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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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. |
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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0197011</identifier><identifier>PMID: 29746518</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2018-05, Vol.13 (5), p.e0197011</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 Li et al 2018 Li et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-71ffdb478d69d4979e5fe371d39f9ccf1d674fea851d07d142329c3e039a9e6a3</citedby><cites>FETCH-LOGICAL-c692t-71ffdb478d69d4979e5fe371d39f9ccf1d674fea851d07d142329c3e039a9e6a3</cites><orcidid>0000-0003-4130-6332</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944936/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944936/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29746518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Goldman, Ellen R.</contributor><creatorcontrib>Li, Mingxiang</creatorcontrib><creatorcontrib>Lee, Dennis</creatorcontrib><creatorcontrib>Obi, Chidi R</creatorcontrib><creatorcontrib>Freeberg, Joel K</creatorcontrib><creatorcontrib>Farr-Jones, Shauna</creatorcontrib><creatorcontrib>Tomic, Milan T</creatorcontrib><title>An ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>Ambient temperature</subject><subject>Antibodies</subject><subject>Antibodies, Bacterial - chemistry</subject><subject>Antibodies, Bacterial - immunology</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antitoxins</subject><subject>Binding</subject><subject>Biology and Life Sciences</subject><subject>Botulinum Antitoxin - chemistry</subject><subject>Botulinum Antitoxin - immunology</subject><subject>Botulinum toxin</subject><subject>Botulinum Toxins - antagonists & inhibitors</subject><subject>Botulinum Toxins - chemistry</subject><subject>Botulinum Toxins - immunology</subject><subject>Botulinum Toxins, Type A - antagonists & inhibitors</subject><subject>Botulinum Toxins, Type A - chemistry</subject><subject>Botulinum Toxins, Type A - immunology</subject><subject>Botulism</subject><subject>Botulism - drug therapy</subject><subject>Botulism - immunology</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Feasibility studies</subject><subject>Food contamination</subject><subject>Hot Temperature</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunotherapy</subject><subject>Intoxication</subject><subject>Isoforms</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Molecular chains</subject><subject>Monoclonal antibodies</subject><subject>Neurotoxins</subject><subject>Powder</subject><subject>Protein Stability</subject><subject>Proteins</subject><subject>Recombinant molecules</subject><subject>Research and Analysis Methods</subject><subject>Serotypes</subject><subject>Temperature</subject><subject>Toxins</subject><subject>Water-borne diseases</subject><subject>Waterborne 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ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E</title><author>Li, Mingxiang ; Lee, Dennis ; Obi, Chidi R ; Freeberg, Joel K ; Farr-Jones, Shauna ; Tomic, Milan T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-71ffdb478d69d4979e5fe371d39f9ccf1d674fea851d07d142329c3e039a9e6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Ambient temperature</topic><topic>Antibodies</topic><topic>Antibodies, Bacterial - chemistry</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antibodies, Monoclonal - chemistry</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antitoxins</topic><topic>Binding</topic><topic>Biology and Life Sciences</topic><topic>Botulinum Antitoxin - chemistry</topic><topic>Botulinum Antitoxin - immunology</topic><topic>Botulinum toxin</topic><topic>Botulinum Toxins - 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titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Mingxiang</au><au>Lee, Dennis</au><au>Obi, Chidi R</au><au>Freeberg, Joel K</au><au>Farr-Jones, Shauna</au><au>Tomic, Milan T</au><au>Goldman, Ellen R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An ambient temperature-stable antitoxin of nine co-formulated antibodies for botulism caused by serotypes A, B and E</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-05-10</date><risdate>2018</risdate><volume>13</volume><issue>5</issue><spage>e0197011</spage><pages>e0197011-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><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.</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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T00%3A11%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20ambient%20temperature-stable%20antitoxin%20of%20nine%20co-formulated%20antibodies%20for%20botulism%20caused%20by%20serotypes%20A,%20B%20and%20E&rft.jtitle=PloS%20one&rft.au=Li,%20Mingxiang&rft.date=2018-05-10&rft.volume=13&rft.issue=5&rft.spage=e0197011&rft.pages=e0197011-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0197011&rft_dat=%3Cgale_plos_%3EA538070141%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2037055374&rft_id=info:pmid/29746518&rft_galeid=A538070141&rft_doaj_id=oai_doaj_org_article_177f16fd05a148df946f5fe7204ad200&rfr_iscdi=true |