Serwer Philip
Department of Biochemistry and Structural Biology, The University of Texas Health Center, San Antonio, TX 78229-3900, USA.
Vaccines (Basel). 2020 Oct 1;8(4):566. doi: 10.3390/vaccines8040566.
Rapid obtaining of safe, effective, anti-viral vaccines has recently risen to the top of the international agenda. To maximize the success probability of future anti-viral vaccines, the anti-viral vaccines successful in the past are summarized here by virus type and vaccine type. The primary focus is on viruses with both single-stranded RNA genomes and a membrane envelope, given the pandemic past of influenza viruses and coronaviruses. The following conclusion is reached, assuming that success of future strategies is positively correlated with strategies successful in the past. The primary strategy, especially for emerging pandemic viruses, should be development of vaccine antigens that are live-attenuated viruses; the secondary strategy should be development of vaccine antigens that are inactivated virus particles. Support for this conclusion comes from the complexity of immune systems. These conclusions imply the need for a revision in current strategic planning.
快速获得安全、有效的抗病毒疫苗最近已成为国际议程的首要任务。为了使未来抗病毒疫苗的成功概率最大化,本文按病毒类型和疫苗类型总结了过去成功的抗病毒疫苗。鉴于流感病毒和冠状病毒过去曾引发大流行,主要关注的是具有单链RNA基因组和膜包膜的病毒。假设未来策略的成功与过去成功的策略呈正相关,则得出以下结论。主要策略,特别是针对新出现的大流行病毒,应该是开发减毒活病毒疫苗抗原;次要策略应该是开发灭活病毒颗粒疫苗抗原。对这一结论的支持来自免疫系统的复杂性。这些结论意味着需要修订当前的战略规划。