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Evaluation of marker gene expression as a potential predictive marker of leukopenic toxicity for inactivated influenza vaccines

机译:标志物基因表达作为灭活流感疫苗白盲毒性潜在预测标志物的评价

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Abstract The leukopenic toxicity test (LTT) is used to evaluate the safety and lot-to-lot consistency of influenza hemagglutinin split vaccine (HAv) and is included in the Japanese Minimum Requirements for Biological Products. LTT assesses the reduced leukocyte levels in murine peripheral blood after HAv administration. However, they require large numbers of animals, and therefore it would be beneficial to develop a more accurate and sensitive alternative method. In this study, we selected biomarkers of leukocyte reduction from 18 previously identified marker genes that were associated with an abnormal toxicity test (ATT). Among these 18 genes, the expressions of 15 marker genes were strongly associated with leukocyte reduction levels. A stepwise single addition multiple regression analysis was used to further extract the genes responsible for leukocyte reduction, with significant ( p ? 90% (mean) for the direct measurement of leukocyte numbers. These results indicate that the expression of these 18 previously identified genes can provide information for both ATT and LTT.
机译:摘要使用白细胞毒性测试(LTT)来评估流感血凝素分裂疫苗(HAV)的安全性和批量达到浓度,并包含在日本的生物产品的最低要求中。 LTT评估HAV给药后鼠外周血中的降低的白细胞水平。然而,它们需要大量的动物,因此开发更准确和灵敏的替代方法是有益的。在这项研究中,我们选择了从先前鉴定的标记基因的白细胞减少的生物标志物,该标记基因与异常毒性试验(ATT)相关。在这18个基因中,15个标记基因的表达与白细胞减少水平强烈相关。逐步单一添加多元回归分析用于进一步提取负责白细胞减少的基因,显着(p≤90%(平均值),用于直接测量白细胞数。这些结果表明这18个先前鉴定的基因的表达可以提供ATT和LTT的信息。

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