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Preloading with Unlabeled CA19.9 Targeted Human Monoclonal Antibody Leads to Improved PET Imaging with (89)Zr-5B1
[Image: see text] CA19.9 is one of the most commonly occurring and highest density antigens in >90% of pancreatic cancers, making it an excellent target for monoclonal antibody (mAb)-based imaging and therapy applications. Preloading of unlabeled antibodies to enhance targeting of a radiolabeled...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341702/ https://www.ncbi.nlm.nih.gov/pubmed/28191976 http://dx.doi.org/10.1021/acs.molpharmaceut.6b01130 |
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author | Houghton, Jacob L. Abdel-Atti, Dalya Scholz, Wolfgang W. Lewis, Jason S. |
author_facet | Houghton, Jacob L. Abdel-Atti, Dalya Scholz, Wolfgang W. Lewis, Jason S. |
author_sort | Houghton, Jacob L. |
collection | PubMed |
description | [Image: see text] CA19.9 is one of the most commonly occurring and highest density antigens in >90% of pancreatic cancers, making it an excellent target for monoclonal antibody (mAb)-based imaging and therapy applications. Preloading of unlabeled antibodies to enhance targeting of a radiolabeled mAb has been previously described both for imaging and radioimmunotherapy studies for other targets. We investigated the effect of preloading with the unmodified anti-CA19.9 antibody 5B1 on the uptake and contrast of the PET tracer (89)Zr-5B1 in subcutaneous and orthotopic murine models of pancreatic cancer utilizing Capan-2 xenografts, known to both express CA19.9 and shed antigen into circulation. Biodistribution and PET imaging studies with (89)Zr-5B1 alone showed high levels in the liver, spleen, and lymph nodes of mice with subcutaneous Capan-2 tumor xenografts when administered without preinjection of 5B1. When unlabeled 5B1 was administered prior to (89)Zr-5B1, the tracer significantly enhanced image contrast and tumor to tissue ratios in the same model, and the improvement was related to the time interval between the injections. Moreover, tumors were clearly delineated in an orthotopic pancreatic cancer model using our optimized approach. Taken together, these data suggest that preloading with 5B1 can improve (89)Zr-5B1 imaging of disease in a Capan-2 mouse model and that exploration of preloading may have clinical utility for ongoing clinical investigations. |
format | Online Article Text |
id | pubmed-5341702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-53417022018-02-13 Preloading with Unlabeled CA19.9 Targeted Human Monoclonal Antibody Leads to Improved PET Imaging with (89)Zr-5B1 Houghton, Jacob L. Abdel-Atti, Dalya Scholz, Wolfgang W. Lewis, Jason S. Mol Pharm [Image: see text] CA19.9 is one of the most commonly occurring and highest density antigens in >90% of pancreatic cancers, making it an excellent target for monoclonal antibody (mAb)-based imaging and therapy applications. Preloading of unlabeled antibodies to enhance targeting of a radiolabeled mAb has been previously described both for imaging and radioimmunotherapy studies for other targets. We investigated the effect of preloading with the unmodified anti-CA19.9 antibody 5B1 on the uptake and contrast of the PET tracer (89)Zr-5B1 in subcutaneous and orthotopic murine models of pancreatic cancer utilizing Capan-2 xenografts, known to both express CA19.9 and shed antigen into circulation. Biodistribution and PET imaging studies with (89)Zr-5B1 alone showed high levels in the liver, spleen, and lymph nodes of mice with subcutaneous Capan-2 tumor xenografts when administered without preinjection of 5B1. When unlabeled 5B1 was administered prior to (89)Zr-5B1, the tracer significantly enhanced image contrast and tumor to tissue ratios in the same model, and the improvement was related to the time interval between the injections. Moreover, tumors were clearly delineated in an orthotopic pancreatic cancer model using our optimized approach. Taken together, these data suggest that preloading with 5B1 can improve (89)Zr-5B1 imaging of disease in a Capan-2 mouse model and that exploration of preloading may have clinical utility for ongoing clinical investigations. American Chemical Society 2017-02-13 2017-03-06 /pmc/articles/PMC5341702/ /pubmed/28191976 http://dx.doi.org/10.1021/acs.molpharmaceut.6b01130 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Houghton, Jacob L. Abdel-Atti, Dalya Scholz, Wolfgang W. Lewis, Jason S. Preloading with Unlabeled CA19.9 Targeted Human Monoclonal Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title | Preloading with Unlabeled CA19.9 Targeted Human Monoclonal
Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title_full | Preloading with Unlabeled CA19.9 Targeted Human Monoclonal
Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title_fullStr | Preloading with Unlabeled CA19.9 Targeted Human Monoclonal
Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title_full_unstemmed | Preloading with Unlabeled CA19.9 Targeted Human Monoclonal
Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title_short | Preloading with Unlabeled CA19.9 Targeted Human Monoclonal
Antibody Leads to Improved PET Imaging with (89)Zr-5B1 |
title_sort | preloading with unlabeled ca19.9 targeted human monoclonal
antibody leads to improved pet imaging with (89)zr-5b1 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341702/ https://www.ncbi.nlm.nih.gov/pubmed/28191976 http://dx.doi.org/10.1021/acs.molpharmaceut.6b01130 |
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