The hepatic microenvironment and regulatory T cells

•Regulatory T cells are crucial players in hepatic immune homeostasis.•Metabolites and microbial by-products contribute to the hepatic microenvironment.•The hepatic microenvironment influences the effector function of T cells.•Regulatory T cells could be utilised as a treatment for autoimmune liver...

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Veröffentlicht in:Cellular immunology 2020-11, Vol.357, p.104195-104195, Article 104195
Hauptverfasser: Osei-Bordom, Daniel, Bozward, Amber G., Oo, Ye Htun
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Sprache:eng
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Zusammenfassung:•Regulatory T cells are crucial players in hepatic immune homeostasis.•Metabolites and microbial by-products contribute to the hepatic microenvironment.•The hepatic microenvironment influences the effector function of T cells.•Regulatory T cells could be utilised as a treatment for autoimmune liver diseases. The human liver is regarded as a lymphoid organ that contributes to both local and systemic immune response. Intrahepatic immune cells including regulatory T cells (Tregs) reside in the hepatic microenvironment which is enriched with proinflammatory cytokines, chemokines and metabolites. In addition, the hepatic microenvironment has the unique ability to establish and maintain immune tolerance despite the continuous influx of the gut derived microbial products via the portal vein. Regulatory T cells play a crucial role in maintaining the hepatic tolerogenic state; however, the phenotypic stability, function and survival of Tregs in the inflamed liver microenvironment is still poorly understood. Despite this, Tregs immunotherapy remains as an appealing therapeutic option in autoimmune and immune mediated liver diseases. In order to advance cell therapy, it is important for us to further our understanding of the hepatic microenvironment, with the aim of developing ways to modify the hostile, inflamed environment to one which is more favourable. By doing so, T cell stability and function would be enhanced, resulting in improved clinical outcomes.
ISSN:0008-8749
1090-2163
DOI:10.1016/j.cellimm.2020.104195