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dc.contributor.authorDou, Shuping
dc.contributor.authorVirostko, John
dc.contributor.authorRusckowski, Mary
dc.contributor.authorGreiner, Dale L.
dc.contributor.authorPowers, Alvin C.
dc.contributor.authorLiu, Guozheng
dc.date2022-08-11T08:10:47.000
dc.date.accessioned2022-08-23T17:20:16Z
dc.date.available2022-08-23T17:20:16Z
dc.date.issued2014-07-24
dc.date.submitted2014-11-17
dc.identifier.citationFront Pharmacol. 2014 Jul 24;5:172. doi: 10.3389/fphar.2014.00172. <a href="http://dx.doi.org/10.3389/fphar.2014.00172">Link to article on publisher's site</a>
dc.identifier.issn1663-9812 (Electronic)
dc.identifier.doi10.3389/fphar.2014.00172
dc.identifier.pmid25104938
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48266
dc.description.abstractAlthough an increasing number of antibody conjugates are being used in the clinic, there remain many unmet needs in antibody targeting. Normal tissue background is one of the key issues that limits the therapeutic efficacy and the detection sensitivity. Background reduction coupled with dose increase may provide the required target accumulation of the label or toxin at an acceptable normal tissue background. However, the knowledge about the in vivo interaction between antibody and a clearing agent is currently inadequate for designing a rational clearance regimen or system. The current investigation focuses on the clearability of antibody for background reduction, an important topic to antibody targeting in general. The investigation employs pretargeting as a research tool and avidin as a model clearing agent. By comparing the effects of natural clearance at a longer post-injection time and avidin clearance, we demonstrated that avidin clearance is much more effective. By directly attaching avidin to a biotinylated antibody prior to injection, we found that the biotinylated antibody in blood, once bound to the clearing agent, can be removed from the circulation immediately and completely, while the real non-clearable antibody without biotin stays. The study of multiple avidin injections confirmed that the presence of clearable biotinylated antibodies after an avidin injection is due to their temporary inaccessibility and subsequent return from tissue compartments. The collective clearance efficiency of 91% by three avidin injections indicates a continuous IV infusion would be recommended to remove all of the biotinylated IgG molecules. In conclusion, the use of antibody pretargeting as a tool in this study has improved understanding of the incomplete clearance by avidin and can aid in overcoming this obstacle.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=25104938&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsCopyright © 2014 Dou, Virostko, Rusckowski, Greiner, Powers and Liu. This is an open-access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by/3.0/" target="_blank">Creative Commons Attribution License (CC BY)</a>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.subjectpretargeting
dc.subjectantibody
dc.subjectclearingagent
dc.subjectavidin
dc.subjectin vivo accessibility
dc.subjectimmunotargeting
dc.subjectMedical Pharmacology
dc.subjectMedicinal and Pharmaceutical Chemistry
dc.subjectMedicinal Chemistry and Pharmaceutics
dc.subjectRadiology
dc.subjectTherapeutics
dc.titleDifferentiation between temporary and real non-clearability of biotinylated IgG antibody by avidin in mice
dc.typeJournal Article
dc.source.journaltitleFrontiers in pharmacology
dc.source.volume5
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1037&amp;context=radiology_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/radiology_pubs/38
dc.identifier.contextkey6367418
refterms.dateFOA2022-08-23T17:20:17Z
html.description.abstract<p>Although an increasing number of antibody conjugates are being used in the clinic, there remain many unmet needs in antibody targeting. Normal tissue background is one of the key issues that limits the therapeutic efficacy and the detection sensitivity. Background reduction coupled with dose increase may provide the required target accumulation of the label or toxin at an acceptable normal tissue background. However, the knowledge about the in vivo interaction between antibody and a clearing agent is currently inadequate for designing a rational clearance regimen or system. The current investigation focuses on the clearability of antibody for background reduction, an important topic to antibody targeting in general. The investigation employs pretargeting as a research tool and avidin as a model clearing agent. By comparing the effects of natural clearance at a longer post-injection time and avidin clearance, we demonstrated that avidin clearance is much more effective. By directly attaching avidin to a biotinylated antibody prior to injection, we found that the biotinylated antibody in blood, once bound to the clearing agent, can be removed from the circulation immediately and completely, while the real non-clearable antibody without biotin stays. The study of multiple avidin injections confirmed that the presence of clearable biotinylated antibodies after an avidin injection is due to their temporary inaccessibility and subsequent return from tissue compartments. The collective clearance efficiency of 91% by three avidin injections indicates a continuous IV infusion would be recommended to remove all of the biotinylated IgG molecules. In conclusion, the use of antibody pretargeting as a tool in this study has improved understanding of the incomplete clearance by avidin and can aid in overcoming this obstacle.</p>
dc.identifier.submissionpathradiology_pubs/38
dc.contributor.departmentDepartment of Molecular Medicine
dc.contributor.departmentDepartment of Radiology
dc.source.pages172


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Copyright © 2014 Dou, Virostko, Rusckowski, Greiner, Powers and Liu. This is an open-access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by/3.0/" target="_blank">Creative Commons Attribution License (CC BY)</a>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as Copyright © 2014 Dou, Virostko, Rusckowski, Greiner, Powers and Liu. This is an open-access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by/3.0/" target="_blank">Creative Commons Attribution License (CC BY)</a>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.