PLoS ONE (Jan 2016)

Efficient In Vitro and In Vivo Activity of Glyco-Engineered Plant-Produced Rabies Monoclonal Antibodies E559 and 62-71-3.

  • Tsepo Lebiletsa Tsekoa,
  • Therese Lotter-Stark,
  • Sindisiwe Buthelezi,
  • Ereck Chakauya,
  • Stoyan H Stoychev,
  • Claude Sabeta,
  • Wonderful Shumba,
  • Baby Phahladira,
  • Steve Hume,
  • Josh Morton,
  • Charles E Rupprecht,
  • Herta Steinkellner,
  • Michael Pauly,
  • Larry Zeitlin,
  • Kevin Whaley,
  • Rachel Chikwamba

DOI
https://doi.org/10.1371/journal.pone.0159313
Journal volume & issue
Vol. 11, no. 7
p. e0159313

Abstract

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Rabies is a neglected zoonotic disease that has no effective treatment after onset of illness. However the disease can be prevented effectively by prompt administration of post exposure prophylaxis which includes administration of passive immunizing antibodies (Rabies Immune Globulin, RIG). Currently, human RIG suffers from many restrictions including limited availability, batch-to batch inconsistencies and potential for contamination with blood-borne pathogens. Anti-rabies monoclonal antibodies (mAbs) have been identified as a promising alternative to RIG. Here, we applied a plant-based transient expression system to achieve rapid, high level production and efficacy of the two highly potent anti-rabies mAbs E559 and 62-71-3. Expression levels of up to 490 mg/kg of recombinant mAbs were obtained in Nicotiana benthamiana glycosylation mutants by using a viral based transient expression system. The plant-made E559 and 62-71-3, carrying human-type fucose-free N-glycans, assembled properly and were structurally sound as determined by mass spectrometry and calorimetric density measurements. Both mAbs efficiently neutralised diverse rabies virus variants in vitro. Importantly, E559 and 62-71-3 exhibited enhanced protection against rabies virus compared to human RIG in a hamster model post-exposure challenge trial. Collectively, our results provide the basis for the development of a multi-mAb based alternative to RIG.