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DOI: 10.1055/a-1957-6384
Regulation of Progression and Resolution of Liver Fibrosis by Immune Cells
Funding This study was supported in part by Japan Society for the Promotion of Science (JSPS) KAKENHI Grant-in-Aid (B) JP20H04129; Japan Agency for Medical Research and Development (AMED) 21fk0210096h0001.
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Abstract
The excessive accumulation of extracellular matrix proteins results in fibrosis—a condition implicated in several diseased conditions, such as nonalcoholic steatohepatitis, viral hepatitis, and autoimmune hepatitis. Despite its prevalence, direct and effective treatments for fibrosis are lacking, warranting the development of better therapeutic strategies. Accumulating evidence has shown that liver fibrosis—a condition previously considered irreversible—is reversible in specific conditions. Immune cells residing in or infiltrating the liver (e.g., macrophages) are crucial in the pathogenesis of fibrosis. Given this background, the roles and action mechanisms of various immune cells and their subsets in the progression and recovery of liver fibrosis, particularly concerning nonalcoholic steatohepatitis, are discussed in this review. Furthermore, the development of better therapeutic strategies based on stage-specific properties and using advanced techniques as well as the mechanisms underlying recovery are elaborated. In conclusion, we consider the review comprehensively provides the present achievements and future possibilities revolving around fibrosis treatment.
Keywords
liver fibrosis - immune cell regulation - macrophages - nonalcoholic steatohepatitis - tissue resident memory T cellsPublikationsverlauf
Accepted Manuscript online:
08. Oktober 2022
Artikel online veröffentlicht:
02. November 2022
© 2022. Thieme. All rights reserved.
Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA
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