De Santis Rita, Albertoni Claudio, Petronzelli Fiorella, Campo Silvia, D'Alessio Valeria, Rosi Antonio, Anastasi Anna Maria, Lindstedt Ragnar, Caroni Nadia, Arseni Brunilde, Chiodi Pierino, Verdoliva Antonio, Cassani Giovanni, Chinol Marco, Paganelli Giovanni, Carminati Paolo
Sigma-Tau SpA, R&D, Rome, Italy.
Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):2191-6. doi: 10.1158/1078-0432.CCR-05-2526.
ST2146biot is a biotinylated anti-tenascin monoclonal antibody (mAb) to be used for Pretargeted Antibody Guided Radioimmunotherapy (PAGRIT) of solid tumors. In vivo biodistribution studies of (125)I-labeled ST2146biot were done in nude mice transplanted with human HT-29 colon carcinoma and/or human U-118MG glioblastoma cells characterized for low and high tenascin expression, respectively. In vitro results show that ST2146 retains immunoreactivity upon biotinylation, in contrast to other anti-tenascin mAbs. In vivo biodistribution of ST2146 shows specific tumor accumulation up to 10 days after the i.v. injection, with no relevant differences between biotinylated and nonbiotinylated ST2146. A dose of 4 microg/mouse saturates the low tenascin-expressing human colon carcinoma HT-29, whereas the high tenascin-expressing human glioblastoma U-118MG seems to be saturated at a ST2146biot dose between 320 and 640 microg/mouse. The percentage of injected dose per gram of tumor ranges from 10% to 30%, corresponding to an amount of ST2146biot/g of tumor of approximately 400 ng/g and >200 microg/g for HT-29 and U-118MG, respectively. Tumor to normal organs uptake ratios are between 15 and 60, confirming high tumor selectivity of ST2146biot despite its cross-reactivity with the tenascin expressed at low level in the normal mouse organs. The ST2146biot localization data are substantially confirmed even when both low and high tenascin-expressing tumors are implanted in the same animal. To our knowledge, the absolute amount of ST2146biot, specifically localized in xenotransplanted human tumors, is the highest thus far described and supports the clinical use of this mAb in PAGRIT(R).
ST2146biot是一种生物素化抗腱生蛋白单克隆抗体(mAb),用于实体瘤的预靶向抗体引导放射免疫疗法(PAGRIT)。对用分别具有低和高腱生蛋白表达特征的人HT-29结肠癌和/或人U-118MG胶质母细胞瘤细胞移植的裸鼠进行了(125)I标记的ST2146biot的体内生物分布研究。体外结果表明,与其他抗腱生蛋白单克隆抗体相比,ST2146在生物素化后仍保留免疫反应性。ST2146的体内生物分布显示,静脉注射后长达10天肿瘤有特异性聚集,生物素化和未生物素化的ST2146之间无相关差异。4微克/只小鼠的剂量可使低表达腱生蛋白的人结肠癌HT-29饱和,而高表达腱生蛋白的人胶质母细胞瘤U-118MG似乎在320至640微克/只小鼠的ST2146biot剂量下饱和。每克肿瘤注射剂量的百分比范围为10%至30%,分别对应于HT-29和U-118MG每克肿瘤中约400纳克/克和>200微克/克的ST2146biot量。肿瘤与正常器官的摄取比率在15至60之间,证实了ST2146biot具有高肿瘤选择性,尽管它与正常小鼠器官中低水平表达的腱生蛋白有交叉反应。即使在同一只动物中植入低表达和高表达腱生蛋白的肿瘤,ST2146biot的定位数据也得到了充分证实。据我们所知,特异性定位于异种移植人肿瘤中的ST2146biot的绝对量是迄今为止报道的最高值,并支持该单克隆抗体在PAGRIT(R)中的临床应用。