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Immunological mechanisms and therapeutic targets of fatty liver diseases.脂肪性肝病的免疫机制和治疗靶点。
Cell Mol Immunol. 2021 Jan;18(1):73-91. doi: 10.1038/s41423-020-00579-3. Epub 2020 Dec 2.
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Itaconate controls the severity of pulmonary fibrosis.衣康酸盐可控制肺纤维化的严重程度。
Sci Immunol. 2020 Oct 23;5(52). doi: 10.1126/sciimmunol.abc1884.
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Hepatic macrophages in liver homeostasis and diseases-diversity, plasticity and therapeutic opportunities.肝脏稳态中的肝巨噬细胞:多样性、可塑性和治疗机会。
Cell Mol Immunol. 2021 Jan;18(1):45-56. doi: 10.1038/s41423-020-00558-8. Epub 2020 Oct 12.
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Transplantation of discarded livers following viability testing with normothermic machine perfusion.常温机器灌注下进行活力测试后废弃肝脏的移植。
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Niche-Specific Reprogramming of Epigenetic Landscapes Drives Myeloid Cell Diversity in Nonalcoholic Steatohepatitis.特定龛位的表观遗传景观重编程驱动非酒精性脂肪性肝炎中髓系细胞的多样性。
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Single-cell RNA sequencing reveals the heterogeneity of liver-resident immune cells in human.单细胞RNA测序揭示了人类肝脏驻留免疫细胞的异质性。
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Immunology. 2020 Jun;160(2):157-170. doi: 10.1111/imm.13193. Epub 2020 Apr 15.
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Single-Cell Transcriptomics Uncovers Zonation of Function in the Mesenchyme during Liver Fibrosis.单细胞转录组学揭示肝纤维化过程中间质功能的分区。
Cell Rep. 2019 Nov 12;29(7):1832-1847.e8. doi: 10.1016/j.celrep.2019.10.024.
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Landscape and Dynamics of Single Immune Cells in Hepatocellular Carcinoma.肝癌中单免疫细胞的景观和动态。
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Resolving the fibrotic niche of human liver cirrhosis at single-cell level.解析人肝硬化的纤维性龛位于单细胞水平。
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肝脏中的炎症过程:在稳态和病理学中的不同作用。

Inflammatory processes in the liver: divergent roles in homeostasis and pathology.

机构信息

School of Medicine, Trinity College Dublin, Dublin, Ireland.

Department of Biology, Kathleen Lonsdale Institute for Human Health Research, Maynooth University, Maynooth, Ireland.

出版信息

Cell Mol Immunol. 2021 Jun;18(6):1375-1386. doi: 10.1038/s41423-021-00639-2. Epub 2021 Apr 16.

DOI:10.1038/s41423-021-00639-2
PMID:33864004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8166849/
Abstract

The hepatic immune system is designed to tolerate diverse harmless foreign moieties to maintain homeostasis in the healthy liver. Constant priming and regulation ensure that appropriate immune activation occurs when challenged by pathogens and tissue damage. Failure to accurately discriminate, regulate, or effectively resolve inflammation offsets this balance, jeopardizing overall tissue health resulting from an either  overly tolerant or an overactive inflammatory response. Compelling scientific and clinical evidence links dysregulated hepatic immune and inflammatory responses upon sterile injury to several pathological conditions in the liver, particularly nonalcoholic steatohepatitis and ischemia-reperfusion injury. Murine and human studies have described interactions between diverse immune repertoires and nonhematopoietic cell populations in both physiological and pathological activities in the liver, although the molecular mechanisms driving these associations are not clearly understood. Here, we review the dynamic roles of inflammatory mediators in responses to sterile injury in the context of homeostasis and disease, the clinical implications of dysregulated hepatic immune activity and therapeutic developments to regulate liver-specific immunity.

摘要

肝脏免疫系统旨在耐受各种无害的外来物质,以维持健康肝脏的内稳态。持续的启动和调节确保在受到病原体和组织损伤的挑战时,适当的免疫激活发生。如果不能准确地区分、调节或有效地解决炎症,就会打破这种平衡,危及整体组织健康,导致过度耐受或过度活跃的炎症反应。令人信服的科学和临床证据表明,在无菌性损伤时肝脏免疫和炎症反应失调与肝脏的几种病理状况有关,特别是非酒精性脂肪性肝炎和缺血再灌注损伤。鼠类和人类研究描述了在肝脏的生理和病理活动中,各种免疫谱系与非造血细胞群体之间的相互作用,尽管驱动这些关联的分子机制尚不清楚。在这里,我们综述了炎症介质在无菌性损伤反应中的动态作用,包括在稳态和疾病中的作用、肝脏免疫活性失调的临床意义以及调节肝脏特异性免疫的治疗进展。