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利用基因表达谱建立流感疫苗和佐剂的新质量控制及疫苗安全性检测方法。

Establishment of a new quality control and vaccine safety test for influenza vaccines and adjuvants using gene expression profiling.

作者信息

Momose Haruka, Mizukami Takuo, Kuramitsu Madoka, Takizawa Kazuya, Masumi Atsuko, Araki Kumiko, Furuhata Keiko, Yamaguchi Kazunari, Hamaguchi Isao

机构信息

Department of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.

出版信息

PLoS One. 2015 Apr 24;10(4):e0124392. doi: 10.1371/journal.pone.0124392. eCollection 2015.

DOI:10.1371/journal.pone.0124392
PMID:25909814
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4409070/
Abstract

We have previously identified 17 biomarker genes which were upregulated by whole virion influenza vaccines, and reported that gene expression profiles of these biomarker genes had a good correlation with conventional animal safety tests checking body weight and leukocyte counts. In this study, we have shown that conventional animal tests showed varied and no dose-dependent results in serially diluted bulk materials of influenza HA vaccines. In contrast, dose dependency was clearly shown in the expression profiles of biomarker genes, demonstrating higher sensitivity of gene expression analysis than the current animal safety tests of influenza vaccines. The introduction of branched DNA based-concurrent expression analysis could simplify the complexity of multiple gene expression approach, and could shorten the test period from 7 days to 3 days. Furthermore, upregulation of 10 genes, Zbp1, Mx2, Irf7, Lgals9, Ifi47, Tapbp, Timp1, Trafd1, Psmb9, and Tap2, was seen upon virosomal-adjuvanted vaccine treatment, indicating that these biomarkers could be useful for the safety control of virosomal-adjuvanted vaccines. In summary, profiling biomarker gene expression could be a useful, rapid, and highly sensitive method of animal safety testing compared with conventional methods, and could be used to evaluate the safety of various types of influenza vaccines, including adjuvanted vaccine.

摘要

我们之前已鉴定出17个被全病毒流感疫苗上调的生物标志物基因,并报告这些生物标志物基因的基因表达谱与检查体重和白细胞计数的传统动物安全性试验具有良好的相关性。在本研究中,我们发现传统动物试验在流感HA疫苗系列稀释的散装材料中显示出不同且无剂量依赖性的结果。相比之下,生物标志物基因的表达谱中明显呈现出剂量依赖性,这表明基因表达分析比当前流感疫苗的动物安全性试验具有更高的灵敏度。引入基于分支DNA的同时表达分析可以简化多基因表达方法的复杂性,并可将测试周期从7天缩短至3天。此外,在使用病毒体佐剂疫苗处理后,观察到10个基因Zbp1、Mx2、Irf7、Lgals9、Ifi47、Tapbp、Timp1、Trafd1、Psmb9和Tap2上调,这表明这些生物标志物可用于病毒体佐剂疫苗的安全性控制。总之,与传统方法相比,分析生物标志物基因表达可能是一种有用、快速且高度灵敏的动物安全性测试方法,可用于评估包括佐剂疫苗在内的各种类型流感疫苗的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed54/4409070/aa2245bc088e/pone.0124392.g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed54/4409070/16d7690f50e7/pone.0124392.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed54/4409070/91734fa26ad4/pone.0124392.g004.jpg
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