Listeria-Infected Myeloid Dendritic Cells Produce IFN-β, Priming T Cell Activation
Author(s) -
Hanping Feng,
Dong Zhang,
Deborah Palliser,
Pengcheng Zhu,
Shenghe Cai,
Ann Schlesinger,
Laura Maliszewski,
Judy Lieberman
Publication year - 2005
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.175.1.421
Subject(s) - listeria monocytogenes , priming (agriculture) , t cell , secretion , intracellular , microbiology and biotechnology , listeria , biology , intracellular parasite , dendritic cell , bacteria , immune system , immunology , biochemistry , botany , genetics , germination
The intracellular bacterium Listeria monocytogenes infects dendritic cells (DC) and other APCs and induces potent cell-mediated protective immunity. However, heat-killed bacteria fail to do so. This study explored whether DC differentially respond to live and killed Listeria and how this affects T cell activation. To control for bacterial number, a replication-deficient strain, Lmdd, defective in D-alanine biosynthesis, was used. We found that DC internalize both live and heat-killed Lmdd and similarly up-regulate the expression of costimulatory molecules, a necessary step for T cell activation. However, only live Lmdd-infected DC stimulate T cells to express the early activation marker CD69 and enhance T cell activation upon TCR engagement. Infection with live, but not heat-killed, Lmdd induces myeloid DC to secrete copious amounts of IFN-beta, which requires bacterial cytosolic invasion. Exposure to high concentrations of IFN-beta sensitizes naive T cells for Ag-dependent activation.
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