A non-human primate in vitro functional assay for the early evaluation of TB vaccine candidates.
Rachel TannerAndrew D WhiteCharelle BootClaudia C SombroekMatthew K O'SheaDaniel WrightEmily HoogkamerJulia BitencourtStephanie A HarrisCharlotte SarfasRachel E WittenbergIman SattiHelen A FletcherFrank A W VerreckSally A SharpeHelen McShanePublished in: NPJ vaccines (2021)
We present a non-human primate mycobacterial growth inhibition assay (MGIA) using in vitro blood or cell co-culture with the aim of refining and expediting early tuberculosis vaccine testing. We have taken steps to optimise the assay using cryopreserved peripheral blood mononuclear cells, transfer it to end-user institutes, and assess technical and biological validity. Increasing cell concentration or mycobacterial input and co-culturing in static 48-well plates compared with rotating tubes improved intra-assay repeatability and sensitivity. Standardisation and harmonisation efforts resulted in high consistency agreements, with repeatability and intermediate precision <10% coefficient of variation (CV) and inter-site reproducibility <20% CV; although some systematic differences were observed. As proof-of-concept, we demonstrated ability to detect a BCG vaccine-induced improvement in growth inhibition in macaque samples, and a correlation between MGIA outcome and measures of protection from in vivo disease development following challenge with either intradermal BCG or aerosol/endobronchial Mycobacterium tuberculosis (M.tb) at a group and individual animal level.
Keyphrases
- mycobacterium tuberculosis
- high throughput
- endothelial cells
- pulmonary tuberculosis
- single cell
- high glucose
- induced pluripotent stem cells
- cell therapy
- magnetic resonance imaging
- emergency department
- stem cells
- quality improvement
- mesenchymal stem cells
- computed tomography
- hiv aids
- magnetic resonance
- drug induced
- bone marrow
- antiretroviral therapy
- umbilical cord
- human immunodeficiency virus
- water soluble