Targeting the arginine metabolic brake enhances immunotherapy for leukaemia

Int J Cancer. 2019 Oct 15;145(8):2201-2208. doi: 10.1002/ijc.32028. Epub 2019 Jan 11.

Abstract

Therapeutic approaches which aim to target Acute Myeloid Leukaemia through enhancement of patients' immune responses have demonstrated limited efficacy to date, despite encouraging preclinical data. Examination of AML patients treated with azacitidine (AZA) and vorinostat (VOR) in a Phase II trial, demonstrated an increase in the expression of Cancer-Testis Antigens (MAGE, RAGE, LAGE, SSX2 and TRAG3) on blasts and that these can be recognised by circulating antigen-specific T cells. Although the T cells have the potential to be activated by these unmasked antigens, the low arginine microenvironment created by AML blast Arginase II activity acts a metabolic brake leading to T cell exhaustion. T cells exhibit impaired proliferation, reduced IFN-γ release and PD-1 up-regulation in response to antigen stimulation under low arginine conditions. Inhibition of arginine metabolism enhanced the proliferation and cytotoxicity of anti-NY-ESO T cells against AZA/VOR treated AML blasts, and can boost anti-CD33 Chimeric Antigen Receptor-T cell cytotoxicity. Therefore, measurement of plasma arginine concentrations in combination with therapeutic targeting of arginase activity in AML blasts could be a key adjunct to immunotherapy.

Keywords: AML; CTAG; T; arginine; immunotherapy.

Publication types

  • Clinical Trial, Phase II
  • Randomized Controlled Trial

MeSH terms

  • Acute Disease
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Antigens, Neoplasm / metabolism*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Arginase / antagonists & inhibitors*
  • Arginase / blood
  • Arginase / metabolism
  • Arginine / blood*
  • Arginine / metabolism
  • Azacitidine / administration & dosage
  • Humans
  • Immunotherapy / methods
  • K562 Cells
  • Leukemia, Myeloid / immunology
  • Leukemia, Myeloid / metabolism
  • Leukemia, Myeloid / therapy*
  • Receptors, Chimeric Antigen / genetics
  • Receptors, Chimeric Antigen / metabolism
  • Sialic Acid Binding Ig-like Lectin 3 / immunology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology
  • Vorinostat / administration & dosage

Substances

  • Antigens, Neoplasm
  • CD33 protein, human
  • Receptors, Chimeric Antigen
  • Sialic Acid Binding Ig-like Lectin 3
  • Vorinostat
  • Arginine
  • ARG2 protein, human
  • Arginase
  • Azacitidine