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PLoS One ; 13(5): e0197011, 2018.
Article de Anglais | MEDLINE | ID: mdl-29746518

RÉSUMÉ

Safe and effective antitoxins to treat and prevent botulism are needed for biodefense. We have developed recombinant antibody-based therapeutics for botulinum neurotoxin (BoNT) serotypes A, B, and E. The mechanism of action of this antitoxin requires that three mAbs bind one toxin molecule to achieve clearance. Here we present a co-formulation of an antitoxin to the three most important serotypes. Combining these antibodies obviates the need to identify the serotype causing intoxication prior to drug administration, which would facilitate administration. The lyophilized powder formulation contains nine mAbs, three mAbs for each of the three serotypes (A, B, E). The formulation was stored as a liquid and lyophilized powder for up to one year, and characterized by binding affinity and multiple physicochemical methods. No significant increase in soluble higher order aggregates, cleavage products, or change in charge isoforms was measured after storage as a lyophilized powder at 50°C for one year. Furthermore, toxin-domain binding ELISA data indicated that each of the individual antibodies in the lyophilized drug product showed essentially full binding capability to their respective toxin domains after being stored at 50°C for one year. Physicochemical characterization of the formulation demonstrated the nine individual mAbs were remarkably stable. This work demonstrates feasibility of lyophilized, oligoclonal antibody therapies for biodefense with ambient temperature stability, that would facilitate stockpiling, distribution, and administration.


Sujet(s)
Anticorps antibactériens/composition chimique , Anticorps monoclonaux/composition chimique , Antitoxine botulique/composition chimique , Toxines botuliniques de type A/antagonistes et inhibiteurs , Toxines botuliniques/antagonistes et inhibiteurs , Botulisme/immunologie , Anticorps antibactériens/immunologie , Anticorps monoclonaux/immunologie , Antitoxine botulique/immunologie , Toxines botuliniques/composition chimique , Toxines botuliniques/immunologie , Toxines botuliniques de type A/composition chimique , Toxines botuliniques de type A/immunologie , Botulisme/traitement médicamenteux , Température élevée , Humains , Stabilité protéique
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