An ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E

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 achiev...

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Veröffentlicht in:PloS one 2018-05, Vol.13 (5), p.e0197011
Hauptverfasser: Li, Mingxiang, Lee, Dennis, Obi, Chidi R, Freeberg, Joel K, Farr-Jones, Shauna, Tomic, Milan T
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creator Li, Mingxiang
Lee, Dennis
Obi, Chidi R
Freeberg, Joel K
Farr-Jones, Shauna
Tomic, Milan T
description 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.
doi_str_mv 10.1371/journal.pone.0197011
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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. 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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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29746518</pmid><doi>10.1371/journal.pone.0197011</doi><tpages>e0197011</tpages><orcidid>https://orcid.org/0000-0003-4130-6332</orcidid><oa>free_for_read</oa></addata></record>
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subjects Ambient temperature
Antibodies
Antibodies, Bacterial - chemistry
Antibodies, Bacterial - immunology
Antibodies, Monoclonal - chemistry
Antibodies, Monoclonal - immunology
Antitoxins
Binding
Biology and Life Sciences
Botulinum Antitoxin - chemistry
Botulinum Antitoxin - immunology
Botulinum toxin
Botulinum Toxins - antagonists & inhibitors
Botulinum Toxins - chemistry
Botulinum Toxins - immunology
Botulinum Toxins, Type A - antagonists & inhibitors
Botulinum Toxins, Type A - chemistry
Botulinum Toxins, Type A - immunology
Botulism
Botulism - drug therapy
Botulism - immunology
Cancer
Care and treatment
Enzyme-linked immunosorbent assay
Feasibility studies
Food contamination
Hot Temperature
Humans
Immunoglobulins
Immunotherapy
Intoxication
Isoforms
Medical research
Medicine and Health Sciences
Molecular chains
Monoclonal antibodies
Neurotoxins
Powder
Protein Stability
Proteins
Recombinant molecules
Research and Analysis Methods
Serotypes
Temperature
Toxins
Water-borne diseases
Waterborne diseases
Yeast
title An ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E
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