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Cutting Edge: Dendritic Cell-Restricted Antigen Presentation Initiates the Follicular Helper T Cell Program but Cannot Complete Ultimate Effector Differentiation
Author(s) -
Radhika Goenka,
Lisa G. Barnett,
Jonathan S. Silver,
Patrick J. O’Neill,
Christopher A. Hunter,
Michael P. Cancro,
Terri M. Laufer
Publication year - 2011
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.1100853
Subject(s) - germinal center , antigen presenting cell , microbiology and biotechnology , cd40 , priming (agriculture) , t cell , effector , antigen presentation , cytotoxic t cell , bcl6 , biology , follicular dendritic cells , dendritic cell , mhc class ii , interleukin 21 , immunology , b cell , antigen , immune system , in vitro , antibody , genetics , germination , botany
Follicular helper T (T(FH)) cells are critical for germinal center (GC) formation. The processes that drive their generation and effector potential remain unclear. In this study, we define requirements for MHC class II APCs in murine T(FH) cell formation by either transiently ablating or restricting Ag presentation to dendritic cells (DCs). We find that cognate interactions with DCs are necessary and sufficient to prime CD4(+) T cells toward a CXCR5(+)ICOS(+)Bcl6(+) T(FH) cell intermediate. However, in the absence of additional APCs, these T(FH) cells fail to produce IL-21. Furthermore, in vitro priming of naive T cells by B cells engenders optimal production of IL-21, which induces a GC B cell transcriptional profile. These results support a multistep model for effector T(FH) cell priming and GC initiation, in which DCs are necessary and sufficient to induce a T(FH) cell intermediate that requires additional interactions with distinct APCs for full effector function.

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