Tumor expression of 4-1BB ligand sustains tumor lytic T cells

Cancer Biol Ther. 2003 Sep-Oct;2(5):579-86. doi: 10.4161/cbt.2.5.545.

Abstract

Inadequate costimulation by solid tumors is generally believed to induce immune tolerance during primary tumor growth. We looked for tumor-specific immunity vs. tolerance in patients with Ewing's sarcoma. Circulating T cells from patients with progressively growing Ewing's tumors displayed MHC restricted tumor-induced proliferation and robust tumor lysis. Tumor-reactive T cells reside within the memory CD3+CD8+ subset and are CD28-/4-1BB+. Autologous Ewing's tumors expressed 4-1BBL, and tumor-induced T cell proliferation and activation required costimulation by 4-1BBL. Stimulation of PBL with anti-CD3/4-1BBL, but not anti-CD3/anti-CD28 induced tumor lytic effectors. Similarly, in a xenograft model, anti-CD3/4-1BBL expanded T cells controlled primary growth and prevented metastasis of autologous tumors while nonactivated and anti-CD3/anti-CD28 activated CD8+ cells did not. These results question prevailing models of tumor induced tolerance accompanying progressive tumor growth; rather, we show coexistence of progressive tumor growth and anti-tumor immunity, with costimulation provided by the tumor itself. They further demonstrate a potential new therapeutic role for 4-1BBL mediated costimulation in expanding tumor reactive CTLs for use in the adoptive immunotherapy of cancer.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-1BB Ligand
  • Adolescent
  • Adult
  • Animals
  • Bone Neoplasms / immunology*
  • Bone Neoplasms / prevention & control
  • CD28 Antigens / metabolism
  • CD3 Complex / metabolism
  • CD8 Antigens / metabolism
  • Dendritic Cells / immunology
  • Female
  • Humans
  • Ligands
  • Lymphocyte Activation*
  • Lymphocytes, Tumor-Infiltrating / metabolism
  • Male
  • Mice
  • Mice, SCID
  • Receptors, Antigen, T-Cell / metabolism
  • Sarcoma, Ewing / immunology*
  • Sarcoma, Ewing / prevention & control
  • T-Lymphocytes / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • 4-1BB Ligand
  • CD28 Antigens
  • CD3 Complex
  • CD8 Antigens
  • Ligands
  • Receptors, Antigen, T-Cell
  • TNFSF9 protein, human
  • Tnfsf9 protein, mouse
  • Tumor Necrosis Factor-alpha