| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
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:
![]() |
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] |
||||
![]() |
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 |