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口蹄疫疫苗抗原过程定量预处理方法的验证

Validation of Pretreatment Methods for the In-Process Quantification of Foot-and-Mouth Disease Vaccine Antigens.

作者信息

Kim Ah-Young, Park Sun Young, Park Sang Hyun, Jin Jong Sook, Kim Eun-Sol, Kim Jae Young, Park Jong-Hyeon, Ko Young-Joon

机构信息

Center for FMD Vaccine Research, Animal and Plant Quarantine Agency, Gimcheon 39660, Korea.

出版信息

Vaccines (Basel). 2021 Nov 19;9(11):1361. doi: 10.3390/vaccines9111361.

Abstract

Foot-and-mouth disease (FMD), caused by the FMD virus (FMDV), is controlled by vaccine policy in many countries. For vaccine potency, the content of intact virus particles (146S antigens) is critical, and the sucrose density gradient (SDG) fractionation is the gold standard for the quantification of 146S antigens. However, this method has several drawbacks. Although size-exclusion high-performance liquid chromatography (SE-HPLC) was introduced to replace the classic method, its application is generally confined to purified samples owing to the interfering signals. Therefore, we aimed to develop optimal pretreatment methods for SE-HPLC quantification in less purified samples. Crude virus infection supernatant (CVIS) and semi-purified samples with PEG precipitation (PEG-P) were used. Chloroform pretreatment was essential to remove a high level of non-specific signals in CVIS, whereas it caused loss of 146S antigens without the distinctive removal of non-specific signals in PEG-P. Benzonase pretreatment was required to improve the resolution of the target peak in the chromatogram for both CVIS and PEG-P. Through spiking tests with pure 146S antigens, it was verified that the combined pretreatment with chloroform and benzonase was optimal for the CVIS, while the sole pretreatment of benzonase was beneficial for PEG-P.

摘要

口蹄疫(FMD)由口蹄疫病毒(FMDV)引起,在许多国家通过疫苗政策进行控制。对于疫苗效力而言,完整病毒颗粒(146S抗原)的含量至关重要,蔗糖密度梯度(SDG)分级分离是定量146S抗原的金标准。然而,该方法存在若干缺点。尽管引入了尺寸排阻高效液相色谱法(SE-HPLC)来取代经典方法,但由于干扰信号,其应用通常仅限于纯化样品。因此,我们旨在开发用于在纯化程度较低的样品中进行SE-HPLC定量的最佳预处理方法。使用粗病毒感染上清液(CVIS)和经聚乙二醇沉淀的半纯化样品(PEG-P)。氯仿预处理对于去除CVIS中的高水平非特异性信号至关重要,而在PEG-P中它会导致146S抗原损失且无法有效去除非特异性信号。对于CVIS和PEG-P,都需要用核酸酶进行预处理以提高色谱图中目标峰的分辨率。通过用纯146S抗原进行加标试验,证实氯仿和核酸酶联合预处理对CVIS是最佳的,而单独使用核酸酶预处理对PEG-P有益。

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