Jacobs Bertram L, Langland Jeffrey O, Kibler Karen V, Denzler Karen L, White Stacy D, Holechek Susan A, Wong Shukmei, Huynh Trung, Baskin Carole R
School of Life Sciences, Arizona State University, Tempe, AZ 85287-5401, USA.
Antiviral Res. 2009 Oct;84(1):1-13. doi: 10.1016/j.antiviral.2009.06.006. Epub 2009 Jun 26.
Vaccinia virus (VACV) has been used more extensively for human immunization than any other vaccine. For almost two centuries, VACV was employed to provide cross-protection against variola virus, the causative agent of smallpox, until the disease was eradicated in the late 1970s. Since that time, continued research on VACV has produced a number of modified vaccines with improved safety profiles. Attenuation has been achieved through several strategies, including sequential passage in an alternative host, deletion of specific genes or genetic engineering of viral genes encoding immunomodulatory proteins. Some highly attenuated third- and fourth-generation VACV vaccines are now being considered for stockpiling against a possible re-introduction of smallpox through bioterrorism. Researchers have also taken advantage of the ability of the VACV genome to accommodate additional genetic material to produce novel vaccines against a wide variety of infectious agents, including a recombinant VACV encoding the rabies virus glycoprotein that is administered orally to wild animals. This review provides an in-depth examination of these successive generations of VACV vaccines, focusing on how the understanding of poxviral replication and viral gene function permits the deliberate modification of VACV immunogenicity and virulence.
痘苗病毒(VACV)用于人类免疫的范围比其他任何疫苗都更为广泛。在近两个世纪的时间里,痘苗病毒一直被用于提供针对天花致病因子天花病毒的交叉保护,直到20世纪70年代末天花病被根除。从那时起,对痘苗病毒的持续研究产生了一些安全性更高的改良疫苗。通过多种策略实现了减毒,包括在替代宿主中连续传代、删除特定基因或对编码免疫调节蛋白的病毒基因进行基因工程改造。目前正在考虑储备一些高度减毒的第三代和第四代痘苗病毒疫苗,以防天花通过生物恐怖主义再次出现。研究人员还利用痘苗病毒基因组容纳额外遗传物质的能力,生产针对多种传染病原体的新型疫苗,包括一种编码狂犬病病毒糖蛋白的重组痘苗病毒,可口服给野生动物。这篇综述对这些历代痘苗病毒疫苗进行了深入研究,重点关注对痘病毒复制和病毒基因功能的理解如何能够有意地改变痘苗病毒的免疫原性和毒力。