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PRODUCTION OF BACTERIAL OUTER MEMBRANE VESICLES AS VACCINE PLATFORM

机译:生产细菌外膜囊泡作为疫苗平台

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Bacterial outer membrane vesicles (OMVs) are non-infectious but highly immunogenic particles. These vesicles are used as vaccines against the disease of the source bacteria. Fascinatingly, the addition of heterologous antigens to these vesicles creates a versatile vaccine platform. Such a platform can be used as an alternative to subunit vaccines, during infectious disease outbreaks or for the development of vaccines against pathogens that require high containment. A unique aspect of this platform is the reusability of the production process for many different vaccines. This in turn could reduce the time to market for new vaccines significantly. We designed a heterologous OMV vaccine concept for Lyme disease based on spontaneous released OMVs from Neisseria meningitidis that express the Outer surface protein A (OspA) of Borrelia burgdorferi on the surface. The productivity of spontaneously released OMVs was improved by the introduction of oxidative stress to the bacterial culture. Increased dissolved oxygen concentrations during cultivation showed to be an excellent process parameter for enhanced release of OMVs, while the bacterial culture remains viable. This presentation will cover the development of the OMV-based vaccine platform and the impact of changes in the upstream process on the downstream process of the investigational OMV-based Lyme disease vaccine.
机译:细菌外膜囊泡(OMV)是非传染性但高度免疫原性颗粒。这些囊泡用作抗源细菌疾病的疫苗。迷人地,向这些囊泡中添加异源抗原产生通用的疫苗平台。这种平台可以用作亚基疫苗的替代物,在传染病爆发期间或用于对需要高容忍的病原体的疫苗的发育。该平台的一个独特方面是许多不同疫苗的生产过程的可重用性。这反过来可以减少对新疫苗的市场的时间显着。我们为基于自发释放的OMV的leme疾病设计了一种异源OMV疫苗概念,从脑膜炎脑炎症的外表蛋白A(OSPA)在表面上表达外表蛋白A(OSPA)。通过引入细菌培养的氧化胁迫改善了自发释放的OMV的生产率。培养过程中溶解氧浓度的增加显示是一种优异的方法参数,用于增强OMV的释放,而细菌培养物仍然可行。本演示文稿将涵盖基于OMV的疫苗平台的发展以及上游过程变化对研究基于OMV的血清疾病疫苗的下游过程的影响。

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