Shah S A, Gallagher B M, Sands H
J Natl Cancer Inst. 1987 Jun;78(6):1069-77.
The potential of radioiodinated monoclonal antibody B72.3 for lymphoscintigraphy was evaluated, using suitable animal models of a human colorectal carcinoma. LS174T xenografts were grown at various sites in beta-estradiol-pretreated athymic mice, and the development of metastases in different organs was assessed histologically. After iv inoculation of the mice, 66% of the animals developed "metastases" to the axillary lymph nodes. Of these mice, 100% also developed multiple tumors on their backs and 79% had lung micrometastases. Livers, kidneys, and spleens showed no evidence of tumor growth. In 33% of the mice in which primary LS174T tumors had been removed from the hindfoot pad, metastases to the popliteal lymph nodes were observed 3 1/2 weeks after tumor implantation. BALB/c (nu/nu) female mice bearing axillary and popliteal lymph node metastases were used to test the potential of radiolabeled B72.3 antibody (an IgG1) as a lymphoscintigraphic agent. A monoclonal antibody against horseradish peroxidase (also an IgG1), which did not bind LS174T tumor cells in vitro, served as a control. Both normal and tumor-bearing axillary and popliteal lymph nodes imaged up to 6 hours after the sc injection of 20-40 mu Ci of 125I-labeled B72.3 into either the forefoot or hindfoot pads. The localization index (L.I.) (specific/nonspecific antibody in tumor divided by specific/nonspecific antibody in blood) for LS174T tumors in lymph nodes was approximately 1 during the first 6 hours after antibody injection, thus indicating no specific antibody accumulation. Twenty-four hours and later after sc injection, images of nodal metastases (14-477 mg) and specific antibody accumulations were observed. At these times the L.I.'s ranged 1.5-3.5. Tumor-negative nodes did not image at 24 hours after injection of 125I-labeled B72.3. The L.I.'s of the normal nodes and of other tissues from these mice were about 1.0 at 24 hours, indicating no specific antibody accumulation. Autoradiographic analysis of lymph nodes containing LS174T tumor showed heterogeneous antibody distribution of B72.3 within tumor sections with heavy patches of antibody accumulation in mucin globules. In lymph nodes the normal lymphocytes adjacent to the LS174T tumor cells showed no antibody accumulation. The lack of specific, early antibody accumulation by LS174T tumor-bearing nodes in mice suggests that B72.3 does not accumulate in nodal metastases to the degree necessary to consider it a potential agent for use in lymphoscintigraphy.
利用合适的人结肠直肠癌动物模型,对放射性碘化单克隆抗体B72.3用于淋巴闪烁造影的潜力进行了评估。将LS174T异种移植物接种于经β-雌二醇预处理的无胸腺小鼠的不同部位,并通过组织学方法评估不同器官中转移灶的形成情况。给小鼠静脉接种后,66%的动物出现腋窝淋巴结“转移”。在这些小鼠中,100%的小鼠背部还出现了多个肿瘤,79%的小鼠有肺微转移。肝脏、肾脏和脾脏未显示肿瘤生长迹象。在33%的后足垫原发性LS174T肿瘤已被切除的小鼠中,肿瘤植入后3.5周观察到腘窝淋巴结转移。携带腋窝和腘窝淋巴结转移灶的BALB/c(nu/nu)雌性小鼠被用于测试放射性标记的B72.3抗体(一种IgG1)作为淋巴闪烁造影剂的潜力。一种抗辣根过氧化物酶的单克隆抗体(也是一种IgG1),在体外不与LS174T肿瘤细胞结合,用作对照。在前足垫或后足垫皮下注射20 - 40μCi的125I标记的B72.3后,正常和荷瘤的腋窝及腘窝淋巴结在长达6小时内均显影。抗体注射后的最初6小时内,LS174T肿瘤在淋巴结中的定位指数(L.I.)(肿瘤中特异性/非特异性抗体除以血液中特异性/非特异性抗体)约为1,这表明没有特异性抗体蓄积。皮下注射24小时及之后,观察到淋巴结转移灶(14 - 477mg)的图像和特异性抗体蓄积。此时L.I.范围为1.5 - 3.5。注射125I标记的B72.3后24小时,肿瘤阴性的淋巴结未显影。这些小鼠正常淋巴结和其他组织的L.I.在24小时时约为1.0,表明没有特异性抗体蓄积。对含有LS174T肿瘤的淋巴结进行放射自显影分析显示,B72.3在肿瘤切片内的抗体分布不均匀,在粘蛋白小球中有大量抗体蓄积。在淋巴结中,与LS174T肿瘤细胞相邻的正常淋巴细胞未显示抗体蓄积。荷LS174T肿瘤小鼠的淋巴结缺乏特异性早期抗体蓄积,这表明B72.3在淋巴结转移灶中的蓄积程度不足以使其被视为淋巴闪烁造影的潜在药物。