T-bet regulates differentiation of forkhead box protein 3+ regulatory T cells in programmed cell death-1-deficient mice

被引:5
|
作者
Tahara, M. [1 ]
Kondo, Y. [1 ]
Yokosawa, M. [1 ]
Tsuboi, H. [1 ]
Takahashi, S. [2 ,3 ]
Shibayama, S. [4 ]
Matsumoto, I. [1 ]
Sumida, T. [1 ]
机构
[1] Univ Tsukuba, Fac Med, Dept Internal Med, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Dept Anat & Embryol, Fac Med, Tsukuba, Ibaraki 3058575, Japan
[3] Univ Tsukuba, Lab Anim Resource Ctr, Tsukuba, Ibaraki 3058575, Japan
[4] Tsukuba Inst ONO Pharmaceut Co LTD, Tsukuba, Ibaraki, Japan
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2015年 / 179卷 / 02期
关键词
FoxP3(+) regulatory T cells; helper T cell subsets; programmed cell death-1; T cell tolerance; Th1; cells; SYSTEMIC-LUPUS-ERYTHEMATOSUS; TRANSCRIPTION FACTOR; CONTACT-DERMATITIS; EXPERIMENTAL COLITIS; INHIBITORY RECEPTOR; MURINE MODEL; SCURFY MICE; PD-1; MOUSE; EXPRESSION;
D O I
10.1111/cei.12455
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Programmed cell death-1 (PD-1) plays an important role in peripheral T cell tolerance, but whether or not it affects the differentiation of helper T cell subsets remains elusive. Here we describe the importance of PD-1 in the control of T helper type 1 (Th1) cell activation and development of forkhead box protein 3 (FoxP3(+)) regulatory T cells (T-regs). PD-1-deficient T cell-specific T-bet transgenic (P/T) mice showed growth retardation, and the majority died within 10 weeks. P/T mice showed T-bet over-expression, increased interferon (IFN)- production by CD4(+) T cells and significantly low FoxP3(+) T-reg cell percentage. P/T mice developed systemic inflammation, which was probably induced by augmented Th1 response and low FoxP3(+) T-reg count. The study identified a unique, previously undescribed role for PD-1 in Th1 and T-reg differentiation, with potential implication in the development of Th1 cell-targeted therapy.
引用
收藏
页码:197 / 209
页数:13
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