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Va14Ja18 natural T (iNKT) cells are innate, immunoregulatory lymphocytes that recognize CD1d-restricted lipid Ags such as alpha-galactosylceramide (alpha GalCer). The immunoregulatory functions of iNKT cells are dependent upon either IFN-gamma or IL-4 production by these cells. We hypothesized that alpha GalCer presentation by different CD1d-positive cell types elicits distinct iNKT cell functions. In this study we report that dendritic cells (DC) play a critical role in alpha GalCer-mediated activation of iNKT cells and subsequent transactivation of NK cells. Remarkably, B lymphocytes suppress DC-mediated iNKT and NK cell activation. Nevertheless, alpha GalCer presentation by B cells elicits low IL-4 responses from iNKT cells. This finding is particularly interesting because we demonstrate that NOD DC are defective in eliciting iNKT cell function, but their B cells preferentially activate this T cell subset to secrete low levels of IL-4. Thus, the differential immune outcome based on the type of APC that displays glycolipid Ags in vivo has implications for the design of therapies that harness the immunoregulatory functions of iNKT cells.

Original publication

DOI

10.4049/jimmunol.174.8.4696

Type

Journal article

Journal

Journal of immunology (Baltimore, Md. : 1950)

Publication Date

04/2005

Volume

174

Pages

4696 - 4705

Addresses

Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

Keywords

B-Lymphocytes, Dendritic Cells, Killer Cells, Natural, T-Lymphocyte Subsets, Macrophages, Animals, Mice, Inbred C57BL, Mice, Inbred NOD, Mice, Transgenic, Humans, Mice, Galactosylceramides, Intercellular Signaling Peptides and Proteins, Receptors, Cell Surface, Interleukin-4, Antigens, Lymphocyte Activation, Cell Communication, Immunity, Innate, Interferon-gamma