Autocrine IFN-γ Promotes Naive CD8 T Cell Differentiation and Synergizes with IFN-α To Stimulate Strong Function

被引:75
作者
Curtsinger, Julie M. [1 ]
Agarwal, Pujya [1 ]
Lins, Debra C. [1 ]
Mescher, Matthew F. [1 ]
机构
[1] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
INTERFERON-GAMMA; CLONAL EXPANSION; MEMORY DEVELOPMENT; EFFECTOR FUNCTION; DENDRITIC CELLS; CUTTING EDGE; ANTIGEN; IL-12; BET; RECEPTOR;
D O I
10.4049/jimmunol.1102727
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autocrine IFN-gamma signaling is important for CD4 differentiation to Th1 effector cells, but it has been unclear whether it contributes to CD8 T cell differentiation. We show in this paper that naive murine CD8 T cells rapidly and transiently produce low levels of IFN-gamma upon stimulation with Ag and B7-1, with production peaking at similar to 8 h and declining by 24 h. The autocrine IFN-gamma signals for upregulation of expression of T-bet and granzyme B and induces weak cytolytic activity and effector IFN-gamma production. IFN-alpha acts synergistically with IFN-gamma to support development of strong effector functions, whereas IL-12 induces high T-bet expression and strong function in the absence of IFN-gamma signaling. Thus, IFN-gamma is not only an important CD8 T cell effector cytokine, it is an autocrine/paracrine factor whose contributions to differentiation vary depending on whether the response is supported by IL-12 or type I IFN. The Journal of Immunology, 2012, 189: 659-668.
引用
收藏
页码:659 / 668
页数:10
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