免疫系统
CD8型
细胞毒性T细胞
PI3K/AKT/mTOR通路
细胞生物学
生物
存储单元
机制(生物学)
糖酵解
T细胞
免疫学
新陈代谢
信号转导
生物化学
体外
量子力学
认识论
物理
哲学
电压
晶体管
作者
Jingjing Yan,Mingbin Liu,Jianqing Xu
出处
期刊:Chinese journal of microbiology and immunology
日期:2019-02-28
卷期号:39 (2): 145-149
标识
DOI:10.3760/cma.j.issn.0254-5101.2019.02.012
摘要
CD8+ T cells are critical immune cells protecting the body against infection and cancer. Long-lived memory CD8+ T cells formed in a prior infection can reproduce to mount a faster and stronger immune response at a second encounter with the cognate antigen. The activation, clonal expansion and response of T cells are energetically demanding processes tightly coupled in cellular metabolism. Meanwhile, changes in cellular metabolism could also affect the development of memory T cells following acute infection. In this review, we discussed the current understanding of the mechanism by which glycometabolic pathways manipulate the differentiation of memory CD8+ T cells in order to provide reference for improving vaccine development and cancer treatment.
Key words:
Glycometabolism; Glycolysis; mTOR; Memory T cell
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