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Francis R. Carbone

Researcher at University of Melbourne

Publications -  216
Citations -  37352

Francis R. Carbone is an academic researcher from University of Melbourne. The author has contributed to research in topics: Cytotoxic T cell & T cell. The author has an hindex of 83, co-authored 213 publications receiving 35098 citations. Previous affiliations of Francis R. Carbone include Cooperative Research Centre & Washington University in St. Louis.

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The CD8α+ Dendritic Cell Is Responsible for Inducing Peripheral Self-Tolerance to Tissue-associated Antigens

TL;DR: It is indicated that CD8α+ DCs play a critical role in both tolerance and immunity to cell-associated antigens, providing a potential mechanism by which cytotoxic T lymphocyte can be immunized to viral antigen while maintaining tolerance to self.
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Dendritic cell-induced memory T cell activation in nonlymphoid tissues.

TL;DR: Results revealed that memory CD8+ T cell responses can be initiated within peripheral tissues through a tripartite interaction that includes CD4+ T cells and recruited dendritic cells, lending evidence for the existence of a sophisticated T cell response mechanism in extra-lymphoid tissues that can act to control localized infection.
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The dominant role of CD8+ dendritic cells in cross-presentation is not dictated by antigen capture

TL;DR: Mouse spleens contain three populations of conventional (CD11c(high)) dendritic cells (DCs) that play distinct functions, and results indicate that cross-presentation requires specialized machinery that is expressed by CD8(+) DC but largely absent fromCD8(-) DC.
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Cognate CD4+ T cell licensing of dendritic cells in CD8+ T cell immunity

TL;DR: It is shown here that help is essential for the generation of CTL immunity to herpes simplex virus 1 and that CD4+ T cells mediate help in a cognate, antigen-specific way and that C TL immunity may be heavily dependent on cognate DC licensing.
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Dendritic cell subsets in primary and secondary T cell responses at body surfaces

TL;DR: This work examines the role of dendritic cells subsets in immunity to peripheral infections, with emphasis on the differences in the regulation of primary and secondary T cell responses to viruses.