Stribbling S M, Martin J, Pedley R B, Boden J A, Sharma S K, Springer C J
CRC Centre for Cancer Therapeutics, Institute of Cancer Research, Sutton, Surrey, UK.
Cancer Chemother Pharmacol. 1997;40(4):277-84. doi: 10.1007/s002800050659.
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.
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。