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Inflammation in Alcohol-Associated Hepatitis: Pathogenesis and Therapeutic Targets.
Feng, Dechun; Hwang, Seonghwan; Guillot, Adrien; Wang, Yang; Guan, Yukun; Chen, Cheng; Maccioni, Luca; Gao, Bin.
Affiliation
  • Feng D; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland. Electronic address: dechun.feng@nih.gov.
  • Hwang S; College of Pharmacy and Research Institute for Drug Development, Pusan National University, Busan, Republic of Korea.
  • Guillot A; Department of Hepatology and Gastroenterology, Charité Universitätsmedizin Berlin, Berlin, Germany.
  • Wang Y; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
  • Guan Y; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
  • Chen C; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
  • Maccioni L; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
  • Gao B; Laboratory of Liver Diseases, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland. Electronic address: bgao@mail.nih.gov.
Cell Mol Gastroenterol Hepatol ; 18(3): 101352, 2024 May 01.
Article in En | MEDLINE | ID: mdl-38697358
ABSTRACT
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Mol Gastroenterol Hepatol Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Mol Gastroenterol Hepatol Year: 2024 Type: Article