Fueling T-cell Antitumor Immunity: Amino Acid Metabolism Revisited.

Chenfeng Han, Minmin Ge, Ping-Chih Ho, Lianjun Zhang

Journal: Cancer immunology research 2022;9(12):1373-1382

PMID: 34716193

Abstract

T cells are the key players in eliminating malignant tumors. Adoptive transfer of tumor antigen-specific T cells and immune checkpoint blockade has yielded durable antitumor responses in the clinic, but not all patients respond initially and some that do respond eventually have tumor progression. Thus, new approaches to enhance the utility of immunotherapy are needed. T-cell activation and differentiation status are tightly controlled at the transcriptional, epigenetic, and metabolic levels. Amino acids are involved in multiple steps of T-cell antitumor immunity, including T-cell activation, proliferation, effector function, memory formation as well as functional exhaustion. In this review, we briefly discuss how amino acid metabolism is linked to T-cell fate decisions and summarize how amino acid deprivation or accumulation of certain amino acid metabolites within the tumor microenvironment diminishes T-cell functionality. Furthermore, we discuss potential strategies for immunotherapy via modulating amino acid metabolism either in T cells intrinsically or extrinsically to achieve therapeutic efficacy.

©2021 American Association for Cancer Research.

Address: CAMS Key Laboratory of Synthetic Biology Regulatory Elements, Institute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.; Suzhou Institute of Systems Medicine, Suzhou, China.; Department of Oncology, University of Lausanne, Lausanne, Switzerland. [email protected] [email protected].; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.; CAMS Key Laboratory of Synthetic Biology Regulatory Elements, Institute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. [email protected] [email protected].

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