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REVIEW article

Front. Immunol.

Sec. Cancer Immunity and Immunotherapy

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1696113

The Impact of Metabolic Reprogramming in Hepatocellular Carcinoma on T Cell

Provisionally accepted
Dong-Xu  LiaoDong-Xu Liao1Xiang  AnXiang An1Gui-Xiang  HuangGui-Xiang Huang2*Tong-Ling  YuanTong-Ling Yuan3*
  • 1Department of Hepatobiliary and Pancreatic Surgery, Sichuan Provincial People's Hospital, school of medicine, University of Electronic Science and Technology of China, Chengdu, China
  • 2Department of Emergency surgery, Sichuan Provincial People’s Hospital, school of medicine, University of Electronic Science and Technology of China, Chengdu, China
  • 3General Practice Center, Sichuan Provincial People's Hospital, school of medicine, University of Electronic Science and Technology of China, Chengdu, China

The final, formatted version of the article will be published soon.

Hepatocellular carcinoma (HCC) is the predominant type of liver cancer, characterized by high incidence and mortality rates. Despite advancements in surgical and systemic therapies, the prognosis remains poor due to the asymptomatic nature of early-stage HCC. Metabolic reprogramming in HCC cells usually creates an immunosuppressive tumor microenvironment (TME), thereby impeding T cell-mediated antitumor immunity. This review focuses on the metabolic reprogramming patterns in HCC, their impact on T cell function, and the potential of metabolic-immune targeted combination therapies. We emphasize that nutrient competition and the accumulation of inhibitory metabolites are key mechanisms underlying T cell suppression in the TME. This review provides an update on the complex metabolic-immune interactions and helps to identify new therapeutic targets to improve the efficacy of immunotherapy for HCC.

Keywords: hepatocellular carcinoma (HCC), metabolic reprogramming, Tumormicroenvironment (TME), T cell-mediated antitumor immunity, Metabolic-immune targetedcombination therapies

Received: 31 Aug 2025; Accepted: 21 Oct 2025.

Copyright: © 2025 Liao, An, Huang and Yuan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Gui-Xiang Huang, huangguixiang1989@126.com
Tong-Ling Yuan, qingxinbiluochun23@163.com

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