Natural killer activating receptors trigger interferon γ secretion from T cells and natural killer cells

被引:58
作者
Mandelboim, O
Kent, S
Davis, DM
Wilson, SB
Okazaki, T
Jackson, R
Hafler, D
Strominger, JL
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 01238 USA
[2] Joslin Diabet Ctr, Immunol Sect, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.95.7.3798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proliferation of human CD4+ alpha beta T cells expressing a natural killer cell activating receptor (NKAR) has been shown to be enhanced, particularly in response to low doses of antigen, if the target cells present appropriate human class I major histocompatibility complex (MHC) molecules. Here, we show that NKAR also enhance proliferation and killing of target cells by subsets of CD8+ alpha beta and CD8+ gamma delta T cells, as well as by NK cells. Strikingly, interferon gamma secretion from all of these types of lymphocytes was markedly increased by interaction of the NKAR with their MHC class I ligands, independently of enhancement of proliferation. Thus, the recognition of class I MHC molecules by NKAR on both T cells and NK cells may provide a regulatory mechanism that affects immune responses through the secretion of interferon gamma and possibly other cytokines. It represents a signal for cytokine secretion alternative and/or augmentative to that through the T cell receptor.
引用
收藏
页码:3798 / 3803
页数:6
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