TCF-1-Centered Transcriptional Network Drives an Effector versus Exhausted CD8 T Cell-Fate Decision

以TCF-1为中心的转录网络驱动效应CD8 T细胞与耗竭CD8 T细胞的命运决定

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作者:Zeyu Chen ,Zhicheng Ji ,Shin Foong Ngiow ,Sasikanth Manne ,Zhangying Cai ,Alexander C Huang ,John Johnson ,Ryan P Staupe ,Bertram Bengsch ,Caiyue Xu ,Sixiang Yu ,Makoto Kurachi ,Ramin S Herati ,Laura A Vella ,Amy E Baxter ,Jennifer E Wu ,Omar Khan ,Jean-Christophe Beltra ,Josephine R Giles ,Erietta Stelekati ,Laura M McLane ,Chi Wai Lau ,Xiaolu Yang ,Shelley L Berger ,Golnaz Vahedi ,Hongkai Ji ,E John Wherry

Abstract

TCF-1 is a key transcription factor in progenitor exhausted CD8 T cells (Tex). Moreover, this Tex cell subset mediates responses to PD-1 checkpoint pathway blockade. However, the role of the transcription factor TCF-1 in early fate decisions and initial generation of Tex cells is unclear. Single-cell RNA sequencing (scRNA-seq) and lineage tracing identified a TCF-1+Ly108+PD-1+ CD8 T cell population that seeds development of mature Tex cells early during chronic infection. TCF-1 mediated the bifurcation between divergent fates, repressing development of terminal KLRG1Hi effectors while fostering KLRG1Lo Tex precursor cells, and PD-1 stabilized this TCF-1+ Tex precursor cell pool. TCF-1 mediated a T-bet-to-Eomes transcription factor transition in Tex precursors by promoting Eomes expression and drove c-Myb expression that controlled Bcl-2 and survival. These data define a role for TCF-1 in early-fate-bifurcation-driving Tex precursor cells and also identify PD-1 as a protector of this early TCF-1 subset.

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