThe development of vaccines that can specifically generate cell mediated immunity has remained a majorchallenge in the field of vaccinology for both microbial pathogens and cancer. Prior work has shown thatthe use of replication deficient live microbes is one way to generate a potent pathogen-specific CD8+ T cellresponse. For example, even a single low dose of the non-replicating vaccine CPS strain of Toxoplasmagondii elicits a robust parasite specific CD8+ T cell response that provides long-lived protective immunity.However, many questions remain about how the immune system recognizes and processes the antigensfrom these attenuated organisms to prime and expand parasite-specific T cells. Prior work has shown thatthe CD8+ T cell response is dependent on the Batf3-dependent dendritic cells (DC1), which are commonlyinvolved in antigen cross-presentation to CD8+ T cells as well as IL-12 production. Paradoxically,preliminary data indicates that DC1 are not required for early CD8+ T cell priming, but are required togenerate a protective CD8+ T cell response. Importantly, the loss of the autophagy pathway in DC alsoresults in a failure to generate protective CD8+ T cells. These studies emphasize two important questions:1) what priming-independent role do DC1 play in generating a CD8+ T cell response, 2) what autophagy-dependent pathway in DC1 is required for the expansion and differentiation of CD8+ T cells? Theautophagy pathway has been implicated as being required for leukocyte survival in inflammatory setting aswell as an alternative pathway for the processing and presentation of parasite antigen. The studiesproposed here will use a variety of unique microbial tools (fluorescent reporters, parasite auxotrophs, Cre-exressing parasites) and mouse strains (Batf3-/-, unique reporters, and mice which do not express MHCI H-2Kb on DC1) combined with our imaging expertise to address I. Do DC1 interact directly with parasite-specific CD8+ T cells in a peptide-MHCI dependent fashion to provide the signals required for T cellexpansion and differentiation and II. What autophagy-dependent processes in DC1 are required for thegeneration of protective effector CD8+ T cells.

Hunter, Christopher
University of Pennsylvania
Start date
End date
Project number
Accession number