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Cross-Talk between Activated Human NK Cells and CD4+ T Cells via OX40-OX40 Ligand Interactions
Author(s) -
Alessandra Zingoni,
Thierry Sornasse,
Benjamin G. Cocks,
Yuetsu Tanaka,
Angela Santoni,
Lewis L. Lanier
Publication year - 2004
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.173.6.3716
Subject(s) - nkg2d , microbiology and biotechnology , cd16 , interleukin 21 , interleukin 12 , zap70 , natural killer t cell , biology , receptor , immune system , t cell , cytotoxic t cell , immunology , cd8 , cd3 , in vitro , biochemistry
It is important to understand which molecules are relevant for linking innate and adaptive immune cells. In this study, we show that OX40 ligand is selectively induced on IL-2, IL-12, or IL-15-activated human NK cells following stimulation through NKG2D, the low affinity receptor for IgG (CD16) or killer cell Ig-like receptor 2DS2. CD16-activated NK cells costimulate TCR-induced proliferation, and IFN-gamma produced by autologous CD4+ T cells and this process is dependent upon expression of OX40 ligand and B7 by the activated NK cells. These findings suggest a novel and unexpected link between the natural and specific immune responses, providing direct evidence for cross-talk between human CD4+ T cells and NK receptor-activated NK cells.

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