Published online Jan 28, 2005. doi: 10.3748/wjg.v11.i4.557
Revised: December 16, 2003
Accepted: March 16, 2004
Published online: January 28, 2005
AIM: To find a novel antigen (Ag) presentation strategy to improve the immune responses induced by dendritic cell (DC) vaccine expressing hepatitis C virus (HCV) core antigen (pcDNA 3HCV C-Fc) in Balb/c mice (H-2d).
METHODS: pcDNA 3HCV C-Fc plasmid and eukaryotic expression vector pcDNA3 were injected into mice sc. Immune responses to pcDNA 3HCV C-Fc were studied. Meanwhile the effect of pcDNA 3HCV C-Fc on anti-translated subcutaneous tumor of SP2/0 cells stably expressing HCV C Ag (SP2/0-HCV C-FC) was also studied. Anti-HCV C in serum was detected by enzyme-linked immunoadsordent assay (ELISA) and HCV specific cytotoxic T lymphocyte (CTL) activity was measured by LDH release assay. After 3 wk of DNA immunization, the cells of SP2/0-HCV C-FC were inoculated into mice subcutaneously and tumor growth was measured every 5 d. The survival rate and living time of mice were also calculated.
RESULTS: After 4 wk of DC immunization, the A450 nm values of sera in mice immunized with pcDNA 3HCV C-Fc-DC and pcDNA3-DC were 0.56±0.17 and 0.12±0.03 respectively. The antibody titres in mice codeliveried with pcDNA 3HCV C-Fc with DC were significantly higher than those of mice injected with pcDNA3-DC. The HCV specific CTL activities in mice coinjected with DC and pcDNA 3HCV C-Fc or empty expression vectors were(73.2±3.1) % and (24.4±8.8) % , which were significantly higher than those of mice injected with water. The DC vaccine could evidently inhibit tumor growth, prolong the survival time of mice and improve the survival rate of mice and these effects could be improved by HCV C-Fc (pcDNA 3HCV C-Fc) gene codelivered.
CONCLUSION: DC vaccine has a strong antigenicity in humoral and cellular immunities, which can be promoted by transduced pcDNA 3HCV C-Fc expressing HCV C or Fc. Thus, pcDNA 3HCV C-Fc-transduced DCs may be a promising candidate for a CTL-based vaccine against HCV.