Kofler Regina M, Aberle Judith H, Aberle Stephan W, Allison Steven L, Heinz Franz X, Mandl Christian W
Institute of Virology, Medical University of Vienna, Kinderspitalgasse 15, A-1095 Vienna, Austria.
Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1951-6. doi: 10.1073/pnas.0307145101. Epub 2004 Feb 9.
Flaviviruses are human pathogens of world-wide medical importance. They have recently received much additional attention because of their spread to new regions (such as West Nile virus to North America), highlighting their potential as newly emerging disease agents. Using tick-borne encephalitis virus, we have developed and evaluated in mice a new genetic vaccine based on self-replicating but noninfectious RNA. This RNA contains all of the necessary genetic information for establishing its replication machinery in the host cell, thus mimicking a natural infection. However, genetic modifications in the region encoding the capsid protein simultaneously prevent the assembly of infectious virus particles and promote the secretion of noninfectious subviral particles that elicit neutralizing antibodies. These characteristics demonstrate that a new generation of flavivirus vaccines can be designed that stimulate the same spectrum of innate and specific immune responses as a live vaccine but have the safety features of an inactivated vaccine.
黄病毒是具有全球医学重要性的人类病原体。由于它们传播到新的地区(如西尼罗河病毒传播到北美),最近受到了更多关注,凸显了它们作为新兴致病原的潜力。我们利用蜱传脑炎病毒,在小鼠中开发并评估了一种基于自我复制但无感染性RNA的新型基因疫苗。这种RNA包含在宿主细胞中建立其复制机制所需的所有遗传信息,从而模拟自然感染。然而,衣壳蛋白编码区的基因修饰同时可防止感染性病毒颗粒的组装,并促进引发中和抗体的无感染性子病毒颗粒的分泌。这些特性表明,可以设计出新一代黄病毒疫苗,其能刺激与活疫苗相同的先天性和特异性免疫反应谱,但具有灭活疫苗的安全特性。