Cross-talk between activated human NK cells and CD4+ T cells via OX40-OX40 ligand interactions

被引:209
作者
Zingoni, A
Sornasse, T
Cocks, BG
Tanaka, Y
Santoni, A
Lanier, LL
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Canc Res, San Francisco, CA 94143 USA
[3] Univ Roma La Sapienza, Dept Expt Med & Pathol, Rome, Italy
[4] Incyte Corp, Palo Alto, CA 94304 USA
[5] Univ Ryukyus, Grad Sch, Dept Immunol, Okinawa, Japan
[6] Univ Ryukyus, Fac Med, Dept Immunol, Okinawa, Japan
关键词
D O I
10.4049/jimmunol.173.6.3716
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:3716 / 3724
页数:9
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