Development and application of the direct mycobacterial growth inhibition assay: a systematic review

Front Immunol. 2024 Feb 6:15:1355983. doi: 10.3389/fimmu.2024.1355983. eCollection 2024.

Abstract

Introduction: First described by Wallis et al. in 2001 for the assessment of TB drugs, the direct mycobacterial growth inhibition assay (MGIA) offers a tractable ex vivo tool measuring the combined influences of host immunity, strain virulence and intervention effects. Over the past 13 years, we have led efforts to adapt the direct MGIA for the assessment of TB vaccines including optimisation, harmonisation and validation of BCG vaccine-induced responses as a benchmark, as well as assay transfer to institutes worldwide.

Methods: We have performed a systematic review on the primary published literature describing the development and applications of the direct MGIA from 2001 to June 2023 in accordance with the PRISMA reporting guidelines.

Results: We describe 63 studies in which the direct MGIA has been applied across species for the evaluation of TB drugs and novel TB vaccine candidates, the study of clinical cohorts including those with comorbidities, and to further understanding of potential immune correlates of protection from TB. We provide a comprehensive update on progress of the assay since its conception and critically evaluate current findings and evidence supporting its utility, highlighting priorities for future directions.

Discussion: While further standardisation and validation work is required, significant advancements have been made in the past two decades. The direct MGIA provides a potentially valuable tool for the early evaluation of TB drug and vaccine candidates, clinical cohorts, and immune mechanisms of mycobacterial control.

Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42023423491.

Keywords: BCG; MGIA; mycobacterial growth inhibition assay; tuberculosis; vaccines.

Publication types

  • Systematic Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • BCG Vaccine
  • Humans
  • Mycobacterium tuberculosis*
  • Tuberculosis Vaccines
  • Tuberculosis* / microbiology

Substances

  • BCG Vaccine
  • Tuberculosis Vaccines