Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases

نویسندگان

  • J. Rogers
  • R.J. Schoepp
  • O. Schröder
  • T.L. Clements
  • T.F. Holland
  • J.Q. Li
  • J. Li
  • L.M. Lewis
  • R.P. Dirmeier
  • G.J. Frey
  • X. Tan
  • K. Wong
  • G. Woodnutt
  • M. Keller
  • D.S. Reed
  • B.E. Kimmel
  • E.C. Tozer
چکیده

Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5-4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known.

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عنوان ژورنال:
  • Protein Engineering, Design and Selection

دوره 21  شماره 

صفحات  -

تاریخ انتشار 2008