Innate immunity defines the capacity of antiviral T cells to limit persistent infection

被引:175
作者
Andrews, Daniel M. [1 ,3 ]
Estcourt, Marie J. [1 ,3 ]
Andoniou, Christopher E. [1 ,3 ]
Wikstrom, Matthew E. [1 ,3 ]
Khong, Andrea [1 ,3 ]
Voigt, Valentina [1 ,3 ]
Fleming, Peter [1 ,3 ]
Tabarias, Hyacinth [1 ,3 ]
Hill, Geoffrey R. [4 ]
van der Most, Robbert G. [2 ]
Scalzo, Anthony A. [1 ,3 ]
Smyth, Mark J. [5 ]
Degli-Esposti, Mariapia A. [1 ,3 ]
机构
[1] Univ Western Australia, Ctr Ophthalmol & Visual Sci, Immunol & Virol Program, Nedlands, WA 6009, Australia
[2] Univ Western Australia, Univ Dept Med, Nedlands, WA 6009, Australia
[3] Lions Eye Inst, Ctr Expt Immunol, Nedlands, WA 6009, Australia
[4] Queensland Inst Med Res, Bone Marrow Transplantat Lab, Herston, Qld 4006, Australia
[5] Peter MacCallum Canc Ctr, Sir Donald & Lady Trescowthick Labs, Canc Immunol Program, Melbourne, Vic 3002, Australia
基金
英国惠康基金; 英国医学研究理事会;
关键词
MURINE CYTOMEGALOVIRUS-INFECTION; NATURAL-KILLER-CELLS; DENDRITIC CELLS; MOUSE CYTOMEGALOVIRUS; NK CELLS; RESPONSES; ACTIVATION; GENE; RECOGNITION; PROTECTION;
D O I
10.1084/jem.20091193
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Effective immunity requires the coordinated activation of innate and adaptive immune responses. Natural killer (NK) cells are central innate immune effectors, but can also affect the generation of acquired immune responses to viruses and malignancies. How NK cells influence the efficacy of adaptive immunity, however, is poorly understood. Here, we show that NK cells negatively regulate the duration and effectiveness of virus-specific CD4(+) and CD8(+) T cell responses by limiting exposure of T cells to infected antigen-presenting cells. This impacts the quality of T cell responses and the ability to limit viral persistence. Our studies provide unexpected insights into novel interplays between innate and adaptive immune effectors, and define the critical requirements for efficient control of viral persistence.
引用
收藏
页码:1333 / 1343
页数:11
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