Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Vaccine. 2012 Feb 1;30(6):1038-49. doi: 10.1016/j.vaccine.2011.12.044. Epub 2011 Dec 18.
The varied rates of protection induced by Mycobacterium bovis BCG vaccine against tuberculosis has been attributed to many factors such as genetic variability among BCG strains, rapid clearance of BCG in some populations, and different levels of previous exposure of vaccinated populations to environmental mycobacteria. However, the methods and conditions employed to prepare this vaccine for human usage by various manufacturers have not been investigated as potential factors contributing to the variation in vaccine efficacy. A review of the literature indicates discrepancies between the approach for growing BCG vaccine in the laboratory to assess immune responses and protective ability in animal models, and that employed for production of the vaccine for administration to humans. One of the major differences is in the growth medium used for routine propagation in the laboratory and the one used for bulk vaccine production by manufacturers. Here we compared the immunogenicity of the BCG vaccine grown in Middlebrook 7H9 medium, the most commonly used medium in laboratory studies, against that grown in Sauton medium, which is used for growing BCG by most manufacturers. Our results showed clear differences in the behavior of BCG grown in these different culture media. Compared to BCG grown in Middlebrook 7H9 medium, BCG grown in Sauton media was more persistent inside macrophages, more effective at inhibiting apoptosis of infected cells, induced stronger inflammatory responses and stimulated less effective immunity against aerosol challenge with a virulent Mtb strain. These findings suggested that the growth medium used for producing BCG vaccine is an important factor that deserves increased scrutiny in ongoing efforts to produce more consistently effective vaccines against Mtb.
牛型结核分枝杆菌卡介苗(BCG)疫苗对结核病的保护率存在差异,其原因有很多,如 BCG 菌株的遗传变异性、某些人群中 BCG 的快速清除、以及接种人群对环境分枝杆菌的既往暴露程度不同等。然而,不同制造商用于制备人类 BCG 疫苗的方法和条件尚未被视为导致疫苗效力差异的潜在因素。文献综述表明,实验室中用于评估免疫反应和动物模型保护能力的 BCG 疫苗培养方法与用于向人类接种疫苗的生产方法之间存在差异。其中一个主要区别是在实验室中常规繁殖中使用的生长培养基与制造商用于批量生产疫苗的培养基之间的差异。在这里,我们比较了在最常用于实验室研究的 Middlebrook 7H9 培养基中生长的 BCG 疫苗与在大多数制造商用于生长 BCG 的 Sauton 培养基中生长的 BCG 的免疫原性。我们的结果表明,在这些不同的培养基中生长的 BCG 行为存在明显差异。与在 Middlebrook 7H9 培养基中生长的 BCG 相比,在 Sauton 培养基中生长的 BCG 在巨噬细胞内更持久,更有效地抑制感染细胞的凋亡,诱导更强的炎症反应,并刺激对有活力的 Mtb 菌株气溶胶挑战的免疫应答效果较差。这些发现表明,用于生产 BCG 疫苗的生长培养基是一个重要因素,值得在生产更一致有效的 Mtb 疫苗的持续努力中进一步研究。