Blimp-1 represses CD8 T cell expression of PD-1 using a feed-forward transcriptional circuit during acute viral infection

被引:122
|
作者
Lu, Peiyuan
Youngblood, Benjamin A.
Austin, James W.
Mohammed, Ata Ur Rasheed
Butler, Royce
Ahmed, Rafi
Boss, Jeremy M. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2014年 / 211卷 / 03期
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; VIRUS-INFECTION; PROGRAMMED DEATH-1; UP-REGULATION; PLASMA-CELLS; ANTIGEN; MEMORY; DIFFERENTIATION; EXHAUSTION; SAFETY;
D O I
10.1084/jem.20130208
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Programmed cell death 1 (PD-1) is an inhibitory immune receptor that regulates T cell function, yet the molecular events that control its expression are largely unknown. We show here that B lymphocyte-induced maturation protein 1 (Blimp-1)-deficient CD8 T cells fail to repress PD-1 during the early stages of CD8 T cell differentiation after acute infection with lymphocytic choriomeningitis virus (LCMV) strain Armstrong. Blimp-1 represses PD-1 through a feed-forward repressive circuit by regulating PD-1 directly and by repressing NFATc1 expression, an activator of PD-1 expression. Blimp-1 binding induces a repressive chromatin structure at the PD-1 locus, leading to the eviction of NFATc1 from its site. These data place Blimp-1 at an important phase of the CD8 T cell effector response and provide a molecular mechanism for its repression of PD-1.
引用
收藏
页码:515 / 527
页数:13
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