Genomics Research Center, Academia Sinica, 115, Taipei, Taiwan.
Institute of Biological Chemistry, Academia Sinica, 115, Taipei, Taiwan.
Sci Rep. 2017 Oct 31;7(1):14455. doi: 10.1038/s41598-017-14823-w.
Pandemic and epidemic outbreaks of influenza A virus (IAV) infection pose severe challenges to human society. Passive immunotherapy with recombinant neutralizing antibodies can potentially mitigate the threats of IAV infection. With a high throughput neutralizing antibody discovery platform, we produced artificial anti-hemagglutinin (HA) IAV-neutralizing IgGs from phage-displayed synthetic scFv libraries without necessitating prior memory of antibody-antigen interactions or relying on affinity maturation essential for in vivo immune systems to generate highly specific neutralizing antibodies. At least two thirds of the epitope groups of the artificial anti-HA antibodies resemble those of natural protective anti-HA antibodies, providing alternatives to neutralizing antibodies from natural antibody repertoires. With continuing advancement in designing and constructing synthetic scFv libraries, this technological platform is useful in mitigating not only the threats of IAV pandemics but also those from other newly emerging viral infections.
流感病毒(IAV)感染的大流行和爆发对人类社会构成了严峻挑战。使用重组中和抗体的被动免疫疗法可能减轻 IAV 感染的威胁。我们利用高通量中和抗体发现平台,从噬菌体展示的合成 scFv 文库中产生了人工抗血凝素(HA)IAV 中和 IgG,而无需预先记忆抗体-抗原相互作用,也无需依赖体内免疫系统进行亲和力成熟来产生高度特异性的中和抗体。人工抗 HA 抗体的至少三分之二的表位组类似于天然保护性抗 HA 抗体的表位组,为中和抗体提供了来自天然抗体库的替代品。随着设计和构建合成 scFv 文库技术的不断进步,该技术平台不仅可用于减轻 IAV 大流行的威胁,也可用于减轻其他新出现的病毒感染的威胁。