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Updated: Feb 20, 2026

Author Spotlight: Transmitochondrial Cybrid Generation Using Cancer Cell Lines
Published on: March 17, 2023
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.
Abstract:
T cells represent the major contributors to antitumor-specific immunity among the tumor-infiltrating lymphocytes. However, tumors acquire ways to evade immunosurveillance and anti-tumor responses are too weak to eradicate the disease. T cells are often functionally impaired as a result of interaction with, or signals from, transformed cells and the tumor microenvironment, including stromal cells. Among these, nutrients use and consumption is critically important for the control of differentiation and effector mechanisms of T cells. Moreover, Treg cells-skewing conditions often coexist within the cancer milieu, which sustains the notion of immune privileged tumors. Additionally, cancer cells contend with tumor infiltrating lymphocytes for nutrients and can outcompete the immune response. PD1- and CTLA-based immunotherapies partially remodel cell metabolism leading the way to clinical approaches of metabolic reprogramming for therapeutic purposes. Here we shortly discuss T cell fates during anti-tumor immune responses and how signals within tumor microenvironment influence T cell metabolism, altering functions and longevity of the cell.
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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