| Literature DB >> 29689313 |
Zhengping Wei1, Pingfei Li1, Yao Yao2, Hai Deng2, Shengwu Yi2, Cong Zhang2, Han Wu2, Xiuxiu Xie1, Minghui Xia1, Ran He1, Xiang-Ping Yang1, Zhao-Hui Tang3.
Abstract
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.Entities:
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Year: 2018 PMID: 29689313 DOI: 10.1016/j.clim.2018.04.010
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969