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Related Concept Videos

T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
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Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
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Metabolic Reprogramming and CD8+ T-Cell Exhaustion During Chronic HBV Infection.

Haohao Li1, Weiwei Mu2, Alison Zhao3

  • 1State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Institute of Immunopharmaceutical Sciences, School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong, China.

Liver International : Official Journal of the International Association for the Study of the Liver
|October 17, 2025
PubMed
Summary
This summary is machine-generated.

Hepatitis B virus (HBV) infection alters liver cell and T-cell metabolism, leading to immune exhaustion. Metabolic interventions show promise for treating chronic HBV infection by restoring immune responses.

Keywords:
CD8+ T‐cellschronic hepatitis Bhepatocytesimmunometabolismmetabolic reprogramming

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Area of Science:

  • Hepatology
  • Immunology
  • Virology

Background:

  • Hepatitis B virus (HBV) infects hepatocytes, altering the liver microenvironment.
  • HBV infection induces metabolic reprogramming in CD8+ T-cells, contributing to immune exhaustion.

Purpose of the Study:

  • To review metabolic characteristics of hepatocytes and T-cells during HBV infection.
  • To discuss the link between CD8+ T-cell exhaustion and metabolic reprogramming.
  • To highlight therapeutic potential of metabolic approaches for chronic HBV.

Main Methods:

  • Literature review of recent advances in HBV metabolism and immunology.
  • Analysis of the relationship between metabolic reprogramming and T-cell exhaustion.
  • Evaluation of metabolic interventions for HBV treatment.

Main Results:

  • HBV directly regulates hepatocyte metabolism, impacting the liver immune microenvironment.
  • Metabolic reprogramming in T-cells is a key driver of exhaustion during chronic HBV infection.
  • Intercellular metabolite exchange influences HBV persistence and antiviral immunity.

Conclusions:

  • Metabolic reprogramming is central to HBV pathogenesis and immune evasion.
  • Targeting host cell metabolism offers a promising therapeutic strategy for chronic HBV infection.
  • Metabolic interventions may restore antiviral immunity and potentially cure HBV.