IL-21R on T Cells Is Critical for Sustained Functionality and Control of Chronic Viral Infection

被引:364
作者
Froehlich, Anja [1 ]
Kisielow, Jan [1 ]
Schmitz, Iwana [1 ]
Freigang, Stefan [1 ]
Shamshiev, Abdijapar T. [1 ]
Weber, Jacqueline [1 ]
Marsland, Benjamin J. [1 ]
Oxenius, Annette [2 ]
Kopf, Manfred [1 ]
机构
[1] ETH, Inst Integrat Biol, Zurich, Switzerland
[2] ETH, Inst Microbiol, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
HOMEOSTATIC PROLIFERATION; IN-VIVO; RESPONSES; EFFECTOR; HIV-1;
D O I
10.1126/science.1172815
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
Chronic viral infection is often associated with the dysfunction of virus-specific T cells. Our studies using Il21r-deficient (Il21r(-/-)) mice now suggest that interleukin-21 (IL-21) is critical for the long-term maintenance and functionality of CD8(+) T cells and the control of chronic lymphocytic choriomeningitis virus infection in mice. Cell-autonomous IL-21 receptor (IL-21R)-dependent signaling by CD8(+) T cells was required for sustained cell proliferation and cytokine production during chronic infection. Il21r(-/-) mice showed normal CD8(+) T cell expansion, effector function, memory homeostasis, and recall responses during acute and after resolved infection with several other nonpersistent viruses. These data suggest that IL-21R signaling is required for the maintenance of polyfunctional T cells during chronic viral infections and have implications for understanding the immune response to other persisting antigens, such as tumors.
引用
收藏
页码:1576 / 1580
页数:5
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