Liver-Mediated Adaptive Immune Tolerance

The liver is an immunologically tolerant organ that is uniquely equipped to limit hypersensitivity to food-derived antigens and bacterial products through the portal vein and can feasibly accept liver allografts. The adaptive immune response is a major branch of the immune system that induces organ/...

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Bibliographic Details
Published inFrontiers in immunology Vol. 10; p. 2525
Main Authors Zheng, Meijuan, Tian, Zhigang
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 05.11.2019
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Summary:The liver is an immunologically tolerant organ that is uniquely equipped to limit hypersensitivity to food-derived antigens and bacterial products through the portal vein and can feasibly accept liver allografts. The adaptive immune response is a major branch of the immune system that induces organ/tissue-localized and systematic responses against pathogens and tumors while promoting self-tolerance. Persistent infection of the liver with a virus or other pathogen typically results in tolerance, which is a key feature of the liver. The liver's immunosuppressive microenvironment means that hepatic adaptive immune cells become readily tolerogenic, promoting the death of effector cells and the "education" of regulatory cells. The above mechanisms may result in the clonal deletion, exhaustion, or inhibition of peripheral T cells, which are key players in the adaptive immune response. These tolerance mechanisms are believed to be responsible for almost all liver diseases. However, optimal protective adaptive immune responses may be achieved through checkpoint immunotherapy and the modulation of hepatic innate immune cells in the host. In this review, we focus on the mechanisms involved in hepatic adaptive immune tolerance, the liver diseases caused thereby, and the therapeutic strategies needed to overcome this tolerance.
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This article was submitted to Viral Immunology, a section of the journal Frontiers in Immunology
Edited by: Yuan Quan, Xiamen University, China
Reviewed by: Robert Thimme, University of Freiburg, Germany; Cai Zhang, Shandong University, China
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2019.02525