1. Academic Validation
  2. SYN023, a novel humanized monoclonal antibody cocktail, for post-exposure prophylaxis of rabies

SYN023, a novel humanized monoclonal antibody cocktail, for post-exposure prophylaxis of rabies

  • PLoS Negl Trop Dis. 2017 Dec 20;11(12):e0006133. doi: 10.1371/journal.pntd.0006133.
Tzu-Yuan Chao 1 Shiqi Ren 1 Enyun Shen 2 Susan Moore 3 Shou-Feng Zhang 4 Li Chen 1 Charles E Rupprecht 5 Eric Tsao 1
Affiliations

Affiliations

  • 1 Synermore Biologics Co., Ltd., Taipei, Taiwan.
  • 2 Beijing Cotimes Biotech Co., Ltd., Beijing, China.
  • 3 Kansas State University Rabies Laboratory, Manhattan, Kansas State, United States of America.
  • 4 Laboratory of Epidemiology and Key Laboratory of Jilin Provincial Zoonosis Control and Prevention, Military Veterinary Research Institute, Academy of Military Medical Sciences, Changchun, China.
  • 5 LYSSA LLC, Atlanta, Georgia, United States of America.
Abstract

Rabies is a neglected zoonotic disease that is preventable in humans by appropriate post-exposure prophylaxis (PEP). However, current PEP relies on polyclonal immune globulin products purified from pooled human (HRIG) or equine (ERIG) plasma that are either in chronic shortage or in association with safety concerns. Here, we present the development of an antibody cocktail, SYN023, made of two novel monoclonal Antibodies (MAb) CTB011 and CTB012 that could serve as safer and more cost-effective alternatives to the current RIG products. Both CTB011 and CTB012 are humanized MAbs that bind to non-overlapping epitopes on the rabies virus (RABV) glycoprotein (G) with sub-nanomolar affinities. Sequence analysis revealed that many of the critical residues in binding are highly conserved across different species of lyssaviruses. When combined at a 1:1 ratio, CTB011/CTB012 exhibited neutralization capabilities equivalent or superior to HRIG against 10 North American street RABV isolates in vitro and 15 prevalent Chinese RABV strains in animal models. Finally, SYN023, at a dosage of 0.03 mg/kg, was able to offer the same degree of protection as standard HRIG administration (20 IU/kg) in Syrian hamsters challenged with a highly virulent bat (Tadarida brasiliensis) RABV variant. Taken together, the high-potency and broad-spectrum neutralization demonstrated by SYN023 make it an effective candidate for human rabies PEP consideration.

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