Frontiers in Cellular and Infection Microbiology (Jul 2021)

Developing Recombinant Antibodies by Phage Display Against Infectious Diseases and Toxins for Diagnostics and Therapy

  • Kristian Daniel Ralph Roth,
  • Esther Veronika Wenzel,
  • Esther Veronika Wenzel,
  • Maximilian Ruschig,
  • Stephan Steinke,
  • Nora Langreder,
  • Philip Alexander Heine,
  • Kai-Thomas Schneider,
  • Rico Ballmann,
  • Viola Fühner,
  • Philipp Kuhn,
  • Thomas Schirrmann,
  • André Frenzel,
  • Stefan Dübel,
  • Stefan Dübel,
  • Stefan Dübel,
  • Maren Schubert,
  • Gustavo Marçal Schmidt Garcia Moreira,
  • Federico Bertoglio,
  • Giulio Russo,
  • Giulio Russo,
  • Michael Hust,
  • Michael Hust

DOI
https://doi.org/10.3389/fcimb.2021.697876
Journal volume & issue
Vol. 11

Abstract

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Antibodies are essential molecules for diagnosis and treatment of diseases caused by pathogens and their toxins. Antibodies were integrated in our medical repertoire against infectious diseases more than hundred years ago by using animal sera to treat tetanus and diphtheria. In these days, most developed therapeutic antibodies target cancer or autoimmune diseases. The COVID-19 pandemic was a reminder about the importance of antibodies for therapy against infectious diseases. While monoclonal antibodies could be generated by hybridoma technology since the 70ies of the former century, nowadays antibody phage display, among other display technologies, is robustly established to discover new human monoclonal antibodies. Phage display is an in vitro technology which confers the potential for generating antibodies from universal libraries against any conceivable molecule of sufficient size and omits the limitations of the immune systems. If convalescent patients or immunized/infected animals are available, it is possible to construct immune phage display libraries to select in vivo affinity-matured antibodies. A further advantage is the availability of the DNA sequence encoding the phage displayed antibody fragment, which is packaged in the phage particles. Therefore, the selected antibody fragments can be rapidly further engineered in any needed antibody format according to the requirements of the final application. In this review, we present an overview of phage display derived recombinant antibodies against bacterial, viral and eukaryotic pathogens, as well as microbial toxins, intended for diagnostic and therapeutic applications.

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