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Regulation of innate CD8+ T-cell activation mediated by cytokines
被引:187
|作者:
Freeman, Bailey E.
[1
]
Hammarlund, Erika
[1
]
Raue, Hans-Peter
[1
]
Slifka, Mark K.
[1
]
机构:
[1] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Beaverton, OR 97006 USA
来源:
基金:
美国国家卫生研究院;
关键词:
lymphocytic choriomeningitis virus;
mouse;
interleukin;
lymphocyte;
GAMMA-INDUCING FACTOR;
IFN-GAMMA;
INTERFERON-ALPHA/BETA;
BYSTANDER ACTIVATION;
GENE-EXPRESSION;
IL-12;
INHIBITION;
MECHANISM;
RESPONSES;
PROMOTION;
D O I:
10.1073/pnas.1203543109
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:
Virus-specific CD8(+) T cells develop the ability to function in an "innate" capacity by responding to a remarkable array of cytokines in a TCR-independent manner. Although several cytokines such as IL-12 and IL-18 have been identified as key regulators of CD8(+) T-cell activation, the role of other cytokines and the ways in which they interact with each other remain unclear. Here, we have used an unbiased, systematic approach to examine the effects of 1,849 cytokine combinations on virus-specific CD8(+) T-cell activation. This study identifies several unexpected cytokine combinations that synergize to induce antigen-independent IFN gamma production and CD69 up-regulation by CD8(+) T cells in addition to cytokines that exhibit differential regulatory functions, with the ability to either enhance or inhibit T-cell IFN gamma production, depending on which cytokine partner is present. These findings underscore the complexity of cytokine interactions while also providing insight into the multifaceted regulatory network controlling virus-specific CD8(+) T-cell functions.
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页码:9971 / 9976
页数:6
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