TY - JOUR
T1 - Obstacles for T-lymphocytes in the tumour microenvironment
T2 - Therapeutic challenges, advances and opportunities beyond immune checkpoint
AU - Verma, Navin Kumar
AU - Wong, Brandon Han Siang
AU - Poh, Zhi Sheng
AU - Udayakumar, Aiswarya
AU - Verma, Ritu
AU - Goh, Ryan Kwang Jin
AU - Duggan, Shane P.
AU - Shelat, Vishalkumar G.
AU - Chandy, K. George
AU - Grigoropoulos, Nicholas Francis
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/9
Y1 - 2022/9
N2 - The tumour microenvironment (TME) imposes a major obstacle to infiltrating T-lymphocytes and suppresses their function. Several immune checkpoint proteins that interfere with ligand/receptor interactions and impede T-cell anti-tumour responses have been identified. Immunotherapies that block immune checkpoints have revolutionized the treatment paradigm for many patients with advanced-stage tumours. However, metabolic constraints and soluble factors that exist within the TME exacerbate the functional exhaustion of tumour-infiltrating T-cells. Here we review these multifactorial constraints and mechanisms – elevated immunosuppressive metabolites and enzymes, nutrient insufficiency, hypoxia, increased acidity, immense amounts of extracellular ATP and adenosine, dysregulated bioenergetic and purinergic signalling, and ionic imbalance - that operate in the TME and collectively suppress T-cell function. We discuss how scientific advances could help overcome the complex TME obstacles for tumour-infiltrating T-lymphocytes, aiming to stimulate further research for developing new therapeutic strategies by harnessing the full potential of the immune system in combating cancer.
AB - The tumour microenvironment (TME) imposes a major obstacle to infiltrating T-lymphocytes and suppresses their function. Several immune checkpoint proteins that interfere with ligand/receptor interactions and impede T-cell anti-tumour responses have been identified. Immunotherapies that block immune checkpoints have revolutionized the treatment paradigm for many patients with advanced-stage tumours. However, metabolic constraints and soluble factors that exist within the TME exacerbate the functional exhaustion of tumour-infiltrating T-cells. Here we review these multifactorial constraints and mechanisms – elevated immunosuppressive metabolites and enzymes, nutrient insufficiency, hypoxia, increased acidity, immense amounts of extracellular ATP and adenosine, dysregulated bioenergetic and purinergic signalling, and ionic imbalance - that operate in the TME and collectively suppress T-cell function. We discuss how scientific advances could help overcome the complex TME obstacles for tumour-infiltrating T-lymphocytes, aiming to stimulate further research for developing new therapeutic strategies by harnessing the full potential of the immune system in combating cancer.
KW - Immunotherapy
KW - Ionic checkpoint
KW - Tumor-infiltrating lymphocytes
KW - Tumor-interstitial fluid
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U2 - 10.1016/j.ebiom.2022.104216
DO - 10.1016/j.ebiom.2022.104216
M3 - Review article
C2 - 35986950
AN - SCOPUS:85135985273
SN - 2352-3964
VL - 83
JO - EBioMedicine
JF - EBioMedicine
M1 - 104216
ER -