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携带人结肠腺癌异种移植瘤的裸鼠体内用于抗体导向酶前药疗法的抗体-酶偶联物的生物分布

Biodistribution of an antibody-enzyme conjugate for antibody-directed enzyme prodrug therapy in nude mice bearing a human colon adenocarcinoma xenograft.

作者信息

Stribbling S M, Martin J, Pedley R B, Boden J A, Sharma S K, Springer C J

机构信息

CRC Centre for Cancer Therapeutics, Institute of Cancer Research, Sutton, Surrey, UK.

出版信息

Cancer Chemother Pharmacol. 1997;40(4):277-84. doi: 10.1007/s002800050659.

Abstract

The enzyme carboxypeptidase G2 (CPG2) can be targeted to tumors by antibodies and used to activate prodrugs in a treatment called antibody-directed enzyme prodrug therapy (ADEPT). Different doses of CPG2 conjugated to the anti-CEA antibody A5B7 were administered i.v. to nude mice bearing the LS174T human colon adenocarcinoma xenograft, and the biodistribution of conjugate activity 48 and 72 h later was determined using a novel high-performance liquid chromatography (HPLC) method. Conjugate doses of 2,500 and 625 U/kg gave tumor enzyme levels of 0.5-0.6 U/g. Lower doses of 300 and 150 U/kg gave tumor enzyme levels of 0.1-0.3 U/g. Intriguingly, the best tumor:blood ratio of conjugate activity at both 48 and 72 h was achieved after administration of the 625-U/kg dose, not the 2,500-U/kg dose. After 48 h this ratio was 3.8, whereas after 72 h the value was 5.5. This conjugate dose also gave the greatest tumor:tissue ratios in all other tissues examined. After 72 h the tumor:colon ratio was 105, whereas the tumor:kidney ratio was 36. In ADEPT, to obtain maximal tumor damage to LS174T xenografts in nude mice with minimal systemic toxicity using the A5B7-CPG2 conjugate, prodrug should therefore be administered at least 72 h after a conjugate dose of 625 U/kg.

摘要

羧肽酶G2(CPG2)这种酶可以通过抗体靶向肿瘤,并用于在一种称为抗体导向酶前药疗法(ADEPT)的治疗中激活前药。将与抗癌胚抗原(CEA)抗体A5B7偶联的不同剂量的CPG2静脉注射给携带LS174T人结肠腺癌异种移植瘤的裸鼠,并使用一种新型高效液相色谱(HPLC)方法测定48小时和72小时后偶联物活性的生物分布。2500和625 U/kg的偶联物剂量使肿瘤酶水平达到0.5 - 0.6 U/g。300和150 U/kg的较低剂量使肿瘤酶水平达到0.1 - 0.3 U/g。有趣的是,在48小时和72小时时,625 - U/kg剂量给药后实现了最佳的肿瘤与血液的偶联物活性比,而不是2500 - U/kg剂量。48小时后该比例为3.8,而72小时后该值为5.5。该偶联物剂量在所有其他检测组织中也给出了最大的肿瘤与组织比。72小时后,肿瘤与结肠的比例为105,而肿瘤与肾脏的比例为36。因此,在ADEPT中,为了使用A5B7 - CPG2偶联物在裸鼠中对LS174T异种移植瘤造成最大的肿瘤损伤并使全身毒性最小,前药应在625 U/kg偶联物剂量给药后至少72小时给药。

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