In Vivo Kinetics of Radiolabeled Monoclonal Anti-CEA Antibodies in Animal Models

• Published in: The Journal of nuclear medicine (1978) Vol. 26; no. 12; pp. 1418 - 1423
• Main Authors: Hagan, Phillip L, Halpern, Samuel E, Chen, Agnes, Krishnan, Lakshmy, Frincke, James, Bartholomew, Richard M, David, Gary S, Carlo, Dennis
• Format: Journal Article
• Language: English
• Published: United States Soc Nuclear Med 01-12-1985
• Subjects: Animals; Antibodies, Monoclonal - immunology; Antigen-Antibody Complex; Carcinoembryonic Antigen - immunology; Colonic Neoplasms - immunology; Humans; Hybridomas - immunology; Indium; Iodine Radioisotopes; Kinetics; Liver - diagnostic imaging; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasm Transplantation; Radioisotopes; Radionuclide Imaging; Spleen - diagnostic imaging
• ISSN: 0161-5505; 1535-5667

Studies were performed to determine the effect of the radiolabel and circulating carcinoembryonic antigen (CEA) on the pharmacodynamics of monoclonal anti-CEA antibodies (MoAbs). The studies were performed in normal BALB/c mice and in nude mice bearing human colon tumors. Three different tumors were used, each of which produced CEA levels characteristic of that particular tumor's secretory rate. The CEJ-326 MoAb labeled with either 111In or 125I was used in all studies. Circulating CEA induced the removal of 125I and 111In MoAbs from the vascular compartment. Liver concentrations of 111In increased and 125I levels decreased as the CEA secretory rate of the tumor rose. This indicates that circulating CEA complexes form in the vascular compartment which, in an animal model, are removed by the liver and spleen. This results in decreased tumor uptake of the labeled MoAb. The iodinated MoAb complexes are dehalogenated while the 111In is retained by the liver. This dehalogenation may account for the relatively low liver activity observed in radioimmunoimaging with intact radioiodinated anti-CEA MoAbs, provided the CEA complexes are similarly removed from the vascular compartment by the human liver.