Phase 1 safety and immune response studies of a DNA vaccine encoding hepatitis B surface antigen delivered by a gene delivery device

Vaccine. 1999 Jul 16;17(22):2826-9. doi: 10.1016/s0264-410x(99)00094-8.

Abstract

This study was designed to determine the safety and immunogenicity in volunteers of a DNA vaccine consisting of a plasmid encoding hepatitis B surface antigen delivered by the PowderJect XR1 gene delivery system into human skin. Seven healthy adult volunteers received two immunizations at one of three forces of delivery on day 0 and 56. The vaccine was well tolerated. One of six seronegative volunteers developed high titers of persistent HBsAb after a single immunization. In retrospect, this volunteer may have had previous exposure to hepatitis B. Our study suggests that the hepatitis B DNA vaccine given by this gene delivery system may induce a booster response, but the vaccine at the extremely low DNA dose used (0.25 microg) did not induce primary immune responses.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Viral / blood
  • DNA, Viral / adverse effects
  • DNA, Viral / therapeutic use
  • Drug Delivery Systems / adverse effects
  • Hepatitis B / immunology*
  • Hepatitis B / prevention & control*
  • Hepatitis B Surface Antigens / genetics*
  • Hepatitis B Surface Antigens / immunology*
  • Hepatitis B Vaccines / adverse effects
  • Hepatitis B Vaccines / therapeutic use*
  • Hepatitis B virus / genetics*
  • Hepatitis B virus / immunology*
  • Humans
  • Immunity, Mucosal / immunology
  • Injections, Intradermal / adverse effects
  • Middle Aged
  • Vaccines, DNA / adverse effects
  • Vaccines, DNA / therapeutic use*

Substances

  • Antibodies, Viral
  • DNA, Viral
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines
  • Vaccines, DNA