Institute of Virology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 05 Bratislava, Slovak Republic.
Arch Virol. 2012 May;157(5):811-7. doi: 10.1007/s00705-012-1238-6.
Although influenza DNA vaccine research has focused mainly on viral hemagglutinin and has led to promising results, other virion proteins have also shown some protective potential. In this work, we explored the potential of a DNA vaccine based on the PB1 protein to protect BALB/c mice against lethal influenza A virus infection. The DNA vaccine consisted of pTriEx4 plasmid expressing PB1. As a positive control, a pTriEx4 plasmid expressing influenza A virus HA was used. Two weeks after three subcutaneous doses of DNA vaccine, the mice were challenged intranasally with 1 LD50 of A/Puerto Rico/8/34 (H1N1) virus, and PB1- and HA-specific antibodies, survival rate, body weight change, viral mRNA load, infectious virus titer in the lungs, cytokines IL-2, IL-4 and IL-10, and granzyme-B were measured. The results showed that (i) the PB1-expressing DNA vaccine provided a fair protective immunity in the mouse model and (ii) viral structural proteins such as PB1 represent promising antigens for DNA vaccination against influenza A.
虽然流感 DNA 疫苗的研究主要集中在病毒血凝素上,并取得了有希望的结果,但其他病毒蛋白也显示出了一些保护潜力。在这项工作中,我们探索了基于 PB1 蛋白的 DNA 疫苗在保护 BALB/c 小鼠免受致死性流感病毒感染方面的潜力。该 DNA 疫苗由表达 PB1 的 pTriEx4 质粒组成。作为阳性对照,使用表达流感 A 病毒 HA 的 pTriEx4 质粒。在三次皮下接种 DNA 疫苗两周后,小鼠经鼻腔内感染 1 LD50 的 A/Puerto Rico/8/34(H1N1)病毒,并测量 PB1 和 HA 特异性抗体、存活率、体重变化、病毒 mRNA 载量、肺内感染性病毒滴度、细胞因子 IL-2、IL-4 和 IL-10 以及颗粒酶-B。结果表明:(i)表达 PB1 的 DNA 疫苗在小鼠模型中提供了良好的保护免疫;(ii)病毒结构蛋白如 PB1 代表了针对流感 A 的 DNA 疫苗接种的有希望的抗原。