Survival of the fittest: Cancer challenges T cell metabolism

Davide G Franchina1, Feng He2, Dirk Brenner3

  • 1Department of Infection and Immunity, Experimental and Molecular Immunology, Luxembourg Institute of Health, 29, rue Henri Koch, L-4354 Esch-sur-Alzette, Luxembourg.

Cancer Letters
|October 28, 2017
PubMed

Insights

Tumor microenvironments impair T cells by altering their metabolism. Understanding these metabolic changes is key for developing effective cancer immunotherapies and improving T cell function against tumors.

Area of Science:

  • Immunology
  • Cancer Biology
  • Metabolic Research

Background:

  • T cells are crucial for anti-tumor immunity but are often impaired within the tumor microenvironment.
  • Tumors evade immune surveillance by manipulating the tumor microenvironment, leading to weakened anti-tumor responses.
  • Nutrient availability and consumption critically influence T cell differentiation and effector functions.

Purpose of the Study:

  • To discuss T cell fates during anti-tumor immune responses.
  • To explore how tumor microenvironment signals influence T cell metabolism.
  • To highlight the impact of metabolic alterations on T cell function and longevity.

Main Methods:

  • Literature review and discussion of existing research on T cell metabolism in the tumor microenvironment.
  • Analysis of nutrient competition between cancer cells and tumor-infiltrating lymphocytes.
  • Examination of the role of regulatory T cells (Treg) in immune privilege within tumors.

Main Results:

  • Tumor microenvironments reprogram T cell metabolism, impairing their anti-tumor functions.
  • Cancer cells can outcompete T cells for essential nutrients, further compromising immune responses.
  • Immune checkpoint inhibitors (PD1, CTLA4) show partial metabolic remodeling, paving the way for metabolic reprogramming therapies.

Conclusions:

  • T cell metabolism is a critical determinant of anti-tumor immunity.
  • Targeting metabolic pathways within the tumor microenvironment offers a promising therapeutic strategy.
  • Further research into metabolic reprogramming can enhance T cell longevity and effector functions for cancer treatment.

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