Primed Antigen-Specific CD4+ T Cells Are Required for NK Cell Activation In Vivo upon Leishmania major Infection
Author(s) -
Franck Bihl,
Julien Pecheur,
Béatrice Breart,
Gwénola Poupon,
Julie Cazareth,
Valérie Julia,
Nicolas Glaichenhaus,
Véronique M. Braud
Publication year - 2010
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1001486
Subject(s) - interleukin 12 , cd40 , microbiology and biotechnology , secretion , interleukin 21 , biology , antigen presenting cell , acquired immune system , innate immune system , immunology , t cell , antigen , cytotoxic t cell , immune system , in vitro , biochemistry
The ability of NK cells to rapidly produce IFN-gamma is an important innate mechanism of resistance to many pathogens including Leishmania major. Molecular and cellular components involved in NK cell activation in vivo are still poorly defined, although a central role for dendritic cells has been described. In this study, we demonstrate that Ag-specific CD4(+) T cells are required to initiate NK cell activation early on in draining lymph nodes of L. major-infected mice. We show that early IFN-gamma secretion by NK cells is controlled by IL-2 and IL-12 and is dependent on CD40/CD40L interaction. These findings suggest that newly primed Ag-specific CD4(+) T cells could directly activate NK cells through the secretion of IL-2 but also indirectly through the regulation of IL-12 secretion by dendritic cells. Our results reveal an unappreciated role for Ag-specific CD4(+) T cells in the initiation of NK cell activation in vivo upon L. major infection and demonstrate bidirectional regulations between innate and adaptive immunity.
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