Comparison of the safety and immunogenicity of ACAM1000, ACAM2000 and Dryvax in healthy vaccinia-naive adults

Vaccine. 2009 Mar 4;27(10):1637-44. doi: 10.1016/j.vaccine.2008.11.079. Epub 2008 Dec 9.

Abstract

Currently, more than half of the world's population has no immunity against smallpox variola major virus. This phase I double-blind, randomized trial was conducted to compare the safety and immunogenicity of two clonally derived, cell-culture manufactured vaccinia strains, ACAM1000 and ACAM2000, to the parent vaccine, Dryvax. Thirty vaccinia-naïve subjects were enrolled into each of three groups and vaccines were administered percutaneously using a bifurcated needle at a dose of 1.0x10(8)PFU/mL. All subjects had a primary skin reaction indicating a successful vaccination. The adverse events, 4-fold neutralizing antibody rise and T cell immune responses were similar between the groups.

Publication types

  • Clinical Trial, Phase I
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Administration, Cutaneous
  • Adolescent
  • Adult
  • Antibodies, Viral / blood
  • Double-Blind Method
  • Female
  • Humans
  • Immunologic Memory
  • Male
  • Neutralization Tests
  • Safety
  • Skin / pathology
  • Skin / virology
  • Smallpox Vaccine / administration & dosage
  • Smallpox Vaccine / adverse effects
  • Smallpox Vaccine / immunology*
  • Smallpox Vaccine / pharmacology*
  • T-Lymphocytes / immunology
  • Vaccinia virus / immunology*
  • Vaccinia virus / isolation & purification
  • Young Adult

Substances

  • Antibodies, Viral
  • DryVax vaccine
  • Smallpox Vaccine