Scientific and Research Institute for Medical and Veterinary Biotechnologies, Russia-Switzerland, Branch in Saratov, 9 Proviantskaya Street, Box 1580, Saratov 410028, Russia.
Expert Rev Vaccines. 2009 Dec;8(12):1721-38. doi: 10.1586/erv.09.129.
The potential application of Yersinia pestis for bioterrorism emphasizes the urgent need to develop more effective vaccines against airborne infection. The current status of plague vaccines has been reviewed. The present emphasis is on subunit vaccines based on the F1 and LcrV antigens. These provide good protection in animal models but may not protect against F1 strains with modifications to the type III secretion system. The duration of protection against pneumonic infection is also uncertain. Other strategies under investigation include defined live-attenuated vaccines, DNA vaccines, mucosal delivery systems and heterologous immunization. The live-attenuated strain Y. pestis EV NIIEG protects against aerosol challenge in animal models and, with further modification to reduce residual virulence and to optimize respiratory protection, it could provide a shortcut to improved vaccines. The regulatory problems inherent in licensing vaccines for which efficacy data are unavailable and their possible solutions are discussed herein.
鼠疫耶尔森菌用于生物恐怖主义的潜在应用强调了迫切需要开发更有效的针对空气传播感染的疫苗。本文回顾了鼠疫疫苗的现状。目前的重点是基于 F1 和 LcrV 抗原的亚单位疫苗。这些疫苗在动物模型中提供了良好的保护,但可能不能预防 III 型分泌系统发生修饰的 F1 菌株。针对肺鼠疫感染的保护持续时间也不确定。其他正在研究的策略包括明确的减毒活疫苗、DNA 疫苗、黏膜传递系统和异源免疫接种。减毒活菌株 Y. pestis EV NIIEG 可在动物模型中预防气溶胶攻击,并且通过进一步修饰以降低残余毒力并优化呼吸道保护,它可以为改进疫苗提供捷径。本文讨论了在没有功效数据的情况下许可疫苗的固有监管问题及其可能的解决方案。