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An ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E.
Li, Mingxiang; Lee, Dennis; Obi, Chidi R; Freeberg, Joel K; Farr-Jones, Shauna; Tomic, Milan T.
Afiliação
  • Li M; XOMA Corp., Berkeley, CA, United States of America.
  • Lee D; XOMA Corp., Berkeley, CA, United States of America.
  • Obi CR; XOMA Corp., Berkeley, CA, United States of America.
  • Freeberg JK; XOMA Corp., Berkeley, CA, United States of America.
  • Farr-Jones S; Department of Anesthesia and Perioperative Care, University of California, San Francisco, San Francisco, CA, United States of America.
  • Tomic MT; XOMA Corp., Berkeley, CA, United States of America.
PLoS One ; 13(5): e0197011, 2018.
Article em En | MEDLINE | ID: mdl-29746518
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas / Botulismo / Antitoxina Botulínica / Toxinas Botulínicas Tipo A / Anticorpos Antibacterianos / Anticorpos Monoclonais Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas / Botulismo / Antitoxina Botulínica / Toxinas Botulínicas Tipo A / Anticorpos Antibacterianos / Anticorpos Monoclonais Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article