A key control point in the T cell response to chronic infection and neoplasia: FOXO1.

A key control point in the T cell response to chronic infection and neoplasia: FOXO1.
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DOI:
10.1016/j.coi.2020.02.001
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发表时间:
2020-04
影响因子:
7
通讯作者:
Hedrick SM
Hedrick SM
中科院分区:
医学2区
文献类型:
--
作者:
Marcel N;Hedrick SM

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能够控制肿瘤形成或慢性感染的T细胞显示出与中央记忆T细胞相似或相同的特征基因表达谱。这些细胞具有自我更新的性质和可塑性,使它们能够反复经历激活(生长,增殖和分化),然后静止。正是这些品质定义了T细胞与慢性感染因子建立平衡的能力,并且还保留了T细胞响应于恶性癌症而被重新激活(通过检查点疗法)的能力。在这里,我们描述了肿瘤和持久性病毒介导的抑制形式之间的区别,我们回顾了与长期免疫相关的T细胞的特性,我们确定了转录因子FOXO 1作为基因表达程序的控制点,该程序允许CD8+ T细胞进行连续的再激活和自我更新。
T cells able to control neoplasia or chronic infections display a signature gene expression profile similar or identical to that of central memory T cells. These cells have qualities of self-renewal and a plasticity that allow them to repeatedly undergo activation (growth, proliferation, and differentiation), followed by quiescence. It is these qualities that define the ability of T cells to establish an equilibrium with chronic infectious agents, and also preserve the ability of T cells to be re-activated (by checkpoint therapy) in response to malignant cancers. Here we describe distinctions between the forms of inhibition mediated by tumors and persistent viruses, we review the properties of T cells associated with long-term immunity, and we identify the transcription factor, FOXO1, as the control point for a program of gene expression that allows CD8+ T cells to undergo serial reactivation and self-renewal.
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