Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, USA.
MAbs. 2010 Jan-Feb;2(1):67-72. doi: 10.4161/mabs.2.1.10781. Epub 2010 Jan 26.
Carcinoembryonic antigen (CEA) is a glycosylated cell surface antigen known to be highly overexpressed in several adenocarcinomas, including colorectal cancer, while demonstrating limited expression in normal tissues. Prior work has shown that the plasma clearance of T84.66, a monoclonal anti-CEA antibody, is enhanced by several-fold in a CEA-expressing xenograft mouse model, suggesting the presence of a target mediated elimination pathway. The purpose of this study is to investigate the influence of tumor volume on the plasma clearance of T84.66, and test the hypothesis that the plasma pharmacokinetics of T84.66 may be used as a sensitive and selective test for the diagnosis of CEA-positive tumors. T84.66 plasma pharmacokinetics were studied following intravenous (i.v.) administration of a 1 mg/kg dose in animals without tumor and mice bearing low (20-75 mm(3)), medium (400-570 mm(3)), and high volume (800-1,200 mm(3)) LS174T xenografts. Based on comparison of the disposition of T84.66 in non-tumor bearing mice and mice bearing low-volume tumors, it was predicted that a single plasma concentration of T84.66, obtained seven days after dosing, would provide a sensitive and selective means of determining the presence of tumor in mice. A blinded follow-up study was conducted using athymic mice with or without intraperitoneal LS174T xenografts. 1 mg/kg of (125)I-T84.66 was administered i.v., and plasma samples were collected on day 7. Comparison of the observed concentration of (125)I-T84.66 to the pre-determined threshold value (7.63 nM) enabled identification of tumor bearing mice with a sensitivity of 93.3% and specificity of 100%.
癌胚抗原(CEA)是一种糖基化的细胞表面抗原,已知在包括结直肠癌在内的几种腺癌中高度过表达,而在正常组织中表达有限。先前的工作表明,在表达 CEA 的异种移植小鼠模型中,单克隆抗 CEA 抗体 T84.66 的血浆清除率提高了几倍,这表明存在一种靶向介导的消除途径。本研究旨在探讨肿瘤体积对 T84.66 血浆清除率的影响,并检验 T84.66 的血浆药代动力学可作为诊断 CEA 阳性肿瘤的敏感和选择性检测方法的假设。在无肿瘤和荷低(20-75mm(3))、中(400-570mm(3))和高(800-1200mm(3))LS174T 异种移植瘤的动物中,静脉(i.v.)给予 1mg/kg 剂量后研究了 T84.66 的血浆药代动力学。基于非肿瘤荷瘤小鼠和荷低瘤小鼠 T84.66 分布的比较,预测在给药后 7 天获得的 T84.66 单次血浆浓度将提供一种敏感和选择性的方法来确定小鼠是否存在肿瘤。在有无腹腔 LS174T 异种移植瘤的无胸腺小鼠中进行了一项盲法后续研究。静脉给予 1mg/kg 的 (125)I-T84.66,在第 7 天采集血浆样本。将观察到的 (125)I-T84.66 浓度与预先确定的阈值(7.63nM)进行比较,能够以 93.3%的灵敏度和 100%的特异性识别荷瘤小鼠。