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1
Extrathymic generation of regulatory T cells in placental mammals mitigates maternal-fetal conflict.胎盘哺乳动物的胸腺外生成调节性 T 细胞可减轻母婴冲突。
Cell. 2012 Jul 6;150(1):29-38. doi: 10.1016/j.cell.2012.05.031.
2
T-cell tolerance: central and peripheral.T 细胞耐受:中枢与外周。
Cold Spring Harb Perspect Biol. 2012 Jun 1;4(6):a006957. doi: 10.1101/cshperspect.a006957.
3
Loss of epigenetic modification driven by the Foxp3 transcription factor leads to regulatory T cell insufficiency.Foxp3 转录因子驱动的表观遗传修饰缺失导致调节性 T 细胞功能不足。
Immunity. 2012 May 25;36(5):717-30. doi: 10.1016/j.immuni.2012.03.020. Epub 2012 May 10.
4
An N-terminal mutation of the Foxp3 transcription factor alleviates arthritis but exacerbates diabetes.Foxp3 转录因子的 N 端突变可缓解关节炎,但会加重糖尿病。
Immunity. 2012 May 25;36(5):731-41. doi: 10.1016/j.immuni.2012.04.007. Epub 2012 May 10.
5
Nuclear receptor Nr4a1 modulates both regulatory T-cell (Treg) differentiation and clonal deletion.核受体 Nr4a1 调节调节性 T 细胞 (Treg) 分化和克隆删除。
Proc Natl Acad Sci U S A. 2012 Mar 6;109(10):3891-6. doi: 10.1073/pnas.1200090109. Epub 2012 Feb 15.
6
Plasticity of Foxp3(+) T cells reflects promiscuous Foxp3 expression in conventional T cells but not reprogramming of regulatory T cells.Foxp3(+) T 细胞的可塑性反映了常规 T 细胞中 Foxp3 的混杂表达,而不是调节性 T 细胞的重新编程。
Immunity. 2012 Feb 24;36(2):262-75. doi: 10.1016/j.immuni.2011.12.012. Epub 2012 Feb 9.
7
Expression of Helios in peripherally induced Foxp3+ regulatory T cells.外周诱导的 Foxp3+调节性 T 细胞中 Helios 的表达。
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8
Peripheral education of the immune system by colonic commensal microbiota.肠道共生菌群对免疫系统的外周教育。
Nature. 2011 Sep 21;478(7368):250-4. doi: 10.1038/nature10434.
9
Helios expression is a marker of T cell activation and proliferation.Helios 表达是 T 细胞活化和增殖的标志物。
PLoS One. 2011;6(8):e24226. doi: 10.1371/journal.pone.0024226. Epub 2011 Aug 30.
10
CD4⁺CD25⁺Foxp3⁺ regulatory T cell formation requires more specific recognition of a self-peptide than thymocyte deletion.CD4⁺CD25⁺Foxp3⁺调节性 T 细胞的形成需要比胸腺细胞删除更特异性地识别自身肽。
Proc Natl Acad Sci U S A. 2011 Sep 6;108(36):14890-5. doi: 10.1073/pnas.1103810108. Epub 2011 Aug 22.

调节性 T 细胞,其生命周期和多样性。

Treg cells, life history, and diversity.

机构信息

Division of Immunology, Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cold Spring Harb Perspect Biol. 2012 Sep 1;4(9):a007021. doi: 10.1101/cshperspect.a007021.

DOI:10.1101/cshperspect.a007021
PMID:22952391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428763/
Abstract

Regulatory T cells expressing the FoxP3 transcription factor have a profound and nonredundant role in several aspects of immunological tolerance. We will review here the specification of this lineage, its population dynamics, and the diversity of subphenotypes that correlate with their diverse roles in controlling inflammation in a variety of settings.

摘要

表达转录因子 FoxP3 的调节性 T 细胞在免疫耐受的几个方面发挥着深远且不可或缺的作用。我们将在这里回顾该谱系的特异性、其群体动力学以及与其在各种环境中控制炎症的多种作用相关的多种亚表型的多样性。