| Literature DB >> 26201327 |
Mingjiang Xu1, Binxia Chang1, Stephanie Mathews1, Bin Gao2.
Abstract
Alcoholic liver disease (ALD) represents a spectrum of disorders, ranging from simple steatosis to severe alcoholic hepatitis and cirrhosis. The severe form of ALD comprises multiple problems in the liver, including inflammation, hepatocellular damage, fibrosis, and impaired liver regeneration, and likely requires combinational therapies. In this review, we discuss recently identified therapeutic targets that inhibit inflammation, ameliorate hepatocyte death, and promote liver repair in ALD, with a focus on our recent studies on the immunosuppressive drug prednisolone and the hepatoprotective cytokine interleukin-22. Clinical trials examining prednisolone plus interleukin-22 therapy for severe alcoholic hepatitis are currently under consideration.Entities:
Keywords: Ethanol; Inflammation; Interleukin-22; Liver; Prednisolone
Year: 2014 PMID: 26201327 PMCID: PMC5451265 DOI: 10.1007/s12072-014-9516-x
Source DB: PubMed Journal: Hepatol Int ISSN: 1936-0533 Impact factor: 6.047