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.
Copyright © 2018 Elsevier Inc. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Apoptosis / drug effects*
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Apoptosis / genetics
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Apoptosis / immunology
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CD8-Positive T-Lymphocytes / drug effects*
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CD8-Positive T-Lymphocytes / immunology
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CD8-Positive T-Lymphocytes / metabolism
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Cells, Cultured
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Cytokines / genetics
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Cytokines / immunology
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Cytokines / metabolism
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Gene Expression / drug effects
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Gene Expression / immunology
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Hepatitis / genetics
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Hepatitis / immunology
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Hepatitis / prevention & control
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Hepatitis A Virus Cellular Receptor 2 / antagonists & inhibitors*
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Hepatitis A Virus Cellular Receptor 2 / genetics
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Hepatitis A Virus Cellular Receptor 2 / immunology
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Humans
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Lactose / administration & dosage
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Lactose / pharmacology*
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Leukocytes, Mononuclear / drug effects
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Leukocytes, Mononuclear / immunology
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Leukocytes, Mononuclear / metabolism
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Liver / drug effects*
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Liver / metabolism
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Liver / pathology
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Mice, Inbred C57BL
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Sepsis / genetics
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Sepsis / immunology*
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Sepsis / metabolism
Substances
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Cytokines
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Havcr2 protein, mouse
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Hepatitis A Virus Cellular Receptor 2
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Lactose