Safety and immunogenicity of boosting BCG vaccinated subjects with BCG: comparison with boosting with a new TB vaccine, MVA85A

PLoS One. 2009 Jun 16;4(6):e5934. doi: 10.1371/journal.pone.0005934.

Abstract

Objectives: To investigate the safety and immunogenicity of a booster BCG vaccination delivered intradermally in healthy, BCG vaccinated subjects and to compare with a previous clinical trial where BCG vaccinated subjects were boosted with a new TB vaccine, MVA85A.

Design: Phase I open label observational trial, in the UK. Healthy, HIV-negative, BCG vaccinated adults were recruited and vaccinated with BCG. The primary outcome was safety; the secondary outcome was cellular immune responses to antigen 85, overlapping peptides of antigen 85A and tuberculin purified protein derivative (PPD) detected by ex vivo interferon-gamma (IFN-gamma) ELISpot assay and flow cytometry.

Results and conclusions: BCG revaccination (BCG-BCG) was well tolerated, and boosting of pre-existing PPD-specific T cell responses was observed. However, when these results were compared with data from a previous clinical trial, where BCG was boosted with MVA85A (BCG-MVA85A), MVA85A induced significantly higher levels (>2-fold) of antigen 85-specific CD4+ T cells (both antigen and peptide pool responses) than boosting with BCG, up to 52 weeks post-vaccination (p = 0.009). To identify antigen 85A-specific CD8+ T cells that were not detectable by ex vivo ELISpot and flow cytometry, dendritic cells (DC) were used to amplify CD8+ T cells from PBMC samples. We observed low, but detectable levels of antigen 85A-specific CD8+ T cells producing IFNgamma (1.5% of total CD8 population) in the BCG primed subjects after BCG boosting in 1 (20%) of 5 subjects. In contrast, in BCG-MVA85A vaccinated subjects, high levels of antigen 85A-specific CD8+ T cells (up to 14% total CD8 population) were observed after boosting with MVA85A, in 4 (50%) of 8 subjects evaluated. In conclusion, revaccination with BCG resulted in modest boosting of pre-existing immune responses to PPD and antigen 85, but vaccination with BCG-MVA85A induced a significantly higher response to antigen 85 and generated a higher frequency of antigen 85A-specific CD8+ T cells.

Trial registration: ClinicalTrials.gov NCT00654316 NCT00427830.

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases / chemistry
  • Acyltransferases / immunology*
  • Adult
  • Antigens, Bacterial / chemistry
  • Antigens, Bacterial / immunology*
  • BCG Vaccine / administration & dosage*
  • BCG Vaccine / chemistry
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / virology
  • Dendritic Cells / virology*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Flow Cytometry / methods
  • Humans
  • Interferon-gamma / metabolism
  • Male
  • Middle Aged
  • Peptides / chemistry
  • Time Factors
  • Tuberculosis Vaccines / chemistry*

Substances

  • Antigens, Bacterial
  • BCG Vaccine
  • Peptides
  • Tuberculosis Vaccines
  • Interferon-gamma
  • Acyltransferases
  • antigen 85A, Mycobacterium tuberculosis

Associated data

  • ClinicalTrials.gov/NCT00427830
  • ClinicalTrials.gov/NCT00654316