Isolation of nanomolar scFvs of non-human primate origin, cross-neutralizing botulinum neurotoxins A1 and A2 by targeting their heavy chain

BMC Biotechnology

Research Article

Dorothea Sesardic¹  Christine Rasetti-Escargueil¹  Arnaud Avril²  Philippe Thullier²  Siham Chahboun²  Thibaut Pelat³  Michel R. Popoff⁴  Christelle Mazuet⁴  Sebastian Miethe⁵  Michael Hust⁵ 

[1] Division of Bacteriology, National Institute for Biological Standards and Control (NIBSC), a centre of Medicines and Healthcare products Regulatory Agency, Blanche Lane, South Mimms, Potters Bar, EN6 3QG, Hertfordshire, UK;Département des Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, Unité Interaction Hôte-Pathogène, 1 Place du Général Valérie André, BP73, 91220, Brétigny-sur-Orge, CEDEX, France;Département des Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, Unité Interaction Hôte-Pathogène, 1 Place du Général Valérie André, BP73, 91220, Brétigny-sur-Orge, CEDEX, France;BIOTEM, Parc d’activité Bièvre Dauphine 885, rue Alphonse Gourju, 38140, Apprieu, France;Institut Pasteur, Centre National de Référence des bactéries anaérobies et du botulisme, 75724, Paris, France;Technische Universität Braunschweig, Institut für Biochemie, Biotechnologie und Bioinformatik, Abteilung Biotechnologie, Spielmannstr. 7, 38106, Braunschweig, Germany;

关键词: Botulinum neurotoxin;    Recombinant antibodies;    scFv;    Neutralizing antibodies;    Non-human primates;    Clostridium botulinum;    AntiBotABE;    Macaques;    Biological warfare agents;   

DOI  :  10.1186/s12896-015-0206-0

 received in 2014-12-10, accepted in 2015-09-11,  发布年份 2015

来源: Springer

【 摘 要 】

BackgroundBotulism is a naturally occurring disease, mainly caused by the ingestion of food contaminated by the botulinum neurotoxins (BoNTs). Botulinum neurotoxins are the most lethal. They are classified among the six major biological warfare agents by the Centers for Disease Control. BoNTs act on the cholinergic motoneurons, where they cleave proteins implicated in acetylcholine vesicle exocytosis. This exocytosis inhibition induces a flaccid paralysis progressively affecting all the muscles and generally engendering a respiratory distress. BoNTs are also utilized in medicine, mainly for the treatment of neuromuscular disorders, preventing large scale vaccination. Botulism specific treatment requires injections of antitoxins, usually of equine origin and thus poorly tolerated. Therefore, development of human or human-like neutralizing antibodies is of a major interest, and it is the subject of the European framework project called “AntiBotABE”.ResultsIn this study, starting from a macaque immunized with the recombinant heavy chain of BoNT/A1 (BoNT/A1-HC), an immune antibody phage-display library was generated and antibody fragments (single chain Fragment variable) with nanomolar affinity were isolated and further characterized. The neutralization capacities of these scFvs were analyzed in the mouse phrenic nerve-hemidiaphragm assay.ConclusionsAfter a three-round panning, 24 antibody fragments with affinity better than 10 nM were isolated. Three of them neutralized BoNT/A1 efficiently and two cross-neutralized BoNT/A1 and BoNT/A2 subtypes in the mouse phrenic nerve-hemidiaphragm assay. These are the first monoclonal human-like antibodies cross-neutralizing both BoNT/A1 and BoNT/A2. The antibody A1HC38 was selected for further development, and could be clinically developed for the prophylaxis and treatment of botulism.

【 授权许可】

CC BY   
© Avril et al. 2015