Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Tumor Immunology: New Perspectives
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 49, 5543-5549, October 15, 1989]
© 1989 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zalutsky, M. R.
Right arrow Articles by Bigner, D. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zalutsky, M. R.
Right arrow Articles by Bigner, D. D.

Enhanced Tumor Localization and in Vivo Stability of a Monoclonal Antibody Radioiodinated Using N-Succinimidyl 3-(Tri-n-butylstannyl)benzoate1

Michael R. Zalutsky2, Michael A. Noska, Edward V. Colapinto, Pradeep K. Garg and Darell D. Bigner

Departments of Radiology [M. R. Z., M. A. N., P. K. G.] and Pathology [E. V. C., D. D. B.] and the Preuss Laboratory for Brain Tumor Research [D. D. B.], Duke University Medical Center, Durham, North Carolina 27710

Loss of radiolabel after in vivo administration of labeled monoclonal antibodies (MAbs) to cancer patients is a likely cause of the low levels of tumor uptake of MAb which have been observed. In this study, we have evaluated the utility of N-succinimidyl 3-(tri-n-butylstannyl)benzoate (ATE) for the radioiodination of 81C6, a MAb reactive with the extracellular matrix antigen tenascin associated with gliomas and other tumors. In vitro binding properties of MAb labeled via ATE were slightly better than those of the Iodogen preparations. Paired-label studies were performed in athymic mice bearing s.c. D-54 MG xenografts and injected with both 81C6 labeled with 125I using the ATE method and 131I using the Iodogen method. These studies demonstrated that use of the ATE method (a) decreased thyroid uptake by 40- to 100-fold, suggesting a lower rate of dehalogenation compared to MAb labeled using Iodogen; (b) increased tumor uptake by as much as a factor of 4 at Day 1 to more than 12-fold at Day 8; and (c) resulted in superior tumor-to-normal-tissue dose ratios. The specificity of MAb uptake was investigated in a paired-labeled study comparing the distribution of 81C6 and isotype-matched control 45.6, both labeled using the ATE procedure. Localization indices for tumor ranged between 6 at Day 1 to 34 at Day 7, values considerably higher than those reported previously for 81C6 and 45.6 radioiodinated using a conventional method (chloramine T). These results demonstrate that the ATE method may be a valuable approach for labeling MAbs with iodine nuclides.

1 Supported by National Cancer Institute Grants CA 42324, CA 11898, CA 43638, 5-P50-NS 20023, and 5-P30-CA 14236.

2 To whom requests for reprints should be addressed, at Department of Radiology, Duke University Medical Center, Box 3808, Durham, NC 27710.

Received 3/20/89. Revised 7/ 7/89. Accepted 7/20/89.




This article has been cited by other articles:


Home page
BloodHome page
D. A. Rizzieri, G. Akabani, M. R. Zalutsky, R. E. Coleman, S. D. Metzler, J. E. Bowsher, B. Toaso, E. Anderson, A. Lagoo, S. Clayton, et al.
Phase 1 trial study of 131I-labeled chimeric 81C6 monoclonal antibody for the treatment of patients with non-Hodgkin lymphoma
Blood, August 1, 2004; 104(3): 642 - 648.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
Z. Cheng, J. Chen, T. P. Quinn, and S. S. Jurisson
Radioiodination of Rhenium Cyclized {alpha}-Melanocyte-Stimulating Hormone Resulting in Enhanced Radioactivity Localization and Retention in Melanoma
Cancer Res., February 15, 2004; 64(4): 1411 - 1418.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1989 by the American Association for Cancer Research.