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首页> 外文期刊>Protein engineering design & selection: PEDS >A series of anti-CEA/anti-DOTA bispecific antibody formats evaluated for pre-targeting: comparison of tumor uptake and blood clearance
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A series of anti-CEA/anti-DOTA bispecific antibody formats evaluated for pre-targeting: comparison of tumor uptake and blood clearance

机译:评估了针对预靶向的一系列抗CEA /抗DOTA双特异性抗体形式:肿瘤吸收和血液清除的比较

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摘要

A series of anti-tumor/anti-chelate bispecific antibody formats were developed for pre-targeted radioimmunotherapy. Based on the anti- carcinoembryonic antigen humanized hT84.66-M5A monoclonal antibody and the anti-DOTA C8.2.5 scFv antibody fragment, this cognate series of bispecific antibodies were radioiodinated to determine their tumor targeting, biodistribution and pharmacokinetic properties in a mouse xenograft tumor model. The in vivo biodistribution studies showed that all the bispecific antibodies exhibited specific high tumor uptake but the tumor targeting was approximately one-half of the parental anti-CEA mAb due to faster blood clearance. Serum stability and FcRn studies showed no apparent reason for the faster blood clearance. A dual radiolabel biodistribution study revealed that the 111In-DOTA bispecific antibody had increased liver and spleen uptake, not seen for the 125I-version due to metabolism and release of the radioiodine from the cells. These data suggest increased clearance of the antibody fusion formats by the mononuclear phagocyte system. Importantly, a pre-targeted study showed specific tumor uptake of 177Lu-DOTA and a tumor: blood ratio of 199: 1. This pre-targeted radiotherapeutic and substantial reduction in the radioactive exposure to the bone marrow should enhance the therapeutic potential of RIT.
机译:开发了一系列抗肿瘤/抗螯合双特异性抗体形式用于预靶向放射免疫疗法。基于抗癌胚抗原人源化hT84.66-M5A单克隆抗体和抗DOTA C8.2.5 scFv抗体片段,对该同源双系列双特异性抗体进行放射性碘标记,以确定其在小鼠异种移植肿瘤中的肿瘤靶向性,生物分布和药代动力学特性模型。体内生物分布研究表明,所有双特异性抗体均表现出特定的高肿瘤吸收率,但由于更快的血液清除,肿瘤靶向约为亲本抗CEA mAb的一半。血清稳定性和FcRn研究表明,血液清除速度更快没有明显的原因。一项双重放射性标记生物分布研究表明,111In-DOTA双特异性抗体具有增加的肝脏和脾脏摄取,由于放射性碘的代谢和从细胞中释放出来,因此125I-version并未见到。这些数据表明单核吞噬细胞系统对抗体融合形式的清除增加。重要的是,一项预先针对性的研究表明,特定的肿瘤摄取量为177Lu-DOTA,肿瘤与血液的比率为199:1。这种预先针对性的放射治疗和对骨髓的放射暴露的显着减少将增强RIT的治疗潜力。

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