A Pivotal Role for CD40-Mediated IL-6 Production by Dendritic Cells during IL-17 Induction In Vivo
Author(s) -
Georgia PeronaWright,
Stephen J. Jenkins,
Richard A. O’Connor,
Dimitrios Tomasz Zienkiewicz,
Henry J. McSorley,
Rick M. Maizels,
Stephen M. Anderton,
Andrew S. MacDonald
Publication year - 2009
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.0803553
Subject(s) - cd40 , priming (agriculture) , in vivo , propionibacterium acnes , immunology , cytokine , experimental autoimmune encephalomyelitis , in vitro , biology , dendritic cell , microbiology and biotechnology , immune system , bacteria , cytotoxic t cell , biochemistry , botany , germination , genetics
The costimulatory requirements for Th17 development remain to be defined. In this study, we show that CD40-deficient animals immunized with the gram-positive bacterium Propionibacterium acnes were specifically impaired in their ability to mount an IL-17 response, but not that of IFN-gamma. The same cytokine imbalance resulted from in vivo priming with pathogen-pulsed, CD40-deficient dendritic cells (DC). Engagement of CD40 on P. acnes-conditioned DC stimulated the release of IL-12, IL-23, and IL-6, of which IL-6 alone proved essential for Th17 differentiation. Compared with wild-type DC, priming with those lacking expression of CD40 resulted in reduced disease severity during experimental autoimmune encephalomyelitis, coincident with reduced IL-17 production. Our data delineate sequential requirements for DC expression of CD40 and production of IL-6 during Th17 polarization in vitro and in vivo, and reveal distinct costimulatory requirements for Th1 vs Th17 generation.
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