Abstract |
When labeled using the Iodogen method, a chimeric antibody composed of the human IgG2 constant region and the variable regions of murine anti- tenascin 81C6 exhibited superior uptake in human glioma xenografts compared with its murine parent. In the current study, three paired-label experiments were performed in athymic mice with subcutaneous D-54 MG human glioma xenografts to evaluate further the properties of radioiodinated chimeric 81C6. These studies demonstrated that (a) the enhanced tumor uptake of chimeric 81C6 is specific; (b) when labeling was performed using N-succinimidyl 3-iodobenzoate, chimeric 81C6 again showed preferential accumulation in tumor compared with murine 81C6; and (c) the tumor uptake advantage observed previously with murine 81C6 for N-succinimidyl 3-iodobenzoate compared with Iodogen labeling did not occur with chimeric 81C6.
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Authors | M R Zalutsky, G E Archer, P K Garg, S K Batra, D D Bigner |
Journal | Nuclear medicine and biology
(Nucl Med Biol)
Vol. 23
Issue 4
Pg. 449-58
(May 1996)
ISSN: 0969-8051 [Print] United States |
PMID | 8832699
(Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antibodies, Monoclonal
- Immunoglobulin G
- Immunotoxins
- Iodine Radioisotopes
- Recombinant Fusion Proteins
- Tenascin
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Topics |
- Animals
- Antibodies, Monoclonal
(pharmacokinetics)
- Brain Neoplasms
(metabolism)
- Glioma
(metabolism)
- Humans
- Immunoglobulin G
(metabolism)
- Immunotoxins
(pharmacokinetics)
- Iodine Radioisotopes
(pharmacokinetics)
- Isotope Labeling
- Mice
- Mice, Nude
- Neoplasm Transplantation
- Recombinant Fusion Proteins
(pharmacokinetics)
- Tenascin
(immunology)
- Tissue Distribution
- Transplantation, Heterologous
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