Koros A M, Tobin M J, Epperly M W, Levine G, McGinley J R
Department of Infectious Diseases and Microbiology, Graduate School Public Health, University of Pittsburgh, Pennsylvania.
Anticancer Res. 1993 Nov-Dec;13(6A):1953-6.
A model is described by which in vivo tumor-MOAB interactions may be investigated. The method is rapid and may aid in the selection of appropriate MOABS from a panel of MOABS for individualized patient treatment. Groups of athymic nude mice were injected intravenously with small cell lung cancer line SHP-77 cells which are trapped primarily in the lungs. Twenty-four hours post tumor cell inoculation, 186Rhenium tagged HNK1 MOAB (CD57) was injected intravenously. Controls which received no tumor cells were injected with unbound 186Re or radioactive MOAB. Biodistribution studies at 24 hours following MOAB injection showed significantly more radioactivity in lungs of mice inoculated with both SHP-77 cells and 186Re MOAB than did lungs of controls.
本文描述了一种可用于研究体内肿瘤与单克隆抗体(MOAB)相互作用的模型。该方法快速,有助于从一组单克隆抗体中选择合适的单克隆抗体用于个体化患者治疗。将无胸腺裸鼠分组,经静脉注射主要滞留在肺部的小细胞肺癌细胞系SHP-77细胞。肿瘤细胞接种后24小时,经静脉注射铼-186标记的HNK1单克隆抗体(CD57)。未接种肿瘤细胞的对照组注射未结合的铼-186或放射性单克隆抗体。单克隆抗体注射后24小时的生物分布研究表明,接种SHP-77细胞和铼-186单克隆抗体的小鼠肺部放射性明显高于对照组小鼠肺部。