Ligand-Receptor Interactions of Galectin-9 and VISTA Suppress Human T Lymphocyte Cytotoxic Activity

Front Immunol. 2020 Nov 20:11:580557. doi: 10.3389/fimmu.2020.580557. eCollection 2020.

Abstract

Acute myeloid leukemia (AML), a blood/bone marrow cancer, is a severe and often fatal malignancy. AML cells are capable of impairing the anti-cancer activities of cytotoxic lymphoid cells. This includes the inactivation of natural killer (NK) cells and killing of T lymphocytes. Here we report for the first time that V-domain Ig-containing suppressor of T cell activation (VISTA), a protein expressed by T cells, recognizes galectin-9 secreted by AML cells as a ligand. Importantly, we found that soluble VISTA released by AML cells enhances the effect of galectin-9, most likely by forming multiprotein complexes on the surface of T cells and possibly creating a molecular barrier. These events cause changes in the plasma membrane potential of T cells leading to activation of granzyme B inside cytotoxic T cells, resulting in apoptosis.

Keywords: Galectin-9; NK cells; T cells; VISTA; acute myeloid leukemia; immune escape.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm
  • Apoptosis
  • B7 Antigens / metabolism*
  • Cytotoxicity, Immunologic
  • Galectins / metabolism*
  • Granzymes / metabolism
  • Humans
  • Immunosuppression Therapy
  • Ligands
  • Membrane Potentials
  • Protein Binding
  • Protein Multimerization
  • T-Lymphocytes, Cytotoxic / immunology*
  • THP-1 Cells
  • Tumor Escape

Substances

  • Antigens, Neoplasm
  • B7 Antigens
  • Galectins
  • LGALS9 protein, human
  • Ligands
  • VSIR protein, human
  • Granzymes