Charo Jehad, Lindencrona Jan Alvar, Carlson Lena-Maria, Hinkula Jorma, Kiessling Rolf
Department of Oncology-Pathology, Cancer Center Karolinska (CCK), Karolinska Hospital, R8:01, S-171 76 Stockholm, Sweden.
J Virol. 2004 Oct;78(20):11321-6. doi: 10.1128/JVI.78.20.11321-11326.2004.
Effective vaccination against heterologous influenza virus infection remains elusive. Immunization with plasmid DNA (pDNA) expressing conserved genes from influenza virus is a promising approach to achieve cross-variant protection. However, despite having been described for more than a decade, pDNA vaccination still requires further optimization to be applied clinically as a standard vaccination approach. We have recently described a simple and efficient approach to enhance pDNA immunization, based on the use of tucaresol, a Schiff base-forming drug. In this report we have tested the ability of this drug to increase the protection conferred by pDNA vaccination against influenza virus infection. Our results demonstrate that a significant protection was achieved in two strains of mice by using the combination of pDNA and tucaresol. This protection was associated with an elevated humoral and cellular response and a switch in the type of the T helper cell (Th) immune response from type 2 to type 1. This vaccine combination represents a promising strategy for designing a clinical study for the protection from influenza and similar infections.
有效预防异源流感病毒感染的疫苗接种仍然难以实现。用表达流感病毒保守基因的质粒DNA(pDNA)进行免疫是实现交叉变异保护的一种有前景的方法。然而,尽管pDNA疫苗接种已被描述了十多年,但仍需要进一步优化才能作为标准疫苗接种方法应用于临床。我们最近描述了一种基于使用席夫碱形成药物图卡雷索尔的简单有效的增强pDNA免疫的方法。在本报告中,我们测试了这种药物增强pDNA疫苗接种对流感病毒感染保护作用的能力。我们的结果表明,通过使用pDNA和图卡雷索尔的组合,在两种小鼠品系中都实现了显著的保护作用。这种保护与体液和细胞反应的增强以及T辅助细胞(Th)免疫反应类型从2型向1型的转变有关。这种疫苗组合代表了一种有前景的策略,可用于设计预防流感和类似感染的临床研究。