Department of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan.
Department of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan.
Vaccine. 2018 Oct 15;36(43):6449-6455. doi: 10.1016/j.vaccine.2018.09.021. Epub 2018 Sep 20.
Influenza becomes epidemic worldwide every year, and many individuals receive vaccination annually. Quality control relating to safety and potency of influenza vaccines is important to maintain public confidence. The safety of influenza vaccines has been assessed by clinical trials, and animal safety tests are performed to monitor the consistent quality between vaccines used for clinical trials and marketing; the biological responses in vaccinated animals are evaluated, including changes in body weight and white blood cell count. Animal safety tests have been contributing to the quality relating to the safety of influenza vaccines for decades, but improvements are needed. Although precise mechanisms involving biological changes in animal safety tests have not been fully elucidated, the application of cDNA microarray technology make it possible to reliably identify genes related to biological responses in vaccinated animals. From analysis of the expression profile of >10,000 genes of lung in animals treated with an inactivated whole virion influenza vaccine, we identified 17 marker genes whose expression patterns correlated well to changes in body weight and leukocyte count in vaccinated animals. In influenza HA vaccine-treated animals exhibiting subtle changes in biological responses, a robust expression pattern of marker genes was found. Furthermore, these marker genes could also be used in the evaluation of adjuvanted influenza vaccines. The expression profile of marker genes is expected to be an alternative indicator for safety control of various influenza vaccines conferring high sensitivity and short turnaround time. Thus, gene expression profiling may be a powerful tool for safety control of vaccines in the future.
流感每年在全球流行,许多人每年都接种疫苗。为了保持公众的信心,与流感疫苗的安全性和效力相关的质量控制非常重要。流感疫苗的安全性已通过临床试验进行评估,并且进行动物安全性测试以监测用于临床试验和上市的疫苗之间的一致性质量;评估接种动物的生物反应,包括体重和白细胞计数的变化。几十年来,动物安全性测试一直在为流感疫苗的安全性质量做出贡献,但仍需要改进。尽管尚未完全阐明动物安全性测试中涉及生物学变化的精确机制,但 cDNA 微阵列技术的应用使得可靠地识别与接种动物的生物学反应相关的基因成为可能。通过对用灭活全病毒流感疫苗处理的动物的肺部 >10000 个基因的表达谱进行分析,我们鉴定了 17 个标记基因,其表达模式与接种动物的体重和白细胞计数的变化密切相关。在表现出生物学反应细微变化的流感 HA 疫苗处理的动物中,发现了标记基因的强表达模式。此外,这些标记基因也可用于评估佐剂流感疫苗。预计标记基因的表达谱将成为具有高灵敏度和短周转时间的各种流感疫苗安全性控制的替代指标。因此,基因表达谱分析可能是未来疫苗安全性控制的有力工具。