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首页> 外文期刊>Journal of Virological Methods >Development of a sandwich ELISA to detect virus-like-particles in enterovirus A71 vaccines
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Development of a sandwich ELISA to detect virus-like-particles in enterovirus A71 vaccines

机译:夹心ELISA的开发,以检测肠道病毒A71疫苗的病毒样颗粒

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The goal of this paper was to develop a sandwich ELISA that can detect intact human enterovirus A71 (EV-A71) virus-like particles (VLPs) in vaccines. This assay specifically detected EV-A71 viruses from different sub-genogroups as well as EV-A71 VLPs, and treatment of VLPs with high heat and low pH reduced or completely abolished detection of the VLPs suggesting that the ELISA detected assembled particles. Using a purified VLP as a reference standard, a quantitative sandwich ELISA (Q-ELISA) was established which was used to monitor the yield and purity of the VLPs during manufacturing. Coupled with immunogenicity studies, the Q-ELISA was used to evaluate the performance of the VLPs and formalin-inactivated EV-A71 vaccine. This assay has the potential to play an important role in the development of an efficient process to produce and purify the VLPs and in examining the quality of EV-A71 vaccines.
机译:本文的目标是开发一个夹心ELISA,可以在疫苗中检测完整的人肠道病毒A71(EV-A71)病毒样颗粒(VLP)。 该测定特异性地检测来自不同亚基因组的EV-A71病毒以及EV-A71 VLP,并且具有高热量和低pH的VLP,降低或完全消除了VLP的检测,表明ELISA检测到的组装颗粒。 使用纯化的VLP作为参考标准,建立了定量夹心ELISA(Q-ELISA),其用于监测制造过程中VLP的产量和纯度。 结合免疫原性研究,Q-ELISA用于评估VLP和福尔马林 - 失活的EV-A71疫苗的性能。 该测定有可能在开发有效的过程中发挥重要作用,以生产和纯化VLP和检查EV-A71疫苗的质量。

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