Walker K Z, Seymour-Munn K, Keech F K, Axiak S M, Bautovich G J, Morris J G, Basten A
Eur J Nucl Med. 1986;12(9):461-7. doi: 10.1007/BF00254751.
A novel experimental model was established in normal rats for studying the localisation and tissue distribution of a murine monoclonal antibody directed against kappa light chain B cell malignancies. The antibody, K-1-21 was raised against human kappa Bence Jones Proteins and reacts with a cell membrane antigen KMA which is restricted to some kappa myeloma and lymphoma cells. In the rat model, kappa or lambda Bence Jones protein-conjugated sepharose was implanted subcutaneously on either flank 24 h before the injection of 131I-labelled K-1-21 or its F(ab')2 fragment. Gamma camera imaging and tissue distribution studies showed specific localisation of the K-1-21 antibody in the kappa sepharose. Injection of F(ab')2 antibody fragments resulted in faster background clearance, earlier delineation of the specific image and significantly higher target to blood ratios than those obtained with the intact antibody. These results suggest that the model may provide an alternative system to tumour xenograft bearing nude mice for studying localisation of antibodies with therapeutic potential.
为研究一种针对κ轻链B细胞恶性肿瘤的鼠单克隆抗体的定位和组织分布,在正常大鼠中建立了一种新型实验模型。该抗体K-1-21是针对人κ本斯·琼斯蛋白产生的,与一种细胞膜抗原KMA反应,该抗原仅限于某些κ骨髓瘤和淋巴瘤细胞。在大鼠模型中,在注射131I标记的K-1-21或其F(ab')2片段前24小时,将κ或λ本斯·琼斯蛋白偶联的琼脂糖皮下植入两侧胁腹。γ相机成像和组织分布研究显示K-1-21抗体在κ琼脂糖中特异性定位。注射F(ab')2抗体片段导致本底清除更快,特异性图像更早显现,且靶血比显著高于完整抗体。这些结果表明,该模型可能为研究具有治疗潜力的抗体定位提供一种替代裸鼠荷瘤异种移植的系统。