In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse

Br J Cancer. 2003 Jul 7;89(1):199-205. doi: 10.1038/sj.bjc.6601028.

Abstract

Parathyroid hormone-related protein (PTH-rP), a secreted protein produced by prostate carcinoma and other epithelial cancers, is considered a key agent for the development of bone metastases. We investigated the construct GC90/IRIV, composed of immunopotentiating reconstituted influenza virosomes (IRIV) containing PTH-rP gene plasmids (GC90), as a potential tool for human anticancer immunotherapy into humanised mice transgenic for HLA-A(*)02.01, the human-beta2 microglobulin, and the human CD8alpha molecule. Intranasal administration of GC90/IRIV resulted in the induction of a PTH-rP-specific multiepitope cytotoxic T-cell (CTL) response. Cytotoxic T cells derived from vaccinated mice were capable of lysing in vitro syngenic murine PTH-rP transfectants and human HLA-A((*))02.01(+)/PTH-rP(+) prostate carcinoma LNCaP cells as well. The immune response capacity and the absence of any sign of toxicity and/or autoimmunity in vivo suggest the GC90/IRIV vaccine as a valid tool for active specific immunotherapy of human cancers and metastases overexpressing PTH-rP.

MeSH terms

  • Animals
  • Cancer Vaccines*
  • Carcinoma / genetics
  • Carcinoma / immunology
  • Humans
  • Immunotherapy
  • Male
  • Mice
  • Mice, Transgenic*
  • Parathyroid Hormone-Related Protein
  • Peptide Fragments
  • Peptide Hormones / biosynthesis
  • Peptide Hormones / genetics*
  • Peptide Hormones / pharmacology
  • Plasmids
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / immunology
  • T-Lymphocytes, Cytotoxic
  • Tumor Cells, Cultured

Substances

  • Cancer Vaccines
  • PTHLH protein, human
  • Parathyroid Hormone-Related Protein
  • Peptide Fragments
  • Peptide Hormones