Recombinant modified vaccinia virus ankara (MVA) expressing wild-type human p53 induces specific antitumor CTL expansion

Cancer Invest. 2011 Oct;29(8):501-10. doi: 10.3109/07357907.2011.606248. Epub 2011 Aug 15.

Abstract

The p53 gene product is an attractive target for tumor immunotherapy. The present study aims to understand the potential of MVAp53 vaccine to induce expansion of p53-specific cytotoxic T lymphocyte ex vivo in cancer patients. The result indicated that 14 of 23 cancer patients demonstrated p53-specific IFN-γ production, degranulation, cell proliferation, and lysis of p53 overexpressed human tumor cell lines. These experiments show that MVAp53 stimulation has the potential to induce the expansion of p53-specific cytotoxic T lymphocyte from the memory T cell repertoire. The data suggest that MVAp53 vaccine is an ideal candidate for cancer immunotherapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cancer Vaccines / immunology*
  • Cell Degranulation
  • Cell Line, Tumor
  • Cell Proliferation
  • Cytotoxicity, Immunologic
  • Female
  • Humans
  • Interferon-gamma / biosynthesis
  • Male
  • Middle Aged
  • T-Lymphocytes, Cytotoxic / cytology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Tumor Suppressor Protein p53 / immunology*
  • Vaccines, Synthetic / immunology
  • Vaccinia virus / genetics

Substances

  • Cancer Vaccines
  • MVAp53 vaccine
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Vaccines, Synthetic
  • Interferon-gamma