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Eur J Immunol ; 44(1): 195-203, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24019201

ABSTRACT

CD161(++) CD8(+) T cells represent a novel subset that is dominated in adult peripheral blood by mucosal-associated invariant T (MAIT) cells, as defined by the expression of a variable-α chain 7.2 (Vα7.2)-Jα33 TCR, and IL-18Rα. Stimulation with IL-18+IL-12 is known to induce IFN-γ by both NK cells and, to a more limited extent, T cells. Here, we show the CD161(++) CD8(+) T-cell population is the primary T-cell population triggered by this mechanism. Both CD161(++) Vα7.2(+) and CD161(++) Vα7.2(-) T-cell subsets responded to IL-12+IL-18 stimulation, demonstrating this response was not restricted to the MAIT cells, but to the CD161(++) phenotype. Bacteria and TLR agonists also indirectly triggered IFN-γ expression via IL-12 and IL-18. These data show that CD161(++) T cells are the predominant T-cell population that responds directly to IL-12+IL-18 stimulation. Furthermore, our findings broaden the potential role of MAIT cells beyond bacterial responsiveness to potentially include viral infections and other inflammatory stimuli.


Subject(s)
Interleukin-12/immunology , Interleukin-18/immunology , Mucous Membrane/immunology , Natural Killer T-Cells/immunology , Receptors, Interleukin-18/metabolism , T-Lymphocyte Subsets/immunology , CD8 Antigens/metabolism , Cell Line , Cell Separation , Flow Cytometry , Humans , Interferon-gamma/metabolism , Interleukin-12/pharmacology , Interleukin-18/pharmacology , Lymphocyte Activation , NK Cell Lectin-Like Receptor Subfamily B/metabolism , Receptors, Antigen, T-Cell, alpha-beta/metabolism , T-Lymphocyte Subsets/drug effects
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