Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Sep 6;34(9):467-474.
doi: 10.1093/intimm/dxac020.

The role of immune cells in the liver tumor microenvironment: an involvement of gut microbiota-derived factors

Affiliations
Review

The role of immune cells in the liver tumor microenvironment: an involvement of gut microbiota-derived factors

Tomonori Kamiya et al. Int Immunol. .

Abstract

More than 500 species of microbiota reside in the human intestine and coexist with humans, their host. Gut microbial metabolites and components are absorbed from the intestine and influence cells in the liver, including hepatocytes and stromal cells, such as liver sinusoidal endothelial cells, hepatic stellate cells, Kupffer cells, natural killer (NK) cells, NK T cells and other immune cells. This gut-originated axis to the liver is called the "gut-liver axis", which underscores the importance of the link between the gut and the liver. In this review, we discuss the gut microbial components and metabolites that affect cells in the liver, particularly in association with immune cells, and the related responses. We also highlight the mechanisms underlying gut microbiota-mediated liver carcinogenesis and discuss cancer prevention, including the recently clarified modulation of immune checkpoint inhibitor efficacy by the gut microbiota.

Keywords: deoxycholic acid (DCA); immune checkpoint inhibitor therapy; lipoteichoic acid (LTA); senescence-associated secretory phenotype (SASP).

PubMed Disclaimer

Publication types