[Antitumor effect of gene gun-mediated DNA vaccine pWRG-neu immunization in C57BL/6 mice]

Zhonghua Zhong Liu Za Zhi. 2003 Jul;25(4):320-4.
[Article in Chinese]

Abstract

Objective: To investigate the inhibitory effect of DNA vaccine immunization on neu-overexpressed melanoma growth in prophylactic treatment and anti-lung-metastasis experiments in C57BL/6 mice.

Methods: pcDNA-neu transfected into B16F10 with transfection reagent Fugene 6, neu-overexpressed cell clone B16F10-neu was selected with limited dilution method. The growth curve was drawn to analyse its proliferating character in vitro. With Helios gene gun system, DNA vaccine pWRG-neu was immunized to 8-week-old C57BL/6 mice in the shaved abdominal skin for 3 times at two-weekly interval. After immunization, the life span was analyzed. Using MTT assay, the cytolysis activity of the DNA immunized mice spleen cells was compared.

Results: One clone of neu-overexpressed B16F10-neu was selected and its proliferating character was the same as B16F10 and B16F10-pcDNA. In prophylactic, treatment and anti-lung-metastasis experiments, gene gun-mediated pWRG-neu immunization could exhibit antitumor effects. The growth and metastasis of neu-overexpressed melanoma was reduced dramatically. The spleen cells of the immuned mice showed cytotoxic T lymphocyte (CTL) activity.

Conclusion: Gene gun-mediated gene transfer is effective and practicable. DNA vaccine pWRG-neu is potent in preventing subsequent tumor cells challenge, inhibiting the tumor growth and metastasis.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biolistics
  • Cell Line, Tumor
  • Cytotoxicity, Immunologic
  • Genes, erbB-2*
  • Immunization
  • Lung Neoplasms / prevention & control*
  • Lung Neoplasms / secondary
  • Melanoma, Experimental / metabolism
  • Melanoma, Experimental / pathology
  • Melanoma, Experimental / therapy*
  • Mice
  • Mice, Inbred C57BL
  • Neoplasm Transplantation
  • Plasmids
  • Receptor, ErbB-2 / metabolism*
  • T-Lymphocytes, Cytotoxic / immunology
  • Vaccines, DNA*

Substances

  • Vaccines, DNA
  • Receptor, ErbB-2