体外和体内随机偶联抗体片段-酶偶联物与位点特异性偶联物的比较。

R C Werlen, R E Offord, D C Blakey, S J East, R G Melton, K Rose
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引用次数: 0

摘要

两种抗体片段-酶偶联物,一种是通过两种蛋白质组分的随机偶联获得的,另一种是通过同一组分的位点特异性连接获得的,在体外和体内比较了它们在抗体定向酶前药物治疗(ADEPT)中的有效性。体外研究表明,位点特异性偶联物具有更高的抗原结合能力,而两种偶联物具有相似的特异性酶活性。在体内,位点特异性偶联物被更快地清除。当对这种更快的清除进行校正时,两种缀合物在给药前在小鼠异种移植系统中显示出相似的抗肿瘤功效。
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In vitro and in vivo comparison of a randomly coupled antibody fragment-enzyme conjugate with a site-specific conjugate.

Two antibody fragment-enzyme conjugates, one obtained by random coupling of the two protein component, the other by site-specific ligation of the same component, were compared in vitro and in vivo for their usefulness in antibody directed enzyme prodrug therapy (ADEPT). The in vitro studies have shown that the site-specific conjugate has a higher antigen binding capacity, while both conjugates had similar specific enzymic activities. In vivo, the site-specific conjugate was cleared more rapidly. When correction was made for this faster clearance, both conjugates showed similar antitumor efficacy in a mouse xenograft system upon administration of a prodrug.

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