败血症
CD8型
免疫系统
细胞毒性T细胞
免疫学
T细胞
肝损伤
细胞凋亡
医学
生物
药理学
生物化学
体外
作者
Zhengping Wei,Pingfei Li,Yao Yao,Hai Deng,Shengwu Yi,Cong Zhang,Han Wu,Xiuxiu Xie,Minghui Xia,Ran He,Xun Yang,Zhaohui Tang
标识
DOI:10.1016/j.clim.2018.04.010
摘要
In sepsis, the liver plays a crucial role in regulating immune responses and is also a target organ for immune-related injury. Despite the critical function of CD8+ T cells against opportunistic viral infections, the CD8 immune response in the liver during sepsis remains elusive. Here we found that Tim-3 is highly up-regulated in liver CD8+ T cells in a mouse cecal ligation and puncture model and in peripheral blood CD8+ T cells of human patients with sepsis. The expression of Tim-3 in liver CD8+ T cells displayed a bi-phasic pattern and deletion of Tim-3 led to reduction of CD8+ T cell apoptosis. Administration of α-lactose, a molecule with a similar structure to galactin-9, reduced Tim-3 expression and liver injury in sepsis. Our results demonstrate that targeting Tim-3 to boost CD8+ T cell immune response may offer an improved outcome in patients with sepsis.
科研通智能强力驱动
Strongly Powered by AbleSci AI