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Preclinical Evaluation of SPECT Imaging with 131 ∣–Labeled Monoclonal Antibody SZ39 in Nude Mice Bearing Human Glioma Xenografts
Author(s) -
Lan Qing,
Huang Qiang,
Bao Shiyao
Publication year - 1996
Publication title -
journal of neuroimaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.822
H-Index - 64
eISSN - 1552-6569
pISSN - 1051-2284
DOI - 10.1111/jon199662131
Subject(s) - medicine , monoclonal antibody , glioma , nuclear medicine , pathology , spect imaging , cancer research , antibody , immunology
The imaging characteristics of monoclonal antibody SZ39 against glioma were evaluated in glioma–bearing nude mice. Monoclonal antibody SZ39 is a murine lgG2a that reacts with a glycoprotein epitope (molecular weight 180,000), a human glioma–associated membrane antigen. Monoclonal antibody SZ39 was labeled with 131 ∣using a modified chloramine T method. Each glioma–bearing nude mouse was given 50 µCi/40 µg of the experimental agent, 131 ∣–labeled monoclonal antibody, or 50 µCi/46 µg of a control agent, 131 ∣–labeled monoclonal antibody C50, an antibody against colon cancer. Single–photon emission computed tomography (SPECT) was performed every 24 hours in the first week after administration. Glioma–bearing nude mice were killed in groups of 3 at 24 hours and daily up to 72 hours. The ratio of radioactivity uptake in glioma to normal organs was calculated. After administration of the labeled SZ39, glioma was visualized with SPECT on days 1 to 7, particularly at 72 hours. There was no accumulation of radioactivity in glioma with the labeled C50 antibody. All glioma–organ ratios increased with time. At 72 hours, the ratio of glioma to brain was 22.46 and of the other organs was 2.64 on average. SZ39 had a relatively low endocytosis rate and was favorable for 131 ∣ labeling. These characteristics were helpful to reduce free 131 ∣ in the blood and reduce the uptake by other organs. The results suggest that 131 ∣–labeled SZ39 selectively accumulates in glioma, representing a potential strategy for SPECT imaging of these lesions.