Tanner Rachel, White Andrew D, Boot Charelle, Sombroek Claudia C, O'Shea Matthew K, Wright Daniel, Hoogkamer Emily, Bitencourt Julia, Harris Stephanie A, Sarfas Charlotte, Wittenberg Rachel, Satti Iman, Fletcher Helen A, Verreck Frank A W, Sharpe Sally A, McShane Helen
The Jenner Institute, University of Oxford, Oxford, UK.
Public Health England, Salisbury, UK.
NPJ Vaccines. 2021 Jan 4;6(1):3. doi: 10.1038/s41541-020-00263-7.
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.
我们展示了一种非人类灵长类动物分枝杆菌生长抑制试验(MGIA),该试验采用体外血液或细胞共培养,目的是优化和加速早期结核病疫苗测试。我们已采取措施,使用冷冻保存的外周血单核细胞优化该试验,将其转移至最终用户机构,并评估技术和生物学有效性。与旋转管相比,在静态48孔板中增加细胞浓度或分枝杆菌接种量并进行共培养,提高了试验内的重复性和灵敏度。标准化和协调工作产生了高度一致的结果,重复性和中间精密度的变异系数(CV)<10%,不同地点间的重现性CV<20%;尽管观察到了一些系统差异。作为概念验证,我们证明了能够在猕猴样本中检测到卡介苗疫苗诱导的生长抑制改善,并且在群体和个体动物水平上,MGIA结果与皮内接种卡介苗或气溶胶/支气管内接种结核分枝杆菌(M.tb)攻击后体内疾病发展的保护措施之间存在相关性。