Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
College of Pharmacy and Research Institute for Drug Development, Pusan National University, Busan, Republic of Korea.
Cell Mol Gastroenterol Hepatol. 2024;18(3):101352. doi: 10.1016/j.jcmgh.2024.04.009. Epub 2024 May 1.
Alcohol-associated hepatitis (AH) is an acute-on-chronic liver injury that occurs in patients with chronic alcohol-associated liver disease (ALD). Patients with severe AH have high short-term mortality and lack effective pharmacologic therapies. Inflammation is believed to be one of the key factors promoting AH progression and has been actively investigated as therapeutic targets over the last several decades, but no effective inflammatory targets have been identified so far. In this review, we discuss how inflammatory cells and the inflammatory mediators produced by these cells contribute to the development and progression of AH, with focus on neutrophils and macrophages. The crosstalk between inflammatory cells and liver nonparenchymal cells in the pathogenesis of AH is elaborated. We also deliberate the application of recent cutting-edge technologies in characterizing liver inflammation in AH. Finally, the potential therapeutic targets of inflammatory mediators for AH are briefly summarized.
酒精相关性肝炎(AH)是一种发生在慢性酒精相关性肝病(ALD)患者中的慢性加急性肝损伤。重度 AH 患者短期死亡率高,且缺乏有效的药物治疗。炎症被认为是促进 AH 进展的关键因素之一,在过去几十年中,它一直被积极研究作为治疗靶点,但迄今为止尚未确定有效的炎症靶点。在这篇综述中,我们讨论了炎症细胞及其产生的炎症介质如何促进 AH 的发生和发展,重点讨论了中性粒细胞和巨噬细胞。阐述了 AH 发病机制中炎症细胞与肝非实质细胞之间的串扰。我们还讨论了最近的前沿技术在 AH 肝炎症表征中的应用。最后,简要总结了炎症介质治疗 AH 的潜在治疗靶点。