Bowick Gavin C, McAuley Alexander J
Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Bioeng Bugs. 2011 May-Jun;2(3):129-35. doi: 10.4161/bbug.2.3.15367. Epub 2011 May 1.
Vaccination is currently the most effective strategy to medically control viral diseases. However, developing vaccines is a long and expensive process, and traditional methods, such as attenuating wild-type viruses by serial passage, may not be suitable for all viruses and may lead to vaccine safety considerations, particularly in the case of the vaccination of particular patient groups, such as the immunocompromised and the elderly. In particular, developing vaccines against emerging viral pathogens adds a further level of complexity, as they may only be administered to small groups of people or only in response to a specific event or threat, limiting our ability to study and evaluate responses. In this commentary, we discuss how novel techniques may be used to engineer a new generation of vaccine candidates as we move toward a more targeted vaccine design strategy, driven by our understanding of the mechanisms of viral pathogenesis, attenuation and the signaling events which are required to develop a lasting, protective immunity. We will also briefly discuss the potential future role of vaccine adjuvants, which could be used to bridge the gap between vaccine safety, and lasting immunity from a single vaccination.
疫苗接种是目前医学上控制病毒性疾病最有效的策略。然而,研发疫苗是一个漫长且昂贵的过程,传统方法,如通过连续传代使野生型病毒减毒,可能并不适用于所有病毒,并且可能引发疫苗安全性方面的考量,特别是在为特定患者群体(如免疫功能低下者和老年人)接种疫苗的情况下。尤其是针对新出现的病毒病原体研发疫苗,会增加另一层面的复杂性,因为这些疫苗可能只能用于小部分人群,或者仅在应对特定事件或威胁时使用,这限制了我们研究和评估免疫反应的能力。在这篇评论中,我们将探讨在我们朝着更具针对性的疫苗设计策略迈进的过程中,如何利用新技术来设计新一代候选疫苗,这一策略是由我们对病毒发病机制、减毒以及产生持久保护性免疫所需的信号传导事件的理解所驱动的。我们还将简要讨论疫苗佐剂未来可能发挥的作用,其可用于弥合疫苗安全性与单次接种产生持久免疫之间的差距。