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抗体蛋白剂量对放射性抗体肿瘤分布均匀性的影响:一项放射自显影研究。

The effect of antibody protein dose on the uniformity of tumor distribution of radioantibodies: an autoradiographic study.

作者信息

Blumenthal R D, Fand I, Sharkey R M, Boerman O C, Kashi R, Goldenberg D M

机构信息

Garden State Cancer Center, Newark, NJ 07103.

出版信息

Cancer Immunol Immunother. 1991;33(6):351-8. doi: 10.1007/BF01741594.

Abstract

The inaccessibility of radiolabeled antibody to poorly vascularized regions of solid tumors may reduce the therapeutic efficacy of these macromolecules. Theoretical mathematical models have predicted that increasing the protein dose administered would reduce the heterogeneity of radioantibody distribution. This investigation was undertaken to evaluate this hypothesis in experimental animal models. We have utilized the technique of macroautoradiography to demonstrate an increase in tumor penetration of the lower-affinity 125I-labeled NP-4 or higher-affinity Immu-14 anti-carcinoembryonic antigen (anti-CEA) mAbs into small (60.25-0.4 g) and large (0.8-1.5 g) GW-39 and LS174T human colonic xenografts, grown subcutaneously in the nude mouse, when 400 micrograms unlabeled antibody is administered simultaneously with 10 micrograms (100 microCi) radioantibody. Further increases in protein to 800 micrograms result in a reduction in total tumor uptake of the antibody. These in a reduction in total tumor uptake of the antibody. These differences in mAb distribution could be visualized as early as 1 day after antibody injection. Improved mAb penetration was also achieved for the Mu-9 anti-CSAp (anti-mucin) antibody using 800 micrograms unlabeled antibody. An irrelevant antibody (AFP-7-31) was found to be homogeneously distributed 3 days after injection, even at a low protein dose. Attempts to improve mAb penetration by increasing the protein dose in the GS-2 colorectal tumor, a model that has low NP-4 accretion as a result physiological barriers separating antibody from antigen, were not successful. These results suggest that a more homogeneous distribution of radioantibody can be achieved by carefully selecting a dose of unlabeled antibody to coadminister. Work is currently in progress to determine the effect of improved tumor distribution of radioantibody on the therapeutic potential of a single dose of radioantibody.

摘要

放射性标记抗体难以进入实体瘤血管化不良的区域,这可能会降低这些大分子的治疗效果。理论数学模型预测,增加蛋白质给药剂量会降低放射性抗体分布的异质性。本研究旨在在实验动物模型中评估这一假设。我们利用宏观放射自显影技术证明,当同时给予400微克未标记抗体和10微克(100微居里)放射性抗体时,低亲和力的125I标记NP-4或高亲和力的Immu-14抗癌胚抗原(抗CEA)单克隆抗体在裸鼠皮下生长的小(60.25 - 0.4克)和大(0.8 - 1.5克)GW-39和LS174T人结肠异种移植瘤中的肿瘤穿透性增加。蛋白质剂量进一步增加至800微克会导致抗体在肿瘤中的总摄取量减少。这些抗体摄取量的差异在抗体注射后1天即可观察到。使用800微克未标记抗体时,Mu-9抗CSAp(抗粘蛋白)抗体的穿透性也得到了改善。发现一种无关抗体(AFP-7-31)在注射后3天均匀分布,即使蛋白质剂量很低。在GS-2结肠肿瘤模型中,由于生理屏障使抗体与抗原分离,导致NP-4积聚较低,试图通过增加蛋白质剂量来提高单克隆抗体的穿透性未成功。这些结果表明,通过仔细选择共同给药的未标记抗体剂量,可以实现放射性抗体更均匀的分布。目前正在进行研究,以确定改善放射性抗体在肿瘤中的分布对单剂量放射性抗体治疗潜力的影响。

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