Abstract:Summary.-Monoclonal antibodies to epithelial -cell antigenic determinants, labelled with 1231 and 1251, were administered parenterally to immunodeficient mice bearing human tumours derived from a human cancer cell line. Anterior, posterior and lateral radioscans of the body were taken with a gamma scintillation camera at various times from immediately to 65 days after injection. Visual displays of the images were processed by standard computer techniques. The model used a human colon-cancer cell line, HT29, an… Show more
“…An inverse relationship between tumour size and antibody uptake has been reported (Moshakis et al, 1981). Nonspecific antibody uptake varied directly with the tumour size but was reduced by necrosis (Epenetos et al, 1982). There may be some unidentified factors presumably related to biological differences in tumour vascularity and or necrosis.…”
The effects of 131-labelled antiferritin polyclonal antibody for the treatment of established hepatocellular carcinoma (HC-04) in athymic nude mice were evaluated. 131I-labelled antiferritin antibody localised specifically to a subcutaneous tumour with a mean of 8.1% of the infused dose per gram of tumour at 24 h after infusion when the experiment was started 15 days after inoculation and with a mean of about 6.5% of the infused dose per gram of tumour when the experiment was started 30 days after tumour transplantation. The concentrations of 131I-antiferritin antibody in tumour delivered a mean of 1994 cGy to tumour following infusion of 500 microCi of radiolabelled antiferritin antibody in the early group and a mean of 1600 cGy in the late group. Treatment with 500 microCi led to regression of the tumour in 55% of animals in the early group and 44% in the late group. In contrast, unlabelled antiferritin and 131I-labelled IgG failed to exert any significant effect on tumour growth. The transplanted tumours in the early groups of animals had relatively higher concentration of ferritin than those in the late group. There was accelerated inhibition of tumour growth and prolonged survival in animals in the early group compared with those in the late group.
“…An inverse relationship between tumour size and antibody uptake has been reported (Moshakis et al, 1981). Nonspecific antibody uptake varied directly with the tumour size but was reduced by necrosis (Epenetos et al, 1982). There may be some unidentified factors presumably related to biological differences in tumour vascularity and or necrosis.…”
The effects of 131-labelled antiferritin polyclonal antibody for the treatment of established hepatocellular carcinoma (HC-04) in athymic nude mice were evaluated. 131I-labelled antiferritin antibody localised specifically to a subcutaneous tumour with a mean of 8.1% of the infused dose per gram of tumour at 24 h after infusion when the experiment was started 15 days after inoculation and with a mean of about 6.5% of the infused dose per gram of tumour when the experiment was started 30 days after tumour transplantation. The concentrations of 131I-antiferritin antibody in tumour delivered a mean of 1994 cGy to tumour following infusion of 500 microCi of radiolabelled antiferritin antibody in the early group and a mean of 1600 cGy in the late group. Treatment with 500 microCi led to regression of the tumour in 55% of animals in the early group and 44% in the late group. In contrast, unlabelled antiferritin and 131I-labelled IgG failed to exert any significant effect on tumour growth. The transplanted tumours in the early groups of animals had relatively higher concentration of ferritin than those in the late group. There was accelerated inhibition of tumour growth and prolonged survival in animals in the early group compared with those in the late group.
“…AUA1 is a murine IgG1 mAb that binds to an antigen expressed by a wide range of adenocarcinoma, including the majority (>90%) of carcinomas of the ovary. The antigen is a 40 kDa glycoprotein (Epenetos et al, 1982). AUA1 has been used in one clinical study (Epenetos et al, 1987).…”
“…A UAI: This mouse IgGi is directed against an epithelial surface antigen found on some normal epithelia, for example in the colon as well as a wide range of carcinomas including those of colon, breast, bronchus and ovary (Epenetos et al, 1982b).…”
This new method of treatment for recurrent malignant effusions is non-toxic and effective resulting in improved quality of life, and, in some cases, prolongation of survival.
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