| Literature DB >> 15356117 |
Alessandra Zingoni1, Thierry Sornasse, Benjamin G Cocks, Yuetsu Tanaka, Angela Santoni, Lewis L Lanier.
Abstract
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. Copyright 2004 The American Association of Immunologists, Inc.Entities:
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Year: 2004 PMID: 15356117 DOI: 10.4049/jimmunol.173.6.3716
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422