Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
J Infect Dis. 2011 Jan 1;203(1):95-102. doi: 10.1093/infdis/jiq017.
The threat of a smallpox-based bioterrorist event or a human monkeypox outbreak has heightened the importance of new, safe vaccine approaches for these pathogens to complement older poxviral vaccine platforms. As poxviruses are large, complex viruses, they present technological challenges for simple recombinant vaccine development where a multicomponent mixtures of vaccine antigens are likely important in protection. We report that a synthetic, multivalent, highly concentrated, DNA vaccine delivered by a minimally invasive, novel skin electroporation microarray can drive polyvalent immunity in macaques, and offers protection from a highly pathogenic monkeypox challenge. Such a diverse, high-titer antibody response produced against 8 different DNA-encoded antigens delivered simultaneously in microvolumes has not been previously described. These studies represent a significant improvement in the efficiency of the DNA vaccine platform, resulting in immune responses that mimic live viral infections, and would likely have relevance for vaccine design against complex human and animal pathogens.
天花基生物恐怖事件或人类猴痘爆发的威胁,凸显了开发新的、安全的疫苗方法来对抗这些病原体的重要性,以补充旧的痘病毒疫苗平台。由于痘病毒是大型、复杂的病毒,因此对于简单的重组疫苗开发来说,它们存在技术挑战,因为多组分疫苗抗原混合物可能在保护中很重要。我们报告称,一种通过微创新型皮肤电穿孔微阵列递送的合成、多价、高浓度 DNA 疫苗可以在猕猴中引发多价免疫,并提供针对高致病性猴痘挑战的保护。这种针对 8 种不同 DNA 编码抗原的多样化、高滴度抗体反应,以微体积同时递送,以前尚未描述过。这些研究代表了 DNA 疫苗平台效率的显著提高,产生了模拟活病毒感染的免疫反应,并且可能与针对复杂的人类和动物病原体的疫苗设计相关。