Regulation of T cell antitumor immune response by tumor induced metabolic stress

Adaptive T cell immune response is essential for tumor growth control. The efficacy of immune checkpoint inhibitors is regulated by intratumoral immune response. The tumor microenvironment has a major role in adaptive immune response tuning. Tumor cells generate a particular metabolic environment in...

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Main Authors: Fanny Chalmin, Mélanie Bruchard, Frederique Vegran, Francois Ghiringhelli
Format: Article
Language:English
Published: Shared Science Publishers OG 2018-11-01
Series:Cell Stress
Subjects:
Online Access:http://www.cell-stress.com/researcharticles/2019a-chalmin-cell-stress/
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spelling doaj-1fe5e2a3393c487d8f27ea2c7894fda82020-11-25T01:07:50ZengShared Science Publishers OGCell Stress2523-02042018-11-013191810.15698/cst2019.01.171Regulation of T cell antitumor immune response by tumor induced metabolic stressFanny Chalmin0Mélanie Bruchard1Frederique Vegran2Francois Ghiringhelli3Cancer Biology Research Platform, Centre Georges-François Leclerc, Dijon, France.Cancer Biology Research Platform, Centre Georges-François Leclerc, Dijon, France.Cancer Biology Research Platform, Centre Georges-François Leclerc, Dijon, France.Cancer Biology Research Platform, Centre Georges-François Leclerc, Dijon, France.Adaptive T cell immune response is essential for tumor growth control. The efficacy of immune checkpoint inhibitors is regulated by intratumoral immune response. The tumor microenvironment has a major role in adaptive immune response tuning. Tumor cells generate a particular metabolic environment in comparison to other tissues. Tumors are characterized by glycolysis, hypoxia, acidosis, amino acid depletion and fatty acid metabolism modification. Such metabolic changes promote tumor growth, impair immune response and lead to resistance to therapies. This review will detail how these modifications strongly affect CD8 and CD4 T cell functions and impact immunotherapy efficacy.http://www.cell-stress.com/researcharticles/2019a-chalmin-cell-stress/antitumor immmunitymetabolic stressacidosishypoxiaamino acidsfatty acidT cells
collection DOAJ
language English
format Article
sources DOAJ
author Fanny Chalmin
Mélanie Bruchard
Frederique Vegran
Francois Ghiringhelli
spellingShingle Fanny Chalmin
Mélanie Bruchard
Frederique Vegran
Francois Ghiringhelli
Regulation of T cell antitumor immune response by tumor induced metabolic stress
Cell Stress
antitumor immmunity
metabolic stress
acidosis
hypoxia
amino acids
fatty acid
T cells
author_facet Fanny Chalmin
Mélanie Bruchard
Frederique Vegran
Francois Ghiringhelli
author_sort Fanny Chalmin
title Regulation of T cell antitumor immune response by tumor induced metabolic stress
title_short Regulation of T cell antitumor immune response by tumor induced metabolic stress
title_full Regulation of T cell antitumor immune response by tumor induced metabolic stress
title_fullStr Regulation of T cell antitumor immune response by tumor induced metabolic stress
title_full_unstemmed Regulation of T cell antitumor immune response by tumor induced metabolic stress
title_sort regulation of t cell antitumor immune response by tumor induced metabolic stress
publisher Shared Science Publishers OG
series Cell Stress
issn 2523-0204
publishDate 2018-11-01
description Adaptive T cell immune response is essential for tumor growth control. The efficacy of immune checkpoint inhibitors is regulated by intratumoral immune response. The tumor microenvironment has a major role in adaptive immune response tuning. Tumor cells generate a particular metabolic environment in comparison to other tissues. Tumors are characterized by glycolysis, hypoxia, acidosis, amino acid depletion and fatty acid metabolism modification. Such metabolic changes promote tumor growth, impair immune response and lead to resistance to therapies. This review will detail how these modifications strongly affect CD8 and CD4 T cell functions and impact immunotherapy efficacy.
topic antitumor immmunity
metabolic stress
acidosis
hypoxia
amino acids
fatty acid
T cells
url http://www.cell-stress.com/researcharticles/2019a-chalmin-cell-stress/
work_keys_str_mv AT fannychalmin regulationoftcellantitumorimmuneresponsebytumorinducedmetabolicstress
AT melaniebruchard regulationoftcellantitumorimmuneresponsebytumorinducedmetabolicstress
AT frederiquevegran regulationoftcellantitumorimmuneresponsebytumorinducedmetabolicstress
AT francoisghiringhelli regulationoftcellantitumorimmuneresponsebytumorinducedmetabolicstress
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