Modified vaccinia virus Ankara for delivery of human tyrosinase as melanoma-associated antigen: induction of tyrosinase- and melanoma-specific human leukocyte antigen A*0201-restricted cytotoxic T cells in vitro and in vivo

Cancer Res. 1999 Oct 1;59(19):4955-63.

Abstract

Vaccination with tumor-associated antigens is a promising approach for cancer immunotherapy. Because the majority of these antigens are normal self antigens, they may require suitable delivery systems to promote their immunogenicity. A recombinant vector based on the modified vaccinia virus Ankara (MVA) was used for expression of human tyrosinase, a melanoma-specific differentiation antigen, and evaluated for its efficacy as an antitumor vaccine. Stable recombinant viruses (MVA-hTyr) were constructed that have deleted the selection marker lacZ and efficiently expressed human tyrosinase in primary human cells and cell lines. Tyrosinase-specific human CTLs were activated in vitro by MVA-hTyr-infected, HLA-A*0201-positive human dendritic cells. Importantly, an efficient tyrosinase- and melanoma-specific CTL response was induced in vitro using MVA-hTyr-infected autologous dendritic cells as activators for peripheral blood mononuclear cells derived from HLA-A*0201-positive melanoma patients despite prior vaccination against smallpox. Immunization of HLA-A*0201/Kb transgenic mice with MVA-hTyr induced A*0201-restricted CTLs specific for the human tyrosinase-derived peptide epitope 369-377. These in vivo primed CTLs were of sufficiently high avidity to recognize and lyse human melanoma cells, which present the endogenously processed tyrosinase peptide in the context of A*0201. Tyrosinase-specific CTL responses were significantly augmented by repeated vaccination with MVA-hTyr. These findings demonstrate that HLA-restricted CTLs specific for human tumor-associated antigens can be efficiently generated by immunization with recombinant MVA vaccines. The results are an essential basis for MVA-based vaccination trials in cancer patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Dendritic Cells / immunology
  • Dendritic Cells / physiology
  • Enzyme Induction
  • Genetic Markers
  • Genetic Vectors*
  • HLA-A Antigens / immunology*
  • Humans
  • Lymphocyte Activation
  • Melanoma / immunology*
  • Mice
  • Mice, Transgenic
  • Monophenol Monooxygenase / biosynthesis*
  • Monophenol Monooxygenase / genetics*
  • Recombinant Fusion Proteins / biosynthesis
  • Sequence Deletion
  • Smallpox Vaccine
  • T-Lymphocytes, Cytotoxic / immunology*
  • Transfection
  • Vaccinia virus*

Substances

  • Genetic Markers
  • HLA-A Antigens
  • Recombinant Fusion Proteins
  • Smallpox Vaccine
  • Monophenol Monooxygenase