Generation of Th1-Polarizing Dendritic Cells Using the TLR7/8 Agonist CL075
Author(s) -
Stefani Spranger,
Miran Javorovic,
Maja Bürdek,
Susanne Wilde,
Barbara Mosetter,
Stefanie Tippmer,
Iris Bigalke,
Christiane Geiger,
Dolores J. Schendel,
Bernhard Frankenberger
Publication year - 2010
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1000060
Subject(s) - microbiology and biotechnology , secretion , agonist , tlr7 , chemotaxis , chemistry , cd8 , t cell , dendritic cell , cytotoxic t cell , cytokine , monocyte , biology , receptor , immunology , immune system , in vitro , biochemistry , toll like receptor , innate immune system
In this paper, we describe a new method for preparation of human dendritic cells (DCs) that secrete bioactive IL-12(p70) using synthetic immunostimulatory compounds as TLR7/8 agonists. Monocyte-derived DCs were generated using a procedure that provided mature cells within 3 d. Several maturation mixtures that contained various cytokines, IFN-gamma, different TLR agonists, and PGE(2) were compared for impact on cell recovery, phenotype, cytokine secretion, migration, and lymphocyte activation. Mixtures that included the TLR7/8 agonists R848 or CL075, combined with the TLR3 agonist polyinosinic:polycytidylic acid, yielded 3-d mature DCs that secreted high levels of IL-12(p70), showed strong chemotaxis to CCR7 ligands, and had a positive costimulatory potential. They also had excellent capacity to activate NK cells, effectively polarized CD4(+) and CD8(+) T cells to secrete IFN-gamma and to induce T cell-mediated cytotoxic function. Thereby, mature DCs prepared within 3 d using such maturation mixtures displayed optimal functions required for vaccine development.
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