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急性慢性肝衰竭的潜在治疗方法。

Potential therapies for acute-on-chronic liver failure.

作者信息

Morrison Maura A, Artru Florent, Trovato Francesca M, Triantafyllou Evangelos, McPhail Mark J

机构信息

Institute of Liver Studies, King's College Hospital, London, UK.

Department of Inflammation Biology, School of Immunology and Microbial Sciences, King's College London, London, UK.

出版信息

Liver Int. 2025 Mar;45(3):e15545. doi: 10.1111/liv.15545. Epub 2023 Mar 8.

DOI:10.1111/liv.15545
PMID:36800487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11815631/
Abstract

Acute-on-chronic liver failure (ACLF) is a syndrome that develops in approximately 30% of patients hospitalised with cirrhosis and is characterised by an acute decompensation of liver function associated with extra-hepatic organ failures and a high short-term mortality. At present, no specific therapies are available for ACLF, and current management is limited to treatment of the precipitating event and organ support. Given the high prevalence and high mortality of this severe liver disease, there is an urgent need for targeted treatments. There is increasing evidence of the important role played by systemic inflammation and immune dysfunction in the pathophysiology of ACLF and a better understanding of these immune processes is resulting in new therapeutic targets. The aim of this review is to present an overview of ongoing studies of potentially promising therapies and how they could be utilised in the management of ACLF.

摘要

慢加急性肝衰竭(ACLF)是一种综合征,约30%因肝硬化住院的患者会发生该综合征,其特征为肝功能急性失代偿,伴有肝外器官功能衰竭,且短期死亡率高。目前,尚无针对ACLF的特异性疗法,当前的治疗仅限于对诱发事件的处理和器官支持。鉴于这种严重肝病的高发病率和高死亡率,迫切需要有针对性的治疗方法。越来越多的证据表明全身炎症和免疫功能障碍在ACLF的病理生理学中发挥着重要作用,对这些免疫过程的更好理解正催生出新的治疗靶点。本综述的目的是概述正在进行的关于潜在有前景疗法的研究,以及这些疗法如何用于ACLF的管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3746/11815631/612aabbcf51b/LIV-45-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3746/11815631/612aabbcf51b/LIV-45-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3746/11815631/612aabbcf51b/LIV-45-0-g001.jpg

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本文引用的文献

1
Hyperammonaemia induces mitochondrial dysfunction and neuronal cell death.高氨血症会导致线粒体功能障碍和神经元细胞死亡。
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Combination of G-CSF and a TLR4 inhibitor reduce inflammation and promote regeneration in a mouse model of ACLF.粒细胞集落刺激因子(G-CSF)与Toll样受体4(TLR4)抑制剂联合使用可减轻急性肝衰竭(ACLF)小鼠模型中的炎症并促进再生。
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Organoids and regenerative hepatology.
Diagnostics (Basel). 2025 Mar 17;15(6):751. doi: 10.3390/diagnostics15060751.
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Acute and non-acute decompensation of liver cirrhosis (47/130).肝硬化的急性和非急性失代偿(47/130)
Liver Int. 2025 Mar;45(3):e15861. doi: 10.1111/liv.15861. Epub 2024 Mar 1.
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Acute decompensation of cirrhosis versus acute-on-chronic liver failure: What are the clinical implications?肝硬化急性失代偿与慢加急性肝衰竭:临床意义有何不同?
United European Gastroenterol J. 2024 Mar;12(2):194-202. doi: 10.1002/ueg2.12538. Epub 2024 Feb 20.
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Predicting the development of acute-on-chronic liver failure.预测慢加急性肝衰竭的发展。
United European Gastroenterol J. 2023 Nov;11(9):813-814. doi: 10.1002/ueg2.12482. Epub 2023 Nov 3.
7
Mechanisms and treatment approaches for ACLF.急性肝衰竭的发病机制与治疗方法
Liver Int. 2025 Mar;45(3):e15733. doi: 10.1111/liv.15733. Epub 2023 Sep 16.
类器官与再生肝脏学。
Hepatology. 2023 Jan 1;77(1):305-322. doi: 10.1002/hep.32583. Epub 2022 Jun 23.
4
Promises of microbiome-based therapies.基于微生物组的治疗方法的承诺。
J Hepatol. 2022 Jun;76(6):1379-1391. doi: 10.1016/j.jhep.2021.12.003.
5
The assessment of mesenchymal stem cells therapy in acute on chronic liver failure and chronic liver disease: a systematic review and meta-analysis of randomized controlled clinical trials.间充质干细胞治疗慢加急性肝衰竭和慢性肝病的评估:一项随机对照临床试验的系统评价和荟萃分析。
Stem Cell Res Ther. 2022 May 16;13(1):204. doi: 10.1186/s13287-022-02882-4.
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The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial.利福昔明对酒精性肝炎炎症和代谢的影响:一项随机临床试验。
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