Presentation of prostate tumor antigens by dendritic cells stimulates T-cell proliferation and cytotoxicity

Prostate. 1996 Jan;28(1):65-9. doi: 10.1002/(SICI)1097-0045(199601)28:1<65::AID-PROS9>3.0.CO;2-N.

Abstract

Dendritic cells (DCs) are "professional" antigen-presenting cells capable of stimulating T-cell proliferation and cytotoxicity when loaded with and presenting specific antigens, including tumor antigens. We demonstrated the stimulation of an autologous cytotoxic T-cell response elicited by DC loaded with autologous tumor cell lysate derived from primary prostate tumor. A candidate tumor antigen is prostate-specific membrane antigen (PSMA), which is overexpressed in prostate cancer patients. We identified a HLA-A2 motif in PSMA, isolated patient DC, loaded peptide into DC, and stimulated autologous T cells to proliferate. The ability to use DC for presentation of either tumor or peptide antigen in an HLA-restricted fashion in order to stimulate T-cell proliferation and cytotoxicity demonstrates the potential of this technology for development of a prostate cancer vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antigens, Neoplasm / analysis
  • Antigens, Neoplasm / pharmacology*
  • Antigens, Surface / analysis
  • Antigens, Surface / pharmacology*
  • Cell Division / drug effects
  • Cytotoxicity, Immunologic / drug effects*
  • Dendritic Cells / immunology*
  • Dendritic Cells / physiology
  • Glutamate Carboxypeptidase II
  • HLA-A Antigens
  • Humans
  • Immunotherapy, Active
  • Male
  • Molecular Sequence Data
  • Prostatic Neoplasms / immunology*
  • Prostatic Neoplasms / pathology
  • Prostatic Neoplasms / therapy
  • T-Lymphocytes / drug effects*
  • Tumor Cells, Cultured

Substances

  • Antigens, Neoplasm
  • Antigens, Surface
  • HLA-A Antigens
  • FOLH1 protein, human
  • Glutamate Carboxypeptidase II