Recombinant tuberculosis vaccine AEC/BC02 induces antigen-specific cellular responses in mice and protects guinea pigs in a model of latent infection

J Microbiol Immunol Infect. 2015 Dec;48(6):597-603. doi: 10.1016/j.jmii.2014.03.005. Epub 2014 May 23.

Abstract

Purpose: To preliminarily evaluate the immunogenicity and efficacy of the recombinant tuberculosis vaccine AEC/BC02 in which Ag85b and fusion protein ESAT6-CFP10 were combined with bacillus Calmette-Guérin CpG and an aluminum salt-based adjuvant system.

Methods: Groups of BALB/c mice were immunized intramuscularly three times at 10-day intervals with AEC/BC02 or the adjuvant alone and the vaccine-induced cell-mediated immune responses were evaluated. The efficacy of AEC/BC02 was evaluated in two guinea pig models, one a model of prevention and the other a model of latent infection.

Results: The AEC/BC02 vaccine induced strong cellular immune responses characterized by a high frequency of antigen-specific interferon-γ-secreting T cells in mice at different time points after the last vaccination. In the preventive model of guinea pig, AEC/BC02 did not protect against Mycobacterium tuberculosis as a pre-exposure vaccine. However, in a latent infection model of guinea pig, it effectively controlled the reactivation of M. tuberculosis and lowered the bacterial load in the lung and spleen.

Conclusion: These results indicate AEC/BC02 can protect against reactivation of latent infection and may function as a therapeutic vaccine.

Keywords: CpG adjuvant; Mycobacterium tuberculosis; guinea pig; latent tuberculosis infection; recombinant vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bacterial / immunology
  • Antigens, Bacterial / immunology*
  • BCG Vaccine / immunology
  • Bacterial Load / immunology
  • Disease Models, Animal
  • Guinea Pigs
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Latent Tuberculosis / immunology*
  • Latent Tuberculosis / microbiology
  • Latent Tuberculosis / prevention & control
  • Lung / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Mycobacterium tuberculosis / immunology*
  • Spleen / microbiology
  • Th1 Cells / immunology*
  • Tuberculosis Vaccines / immunology*
  • Vaccination
  • Vaccines, Synthetic / immunology*

Substances

  • Antibodies, Bacterial
  • Antigens, Bacterial
  • BCG Vaccine
  • Tuberculosis Vaccines
  • Vaccines, Synthetic
  • Interferon-gamma