COMBINATIONS OF NONLABELED, I-125 LABELED, AND ANTIIDIOTYPIC ANTIPLACENTAL ALKALINE-PHOSPHATASE MONOCLONAL-ANTIBODIES AT EXPERIMENTAL RADIOIMMUNOTARGETING
Rr. Norrlund et al., COMBINATIONS OF NONLABELED, I-125 LABELED, AND ANTIIDIOTYPIC ANTIPLACENTAL ALKALINE-PHOSPHATASE MONOCLONAL-ANTIBODIES AT EXPERIMENTAL RADIOIMMUNOTARGETING, Acta radiologica, 38(6), 1997, pp. 1087-1093
Purpose: Placental alkaline phosphatase (FLAP) is a membrane-bound onc
ofetal antigen that can be used for radioimmunotargeting. Preinjection
of nonlabeled monoclonal anti-FLAP antibody (H7) and postinjection of
monoclonal anti-idiotypic anti-PLAP antibody (alpha H7) were used in
order to improve the localization efficacy of I-125-labeled H7. Materi
al and Methods: A human cervix adenocarcinoma cell line (HeLa Hep 2) w
as inoculated subcutaneously in 24 nude mice. Repeated quantitative ra
dioimmunoscintigraphic recordings were performed on 27 occasions in ea
ch of the 24 mice during the observation period which lasted for nearl
y 3 months. The tumor and nontumor doses were calculated according to
the Medical International Radiation Dose Committee formula on the basi
s of the scintigraphic data. Results: All tumors were clearly visualiz
ed as early as one day after injection of I-125-labeled H7. The remain
ing radioactivity was exclusively located in the tumors at days 30-81.
As much as 12-16% of the injected dose/g accumulated in the tumors du
ring the first 2 days after injection, and remained stable at this hig
h level for approximately 10 days in all investigated groups. Radioact
ivity in the whole body was rapidly eliminated during the same time pe
riod. The highest tumor/nontumor dose ratio was obtained after a singl
e injection of I-125-labeled H7. Conclusion: Neither a preinjection of
nonlabeled H7 nor a postinjection of alpha H7 nor a combination of bo
th strategies resulted in improved tumor/nontumor dose ratios compared
to a single injection of labeled H7. The monoclonal antibody H7 has a
rapid and high uptake, combined with a prolonged retention time in th
e tumors. The kinetic properties of H7 are different from antibodies t
argeting intracellular tumor antigens.