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The BCG replacement vaccine VPM1002: From drawing board to clinical trial

  • Stefan H.E. Kaufmann
  • , Mark F. Cotton
  • , Bernd Eisele
  • , Martin Gengenbacher
  • , Leander Grode
  • , Anneke C. Hesseling
  • , Gerhard Walzl
  • Max Planck Institute for Infection Biology
  • Stellenbosch University
  • Vakzine Projekt Management GmbH

Research output: Contribution to journal › Review article › peer-review

69 Scopus citations

Abstract

Tuberculosis remains a major health threat and vaccines better than bacillus Calmette-Guérin (BCG) are urgently required. Here we describe our experience with a recombinant BCG expressing listeriolysin and deficient in urease. This potential replacement vaccine has demonstrated superior efficacy and safety over BCG in Mycobacterium tuberculosis aerosol-challenged mice and was safe in numerous animal models including immune-deficient mice, guinea pigs, rabbits and nonhuman primates. Phase I clinical trials in adults in Germany and South Africa have proven safety and a current Phase IIa trial is under way to assess immunogenicity and safety in its target population, newborns in a high tuberculosis incidence setting, with promising early results. Second-generation candidates are being developed to improve safety and efficacy.

Original languageEnglish
Pages (from-to)619-630
Number of pages12
JournalExpert Review of Vaccines
Volume13
Issue number5
DOIs
StatePublished - May 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Mycobacterium tuberculosis
  • VPM1002
  • bacille Calmette'Gué rin
  • listeriolysin O
  • pre-exposure
  • prevention
  • prime vaccination
  • replacement
  • vaccine

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