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Cross-Presentation of Listeria-Derived CD8 T Cell Epitopes Requires Unstable Bacterial Translation Products
Author(s) -
J. Michael Janda,
Petra Schöneberger,
Mojca Škoberne,
Martin Messerle,
Holger Rüssmann,
Gernot Geginat
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.173.9.5644
Subject(s) - epitope , cross presentation , listeria monocytogenes , cytotoxic t cell , cd8 , antigen presentation , t cell , biology , translation (biology) , bacteria , microbiology and biotechnology , antigen , immune system , chemistry , immunology , messenger rna , biochemistry , genetics , gene , in vitro
Presentation of bacteria-derived CD8 T cell epitopes by dendritic cells (DC) requires either their direct infection or that DC acquire and cross-present Ags from other infected cells. We found that cross-presentation of Listeria monocytogenes-derived CD8 T cell epitopes was much stronger than direct Ag presentation by infected murine DC. Cross-presentation of Listeria-derived CD8 T cell epitopes showed unique physiological requirements. It was dependent upon the delivery of unstable bacterial translation products by infected, but still viable, Ag donor cells. Cross-presentation was enhanced both when unstable translation products in infected Ag donor cells were protected from proteasomal degradation and when the production of misfolded bacterial proteins was increased. The requirement of unstable translation products for cross-presentation may represent a novel pathway that functions to focus the CD8 T cell response toward epitopes derived from newly synthesized proteins.

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