Sun Wei, Roland Kenneth L, Curtiss Roy
Center for Infectious Disease and Vaccinology, The Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, AZ 85287-5401 , USA.
J Infect Dev Ctries. 2011 Sep 14;5(9):614-27. doi: 10.3855/jidc.2030.
Three great plague pandemics caused by the gram-negative bacterium Yersinia pestis have killed nearly 200 million people and it has been linked to biowarfare in the past. Plague is endemic in many parts of the world. In addition, the risk of plague as a bioweapon has prompted increased research to develop plague vaccines against this disease. Injectable subunit vaccines are being developed in the United States and United Kingdom. However, the live attenuated Y. pestis-EV NIIEG strain has been used as a vaccine for more than 70 years in the former Soviet Union and in some parts of Asia and provides a high degree of efficacy against plague. This vaccine has not gained general acceptance because of safety concerns. In recent years, modern molecular biological techniques have been applied to Y. pestis to construct strains with specific defined mutations designed to create safe, immunogenic vaccines with potential for use in humans and as bait vaccines to reduce the load of Y. pestis in the environment. In addition, a number of live, vectored vaccines have been reported using attenuated viral vectors or attenuated Salmonella strains to deliver plague antigens. Here we summarize the progress of live attenuated vaccines against plagu.
由革兰氏阴性细菌鼠疫耶尔森菌引发的三次重大鼠疫大流行已导致近2亿人死亡,并且在过去它曾与生物战有关联。鼠疫在世界许多地区呈地方性流行。此外,鼠疫作为生物武器的风险促使人们加大了研发针对该疾病的鼠疫疫苗的研究力度。美国和英国正在研发可注射亚单位疫苗。然而,减毒活鼠疫耶尔森菌-EV NIIEG菌株在前苏联以及亚洲部分地区作为疫苗已使用了70多年,并且对鼠疫具有高度疗效。由于安全问题,这种疫苗尚未获得广泛认可。近年来,现代分子生物学技术已应用于鼠疫耶尔森菌,以构建具有特定明确突变的菌株,旨在制造出安全、具有免疫原性且有可能用于人类的疫苗以及作为诱饵疫苗以减少环境中鼠疫耶尔森菌的数量。此外,已经报道了一些使用减毒病毒载体或减毒沙门氏菌菌株来递送鼠疫抗原的活载体疫苗。在此,我们总结了抗鼠疫减毒活疫苗的进展。