Autologous human monocyte-derived dendritic cells genetically modified to express melanoma antigens elicit primary cytotoxic T cell responses in vitro: enhancement by cotransfection of genes encoding the Th1-biasing cytokines IL-12 and IFN-alpha

J Immunol. 1998 Feb 1;160(3):1139-47.

Abstract

DNA-based immunization strategies designed to elicit cellular antitumor immunity offer an attractive alternative to protein- or peptide-based approaches. In the present study we have evaluated the feasibility of DNA vaccination for the induction of CTL reactivity to five different melanoma Ags in vitro. Cultured, monocyte-derived dendritic cells (DC) were transiently transfected with plasmid DNA encoding human MART-1/Melan-A, pMel-17/gp100, tyrosinase, MAGE-1, or MAGE-3 by particle bombardment and used to stimulate autologous PBMC responder T cells. CTL reactivity to these previously identified melanoma Ags was reproducibly generated after two or three stimulations with genetically modified DC. Co-ordinate transfection of two melanoma Ag cDNAs into DC promoted CTL responders capable of recognizing epitopes from both gene products. Coinsertion of genes encoding the Th1-biasing cytokines IL-12 or IFN-alpha consistently enhanced the magnitude of the resulting Ag-specific CTL reactivity. Importantly, DC transfected with a single melanoma Ag cDNA were capable of stimulating Ag-specific CTL reactivity restricted by multiple host MHC alleles, some of which had not been previously identified. These results support the inherent strengths of gene-based vaccine approaches that do not require prior knowledge of responder MHC haplotypes or of relevant MHC-restricted peptide epitopes. Given previous observations of in situ tumor HLA allele-loss variants, DC gene vaccine strategies may elicit a greater diversity of host therapeutic immunity, thereby enhancing the clinical utility and success of such approaches.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, Neoplasm / biosynthesis
  • Antigens, Neoplasm / genetics*
  • Cell Line
  • Cytotoxicity, Immunologic / genetics*
  • DNA, Complementary / genetics
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Epitopes, T-Lymphocyte / immunology
  • Humans
  • Immunophenotyping
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / genetics*
  • Interleukin-12 / biosynthesis
  • Interleukin-12 / genetics*
  • Luciferases / biosynthesis
  • Luciferases / genetics
  • MART-1 Antigen
  • Melanoma / immunology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Monocytes / immunology
  • Mutagenesis, Insertional / immunology
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology
  • Peptides / immunology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Th1 Cells / metabolism*
  • Transfection / immunology*
  • Tumor Cells, Cultured
  • Vaccines, DNA / immunology
  • gp100 Melanoma Antigen

Substances

  • Antigens, Neoplasm
  • DNA, Complementary
  • Epitopes, T-Lymphocyte
  • MAGEA3 protein, human
  • MART-1 Antigen
  • MLANA protein, human
  • Membrane Glycoproteins
  • Neoplasm Proteins
  • PMEL protein, human
  • Peptides
  • Vaccines, DNA
  • gp100 Melanoma Antigen
  • Interleukin-12
  • Interferon-gamma
  • Luciferases