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Localization of radiolabelled F(ab′) 2 fragments of monoclonal antibodies in nude mice bearing intraperitoneally growing human ovarian cancer xenografts
Author(s) -
Moseley Karan R.,
Battaile Anne,
Knapp Robert C.,
Haisma Hidde J.
Publication year - 1988
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910420311
Subject(s) - monoclonal antibody , ovarian cancer , antibody , nude mouse , cancer , ovary , cancer research , ratón , immunohistochemistry , epithelioma , medicine , pathology , biology , immunology , carcinoma
The biodistribution and pharmacokinetics of 2 monoclonal antibodies (MAbs) specific for ovarian carcinoma, OC125 and OV‐TL3, were studied in nude mice bearing intraperitoneally (i. p.) growing human ovarian carcinoma xenografts of NIH:OVCAR‐3. The ovarian carcinoma xenografts grew as non‐adherent cells in ascites and as solid implants in the peritoneal cavity of injected mice. The biodistribution and pharmacokinetics were determined by measurement of radioactivity in tumor masses, ascites, blood and other tissues after intravenous (i. v.) and i. p. injection of radioiodinated F(ab′) 2 fragments of MAbs. The specificity of the observed tumor localization was then evaluated by comparing the uptake of the anti‐ovarian carcinoma antibodies OCI25 and OV‐TL3 with the uptake of a radioiodinated non‐ovarian carcinomaspecific MAb A2C6. The results of the study indicate that uptake of the anti‐ovarian carcinoma antibodies was highest in the non‐adherent tumor cells in the ascites after i. p. injection. The observed uptake was 85% Injected dose/g for OV‐TL3 and 22% injected dose/g for OCI25. This compares to the observed antibody uptake of 9% injected dose/g for OV‐TL3 and less than I% injected dose/g for OCI25 in solid tumor masses after i. p. injection. After i. v. injection, uptake of OCI25 and OV‐TL3 was less than 3% injected dose/g, both for nonadherent tumor cells and for solid tumor masses. The data support the conclusion that OV‐TL3 is superior to OC125 and that i. p. administration of radiolabelled MAb F(ab′) 2 fragments is superior to their i. v. administration for immunotherapy of ovarian carcinoma.