Blumenthal R D, Kashi R, Stephens R, Sharkey R M, Goldenberg D M
Center for Molecular Medicine and Immunology, Neward, N.J. 07103.
Cancer Immunol Immunother. 1991;32(5):303-10. doi: 10.1007/BF01789048.
Radioimmunotherapy of GW-39 human colonic tumor xenografts grown in the hamster cheek pouch with 131I-labeled NP-4 anti-(carcinoembryonic antigen) (CEA) and 131I-labeled Mu-9 anti-(color-specific antigen-p) (CSAp) murine monoclonal antibodies, administered in combination, was more effective than using either antibody alone for tumor masses less than 0.5 cm3 in size. The antibody mixture had no therapeutic advantage for larger tumors. Therapeutic efficacy was determined by measuring the change in tumor size over time, quantifying the absolute number of tumors responding to radioantibody therapy, and determining the percentage growth inhibition of each treatment at various times after radioantibody administration. Several mechanisms are discussed to explain the improved tumoricidal effect of the antibody mixture noted in this model system, such as (a) the possibility that an antibody mixture could target a greater number of tumor cells, (b) the potential for antibody mixtures to provide better tumor distribution and (c) the possibility that antibodies administered in combination can increase the magnitude of tumor uptake of individual radioantibodies, thereby resulting in a greater radiation dose delivered to the tumor.
用131I标记的NP-4抗(癌胚抗原)(CEA)和131I标记的Mu-9抗(颜色特异性抗原-p)(CSAp)鼠单克隆抗体联合对生长在仓鼠颊囊中的GW-39人结肠肿瘤异种移植物进行放射免疫治疗,对于体积小于0.5 cm3的肿瘤块,联合使用比单独使用任何一种抗体更有效。对于较大的肿瘤,抗体混合物没有治疗优势。通过测量肿瘤大小随时间的变化、量化对放射抗体治疗有反应的肿瘤的绝对数量以及确定放射抗体给药后不同时间每种治疗的生长抑制百分比来确定治疗效果。讨论了几种机制来解释在该模型系统中观察到的抗体混合物增强的杀肿瘤作用,例如:(a)抗体混合物可能靶向更多肿瘤细胞的可能性;(b)抗体混合物可能提供更好的肿瘤分布的可能性;(c)联合给药的抗体可能增加单个放射抗体在肿瘤中的摄取量,从而导致传递到肿瘤的辐射剂量更大的可能性。