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采用纯化初级液体标准品测定细胞季节性四价流感疫苗的效价。

Determination of the potency of a cell-based seasonal quadrivalent influenza vaccine using a purified primary liquid standard.

机构信息

Influenza Virus Research Center, National Institute of Infectious Diseases (NIID), Tokyo, Japan.

The Research Foundation for Microbial Diseases of Osaka University (BIKEN), Kagawa, Japan.

出版信息

Biologicals. 2020 Nov;68:32-39. doi: 10.1016/j.biologicals.2020.09.001. Epub 2020 Oct 3.

Abstract

In Japan, the practical application of completely cell-based seasonal influenza vaccines is under consideration. Considering the good correlation between the immunogenicity of egg-based influenza vaccines and the hemagglutinin (HA) content determined by the single radial immunodiffusion (SRD) assay, we determined the potency of the first cell-based quadrivalent vaccine experimentally generated in Japan using the SRD assay in this study. A primary liquid standard (PLS) and reference antigen were generated from the purified vaccine virus, and a sheep antiserum was produced against the HA of the vaccine virus. Since the purity of the PLS affects the reliability of vaccine potency testing, the purification steps are significant. We successfully prepared a purified PLS nearly free of cell debris. The HA content in the PLS was first estimated from the total amount of viral protein and the percentage of HA content determined by SDS-PAGE analysis. The HA content in the reference antigen was calibrated to that in the PLS via the SRD assay. The vaccine potency, that is, the HA content in each vaccine, was finally measured using the corresponding reference antigen. Ultimately, the measured vaccine potency of the monovalent vaccine was similar to that of the quadrivalent vaccine.

摘要

在日本,正在考虑将完全基于细胞的季节性流感疫苗实际应用。鉴于基于鸡蛋的流感疫苗的免疫原性与单扩散免疫沉淀(SRD)测定法确定的血凝素(HA)含量之间存在良好的相关性,本研究中我们使用 SRD 测定法来确定在日本首次实验生成的基于细胞的四价疫苗的效力。从纯化的疫苗病毒中生成主要液体标准品(PLS)和参考抗原,并针对疫苗病毒的 HA 产生绵羊抗血清。由于 PLS 的纯度会影响疫苗效力测试的可靠性,因此净化步骤非常重要。我们成功地制备了一种几乎不含细胞碎片的纯化 PLS。首先根据病毒蛋白总量和 SDS-PAGE 分析确定的 HA 含量百分比来估算 PLS 中的 HA 含量。通过 SRD 测定法对参考抗原中的 HA 含量进行校准。然后使用相应的参考抗原来测量疫苗效力,即每个疫苗中的 HA 含量。最终,单价疫苗的测量疫苗效力与四价疫苗的效力相似。

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