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T 记忆样 T-PLL 细胞的非典型效应功能是由 TCL1A 和 TCR 信号的协同作用塑造的。

Noncanonical effector functions of the T-memory-like T-PLL cell are shaped by cooperative TCL1A and TCR signaling.

机构信息

Department I of Internal Medicine, Center for Integrated Oncology Aachen-Bonn-Cologne-Duesseldorf.

CECAD Center of Excellence on Cellular Stress Responses in Aging-Associated Diseases, and.

出版信息

Blood. 2020 Dec 10;136(24):2786-2802. doi: 10.1182/blood.2019003348.

Abstract

T-cell prolymphocytic leukemia (T-PLL) is a poor-prognostic neoplasm. Differentiation stage and immune-effector functions of the underlying tumor cell are insufficiently characterized. Constitutive activation of the T-cell leukemia 1A (TCL1A) oncogene distinguishes the (pre)leukemic cell from regular postthymic T cells. We assessed activation-response patterns of the T-PLL lymphocyte and interrogated the modulatory impact by TCL1A. Immunophenotypic and gene expression profiles revealed a unique spectrum of memory-type differentiation of T-PLL with predominant central-memory stages and frequent noncanonical patterns. Virtually all T-PLL expressed a T-cell receptor (TCR) and/or CD28-coreceptor without overrepresentation of specific TCR clonotypes. The highly activated leukemic cells also revealed losses of negative-regulatory TCR coreceptors (eg, CTLA4). TCR stimulation of T-PLL cells evoked higher-than-normal cell-cycle transition and profiles of cytokine release that resembled those of normal memory T cells. More activated phenotypes and higher TCL1A correlated with inferior clinical outcomes. TCL1A was linked to the marked resistance of T-PLL to activation- and FAS-induced cell death. Enforced TCL1A enhanced phospho-activation of TCR kinases, second-messenger generation, and JAK/STAT or NFAT transcriptional responses. This reduced the input thresholds for IL-2 secretion in a sensitizer-like fashion. Mice of TCL1A-initiated protracted T-PLL development resembled such features. When equipped with epitope-defined TCRs or chimeric antigen receptors, these Lckpr-hTCL1Atg T cells gained a leukemogenic growth advantage in scenarios of receptor stimulation. Overall, we propose a model of T-PLL pathogenesis in which TCL1A enhances TCR signals and drives the accumulation of death-resistant memory-type cells that use amplified low-level stimulatory input, and whose loss of negative coregulators additionally maintains their activated state. Treatment rationales are provided by combined interception in TCR and survival signaling.

摘要

T 细胞前淋巴细胞白血病(T-PLL)是一种预后不良的肿瘤。其肿瘤细胞的分化阶段和免疫效应功能尚未充分阐明。T 细胞白血病 1A(TCL1A)癌基因的组成性激活将前白血病细胞与常规胸腺后 T 细胞区分开来。我们评估了 T-PLL 淋巴细胞的激活反应模式,并研究了 TCL1A 的调节作用。免疫表型和基因表达谱显示了 T-PLL 独特的记忆样分化谱,主要为中央记忆阶段,且经常出现非典型模式。几乎所有 T-PLL 均表达 T 细胞受体(TCR)和/或 CD28 共受体,而无特定 TCR 克隆型的过度表达。高度激活的白血病细胞也显示出负调节 TCR 共受体(例如 CTLA4)的缺失。TCR 刺激 T-PLL 细胞可引发高于正常的细胞周期过渡和细胞因子释放谱,类似于正常记忆 T 细胞的谱。更活跃的表型和更高的 TCL1A 与较差的临床结局相关。TCL1A 与 T-PLL 对激活和 Fas 诱导的细胞死亡的显著抵抗有关。强制表达 TCL1A 增强了 TCR 激酶的磷酸化激活、第二信使的产生以及 JAK/STAT 或 NFAT 转录反应。以敏化剂样方式降低了 IL-2 分泌的输入阈值。TCL1A 引发的持续性 T-PLL 发展的小鼠表现出类似的特征。当配备有表位定义的 TCR 或嵌合抗原受体时,这些 Lckpr-hTCL1Atg T 细胞在受体刺激的情况下获得了白血病生长优势。总的来说,我们提出了 T-PLL 发病机制的模型,其中 TCL1A 增强了 TCR 信号,并驱动了死亡抵抗性记忆样细胞的积累,这些细胞利用放大的低水平刺激输入,并通过丧失负性共调节剂进一步维持其激活状态。通过阻断 TCR 和存活信号的联合干预提供了治疗依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbc5/7731789/fe713832a195/bloodBLD2019003348absf1.jpg

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