Human T cell receptor gammadelta cells recognize endogenous mevalonate metabolites in tumor cells

J Exp Med. 2003 Jan 20;197(2):163-8. doi: 10.1084/jem.20021500.

Abstract

T lymphocytes expressing the T cell receptor (TCR)-gammadelta recognize unknown antigens on tumor cells. Here we identify metabolites of the mevalonate pathway as the tumor ligands that activate TCR-gammadelta cells. In tumor cells, blockade of hydroxy-methylglutaryl-CoA reductase (HMGR), the rate limiting enzyme of the mevalonate pathway, prevents both accumulation of mevalonate metabolites and recognition by TCR-gammadelta cells. When metabolite accumulation is induced by overexpressing HMGR or by treatment with nitrogen-containing bisphosphonate drugs, tumor cells derived from many tissues acquire the capacity to stimulate the same TCR-gammadelta population. Accumulation of mevalonate metabolites in tumor cells is a powerful danger signal that activates the immune response and may represent a novel target of tumor immunotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / immunology
  • Breast Neoplasms / metabolism
  • Cells, Cultured
  • Female
  • Humans
  • Hydroxymethylglutaryl CoA Reductases / genetics
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Immunotherapy
  • Lymphocyte Activation
  • Mevalonic Acid / immunology*
  • Mevalonic Acid / metabolism*
  • Neoplasms / immunology*
  • Neoplasms / metabolism*
  • Neoplasms / therapy
  • Phosphorylation
  • Receptors, Antigen, T-Cell, gamma-delta / metabolism
  • T-Lymphocyte Subsets / immunology*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Receptors, Antigen, T-Cell, gamma-delta
  • Hydroxymethylglutaryl CoA Reductases
  • Mevalonic Acid