Blockade of CTLA-4 promotes the development of effector CD8+ T lymphocytes and the therapeutic effect of vaccination with an attenuated protozoan expressing NY-ESO-1

Cancer Immunol Immunother. 2015 Mar;64(3):311-23. doi: 10.1007/s00262-014-1634-8. Epub 2014 Nov 18.

Abstract

The development of cancer immunotherapy has long been a challenge. Here, we report that prophylactic vaccination with a highly attenuated Trypanosoma cruzi strain expressing NY-ESO-1 (CL-14-NY-ESO-1) induces both effector memory and effector CD8(+) T lymphocytes that efficiently prevent tumor development. However, the therapeutic effect of such a vaccine is limited. We also demonstrate that blockade of Cytotoxic T Lymphocyte Antigen 4 (CTLA-4) during vaccination enhances the frequency of NY-ESO-1-specific effector CD8(+) T cells producing IFN-γ and promotes lymphocyte migration to the tumor infiltrate. As a result, therapy with CL-14-NY-ESO-1 together with anti-CTLA-4 is highly effective in controlling the development of an established melanoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Neoplasm / administration & dosage
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / parasitology
  • CTLA-4 Antigen / antagonists & inhibitors
  • CTLA-4 Antigen / immunology*
  • Cancer Vaccines / immunology*
  • Female
  • Humans
  • Immunotherapy / methods*
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / parasitology
  • Melanoma, Experimental / therapy*
  • Membrane Proteins / administration & dosage
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Trypanosoma cruzi / genetics
  • Trypanosoma cruzi / immunology

Substances

  • Antigens, Neoplasm
  • CTAG1B protein, human
  • CTLA-4 Antigen
  • CTLA4 protein, human
  • Cancer Vaccines
  • Membrane Proteins
  • Recombinant Proteins