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T-bet调节程序性细胞死亡蛋白1缺陷小鼠中叉头框蛋白3+调节性T细胞的分化。

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

作者信息

Tahara M, Kondo Y, Yokosawa M, Tsuboi H, Takahashi S, Shibayama S, Matsumoto I, Sumida T

机构信息

Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.

出版信息

Clin Exp Immunol. 2015 Feb;179(2):197-209. doi: 10.1111/cei.12455.

Abstract

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 (Tr(egs)). 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)-γ 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.

摘要

程序性细胞死亡蛋白1(PD-1)在外周T细胞耐受中起重要作用,但它是否影响辅助性T细胞亚群的分化仍不清楚。在此,我们描述了PD-1在控制1型辅助性T细胞(Th1)激活和叉头框蛋白3(FoxP3(+))调节性T细胞(Tr(egs))发育中的重要性。PD-1缺陷的T细胞特异性T-bet转基因(P/T)小鼠出现生长发育迟缓,大多数在10周内死亡。P/T小鼠表现出T-bet过度表达,CD4(+) T细胞产生的干扰素(IFN)-γ增加,且FoxP3(+) T(reg)细胞百分比显著降低。P/T小鼠发生全身性炎症,这可能是由增强的Th1反应和低FoxP3(+) T(reg)细胞计数诱导的。该研究确定了PD-1在Th1和T(reg)分化中一个独特的、以前未描述的作用,这对Th1细胞靶向治疗的发展具有潜在意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5df3/4298397/938efdb02c14/cei0179-0197-f1.jpg

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