Regulatory T Cells Increase the Avidity of Primary CD8+ T Cell Responses and Promote Memory

被引:124
|
作者
Pace, Luigia [1 ]
Tempez, Andy [1 ]
Arnold-Schrauf, Catharina [2 ]
Lemaitre, Fabrice [3 ]
Bousso, Philippe [3 ]
Fetler, Luc [4 ]
Sparwasser, Tim [2 ]
Amigorena, Sebastian [1 ]
机构
[1] Inst Curie, INSERM, U932, F-75248 Paris 05, France
[2] TWINCORE, Ctr Expt & Clin Infect Res, Inst Infect Immunol, D-30625 Hannover, Germany
[3] Inst Pasteur, INSERM, U668, Dept Immunol, F-75015 Paris, France
[4] Inst Curie, CNRS, UMR 168, Lab Physicochim Curie, F-75248 Paris 05, France
关键词
DENDRITIC CELLS; IN-VIVO; PEPTIDE; REPERTOIRE; ANTIGEN; MHC; SELECTION; IMMUNITY; AUTOIMMUNITY; TOLERANCE;
D O I
10.1126/science.1227049
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
Although regulatory T cells (T-regs) are known to suppress self-reactive autoimmune responses, their role during T cell responses to nonself antigens is not well understood. We show that T-regs play a critical role during the priming of immune responses in mice. T-reg depletion induced the activation and expansion of a population of low-avidity CD8(+) T cells because of overproduction of CCL-3/4/5 chemokines, which stabilized the interactions between antigen-presenting dendritic cells and low-avidity T cells. In the absence of T-regs, the avidity of the primary immune response was impaired, which resulted in reduced memory to Listeria monocytogenes. These results suggest that T-regs are important regulators of the homeostasis of CD8(+) T cell priming and play a critical role in the induction of high-avidity primary responses and effective memory.
引用
收藏
页码:532 / 536
页数:5
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