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Impact of Antigen Presentation Mechanisms on Immune Response in Autoimmune Hepatitis

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.814155

关键词

autoimmune hepatitis; major histocompatibility complex class II; major histocompatibility complex class I; antigen processing and presentation; liver

资金

  1. Italian Association for Cancer Research (AIRC) through an Investigator Grant [20441]

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The liver is a tolerogenic organ that can induce immune tolerance against self-antigens. However, autoimmune liver diseases can disrupt this tolerance due to genetic predisposition, environmental factors, and imbalance in regulatory mechanisms. Liver cells, including conventional and unconventional antigen presenting cells (APCs), present self-antigens to T cells, leading to altered immune responses, liver injury, and inflammation. Understanding the impact of antigen presentation and the role of immune cells in liver inflammation could aid in the development of novel therapeutic strategies for autoimmune liver diseases.
The liver is a very tolerogenic organ. It is continually exposed to a multitude of antigens and is able to promote an effective immune response against pathogens and simultaneously immune tolerance against self-antigens. In spite of strong peripheral and central tolerogenic mechanisms, loss of tolerance can occur in autoimmune liver diseases, such as autoimmune hepatitis (AIH) through a combination of genetic predisposition, environmental factors, and an imbalance in immunological regulatory mechanisms. The liver hosts several types of conventional resident antigen presenting cells (APCs) such as dendritic cells, B cells and macrophages (Kupffer cells), and unconventional APCs including liver sinusoidal endothelial cells, hepatic stellate cells and hepatocytes. By standard (direct presentation and cross-presentation) and alternative mechanisms (cross-dressing and MHC class II-dressing), liver APCs presents self-antigen to naive T cells in the presence of costimulation leading to an altered immune response that results in liver injury and inflammation. Additionally, the transport of antigens and antigen:MHC complexes by trogocytosis and extracellular vesicles between different cells in the liver contributes to enhance antigen presentation and amplify autoimmune response. Here, we focus on the impact of antigen presentation on the immune response in the liver and on the functional role of the immune cells in the induction of liver inflammation. A better understanding of these key pathogenic aspects could facilitate the establishment of novel therapeutic strategies in AIH.

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