Hurdle or thruster : Glucose metabolism of T cells in anti-tumour immunity

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved..

Glucose metabolism is essential for the activation, differentiation and function of T cells and proper glucose metabolism is required to maintain effective T cell immunity. Dysregulation of glucose metabolism is a hallmark of cancer, and the tumour microenvironment (TME2) can create metabolic barriers in T cells that inhibit their anti-tumour immune function. Targeting glucose metabolism is a promising approach to improve the capacity of T cells in the TME. The efficacy of common immunotherapies, such as immune checkpoint inhibitors (ICIs3) and adoptive cell transfer (ACT4), can be limited by T-cell function, and the treatment itself can affect T-cell metabolism. Therefore, understanding the relationship between immunotherapy and T cell glucose metabolism helps to achieve more effective anti-tumour therapy. In this review, we provide an overview of T cell glucose metabolism and how T cell metabolic reprogramming in the TME regulates anti-tumour responses, briefly describe the metabolic patterns of T cells during ICI and ACT therapies, which suggest possible synergistic strategies.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:1879

Enthalten in:

Biochimica et biophysica acta. Reviews on cancer - 1879(2024), 1 vom: 01. Jan., Seite 189022

Sprache:

Englisch

Beteiligte Personen:

Zhang, Sirui [VerfasserIn]
Zhang, Xiaozhen [VerfasserIn]
Yang, Hanshen [VerfasserIn]
Liang, Tingbo [VerfasserIn]
Bai, Xueli [VerfasserIn]

Links:

Volltext

Themen:

Adoptive cell transfer therapy
Glucose
Glucose metabolism
IY9XDZ35W2
Immune checkpoint
Journal Article
Metabolic reprogramming
Research Support, Non-U.S. Gov't
Review
T cell
Tumour microenvironment

Anmerkungen:

Date Completed 16.01.2024

Date Revised 27.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.bbcan.2023.189022

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM364842725