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High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries.

Ing-Chien ChenYi-Kai ChiuChung-Ming YuCheng-Chung LeeChao-Ping TungYueh-Liang TsouYi-Jen HuangChia-Lung LinHong-Sen ChenAndrew H-J WangAn-Suei Yang
Published in: Scientific reports (2017)
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.
Keyphrases
  • high throughput
  • dengue virus
  • sars cov
  • single cell
  • endothelial cells
  • small molecule
  • pseudomonas aeruginosa
  • zika virus
  • early onset
  • cystic fibrosis
  • working memory
  • mass spectrometry
  • monoclonal antibody