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CD4+CD25+ regulatory T cells control CD8+ T-cell effector differentiation by modulating IL-2 homeostasis
被引:143
作者:
McNally, Alice
[1
]
Hill, Geoffrey R.
[2
]
Sparwasser, Tim
[3
]
Thomas, Ranjeny
[1
]
Steptoe, Raymond J.
[1
]
机构:
[1] Univ Queensland, Diamantina Inst, Brisbane, Qld 4072, Australia
[2] Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[3] Zentrum Expt & Klin Infekt Forsch, Inst Infekt Immunol, D-30625 Hannover, Germany
来源:
基金:
英国医学研究理事会;
澳大利亚研究理事会;
澳大利亚国家健康与医学研究理事会;
关键词:
HERPES-SIMPLEX-VIRUS;
INTERLEUKIN-2;
PRODUCTION;
AUTOIMMUNE-DISEASE;
DENDRITIC CELLS;
REG CELLS;
RESPONSES;
MICE;
INDUCTION;
TOLERANCE;
RECEPTOR;
D O I:
10.1073/pnas.1103782108
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:
CD4(+)CD25(+) regulatory T cells (Treg) play a crucial role in the regulation of immune responses. Although many mechanisms of Treg suppression in vitro have been described, the mechanisms by which Treg modulate CD8(+) T cell differentiation and effector function in vivo are more poorly defined. It has been proposed, in many instances, that modulation of cytokine homeostasis could be an important mechanism by which Treg regulate adaptive immunity; however, direct experimental evidence is sparse. Here we demonstrate that CD4(+)CD25(+) Treg, by critically regulating IL-2 homeostasis, modulate CD8(+) T-cell effector differentiation. Expansion and effector differentiation of CD8(+) T cells is promoted by autocrine IL-2 but, by competing for IL-2, Treg limit CD8(+) effector differentiation. Furthermore, a regulatory loop exists between Treg and CD8(+) effector T cells, where IL-2 produced during CD8(+) T-cell effector differentiation promotes Treg expansion.
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页码:7529 / 7534
页数:6
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