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

PLoS One. 2016 Jul 18;11(7):e0159313. doi: 10.1371/journal.pone.0159313. eCollection 2016.

Abstract

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.

MeSH terms

  • Agrobacterium tumefaciens / genetics
  • Agrobacterium tumefaciens / metabolism
  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / biosynthesis*
  • Antibodies, Monoclonal / genetics
  • Antibodies, Viral / administration & dosage
  • Antibodies, Viral / biosynthesis*
  • Antibodies, Viral / genetics
  • Cloning, Molecular
  • Female
  • Gene Expression
  • Genetic Vectors / chemistry
  • Genetic Vectors / metabolism
  • Immunization, Passive*
  • Mesocricetus
  • Neutralization Tests
  • Nicotiana / genetics*
  • Nicotiana / metabolism
  • Plants, Genetically Modified
  • Rabies / immunology
  • Rabies / mortality
  • Rabies / prevention & control*
  • Rabies / virology
  • Rabies Vaccines / administration & dosage
  • Rabies Vaccines / biosynthesis
  • Rabies virus / drug effects
  • Rabies virus / growth & development
  • Rabies virus / immunology
  • Rabies virus / pathogenicity
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / genetics
  • Survival Analysis

Substances

  • Antibodies, Monoclonal
  • Antibodies, Viral
  • Rabies Vaccines
  • Recombinant Proteins

Grants and funding

LZ and KW are owners of Mapp Biopharmaceutical, a commercial company. MP is employed by Mapp Biopharmaceutical, while JM and SH are employed by Kentucky Bioprocessing, a commercial company. The authors thank the National Research Foundation (SB) (www.nrf.ac.za), Technology Innovation Agency (RC) (www.tia.org.za), the Agricultural Research Council Rabies Diagnostic Cost Centre (15/04/P001) (CS) and Council for Scientific and Industrial Research (SA) (TT, RC) (www.csir.co.za) for funding support. The funders provided support in the form of salaries for authors SB, TT and RC, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.