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1 May 2003 Comparison of the Radiotoxicity of Two Alpha-Particle-Emitting Immunoconjugates, Terbium-149 and Bismuth-213, Directed against a Tumor-Specific, Exon 9 Deleted (d9) E-Cadherin Adhesion Protein
Matthias Miederer, Christof Seidl, Gerd-Jürgen Beyer, David E. Charlton, Sanja Vranjes-Duric, Jozef J. Comor, Roswitha Huber, Tuomo Nikula, Christos Apostolidis, Christoph Schuhmacher, Karl-Friedrich Becker, Reingard Senekowitsch-Schmidtke
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Abstract

Miederer, M., Seidl, C., Beyer, G-J., Charlton, D. E., Vranjes-Duric, S., Comor, J. J., Huber, R., Nikula, T., Apostolidis, C., Schuhmacher, C., Becker, K-F. and Senekowitsch-Schmidtke, R. Comparison of the Radiotoxicity of Two Alpha-Particle- Emitting Immunoconjugates, Terbium-149 and Bismuth-213, Directed against a Tumor-Specific, Exon 9 Deleted (d9) E-Cadherin Adhesion Protein. Radiat. Res. 159, 612–620 (2003).

We investigated the effects of the α-particle emitters 149Tb and 213Bi coupled to a tumor-specific antibody targeting the mutated delta 9 E-cadherin (d9 E-Cad) on single cells and cell pellets. The d9 mutation of the adhesion molecule E-cadherin is found in 10% of diffuse-type gastric cancers and is not expressed in normal tissue. Human breast cancer cells (MDA-MB-435S) transfected with d9 E-Cad or the wild-type E-cadherin gene were used to study the effects of anti-d9 E-Cad MAb coupled to 149Tb and 213Bi (149Tb-d9 MAb and 213Bi-d9 MAb). The density of binding sites determined on transfected MDA tumor cells by Scatchard analysis and flow cytometry varied from 4 × 104 to 6 × 104 antigens per cell. Internalization of radioimmunoconjugates by cells expressing d9 E-Cad was less than 10% of bound antibody within 240 min. The effect of the radioimmunoconjugates on cell suspensions and cell pellets was quantified by [3H]thymidine incorporation, and the dose to the cell nuclei was determined using microdosimetric calculations. 149Tb and 213Bi immunoconjugates affected cells in suspension similarly. Significant differences in the proliferation capacity of d9 E-cadherin- and wild-type E-cadherin-expressing cells were observed at activity concentrations around 185 kBq/ml, corresponding to antibody concentrations between 200 ng/ml and 1000 ng/ml. Proliferation after incubation with 213Bi-d9 MAb was 50% greater in pelleted wild-type E-Cad-expressing cells compared to wild-type E-Cad cells in suspension. In contrast, the proliferation of pelleted d9 E-Cad cells was similar to that of d9 E-Cad cells in suspension. For 149Tb-d9 MAb, no significant difference was found between pelleted cells and cells in suspension for low activity concentrations. However, at high activity concentrations, 149Tb-d9 MAb had only a small effect on pelleted cells. These in vitro studies demonstrate different effects of 149Tb and 213Bi conjugated to a tumor-specific antibody toward single cells and tumor cell pellets. Microdosimetric simulation of single cell survival after α-particle irradiation modeled the experimental results with reasonable accuracy.

Matthias Miederer, Christof Seidl, Gerd-Jürgen Beyer, David E. Charlton, Sanja Vranjes-Duric, Jozef J. Comor, Roswitha Huber, Tuomo Nikula, Christos Apostolidis, Christoph Schuhmacher, Karl-Friedrich Becker, and Reingard Senekowitsch-Schmidtke "Comparison of the Radiotoxicity of Two Alpha-Particle-Emitting Immunoconjugates, Terbium-149 and Bismuth-213, Directed against a Tumor-Specific, Exon 9 Deleted (d9) E-Cadherin Adhesion Protein," Radiation Research 159(5), 612-620, (1 May 2003). https://doi.org/10.1667/0033-7587(2003)159[0612:COTROT]2.0.CO;2
Received: 25 March 2002; Accepted: 1 October 2002; Published: 1 May 2003
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