Chinn Paul C, Morena Ron A, Santoro Denise A, Kazules Timothy, Kashmiri Syed V S, Schlom Jeffrey, Hanna Nabil, Braslawsky Gary
Biogen Idec, Cambridge, MA, USA.
Cancer Biother Radiopharm. 2006 Apr;21(2):106-16. doi: 10.1089/cbr.2006.21.106.
The primary limitation of IgG antibodies for radioimmunotherapy of solid tumors is their prolonged serum half-life, leading to dose-limiting bone marrow toxicity at doses providing inadequate radiation to the tumor. A humanized C(H)2 domain-deleted variant of the anti-TAG-72 antibody CC49 (HuCC49DeltaC(H)2) has faster blood clearance, compared to the IgG, while retaining tumor targeting. We compared the pharmacokinetics and tumor uptake of (111)In-HuCC49DeltaC(H)2 in BALB/c mice and a colon carcinoma (LS-174T) mouse xenograft with that of (111)In-labeled chimeric CC49 (cCC49), an antibody with pharmacokinetics similar to the humanized CC49 parent. Immuno-conjugates of HuCC49DeltaC(H)2 and cCC49 prepared with the (111)In chelator Mx-DTPA (1-isothiocyantobenzyl-3-methyldiethylenetriaminepentaacetic acid) retained low nM affinity and radiolabeling protocols provided greater than 95% radio-incorporation with (111)In while retaining greater than 80% immunoreactivity. Blood clearance of (111)In-HuCC49DeltaC(H)2 in BALB/c mice was monoexponential (t(1/2) 5.4 hours) and faster than (111)In-cCC49 (biexponential clearance; t1/2Delta 1.5 hours; t1/2beta 162 hours). The (111)In-HuCC49DeltaC(H)2 also cleared more rapidly from the blood in the murine xenograft. At 1 hour postinjection, blood concentrations for (111)In-HuCC49DeltaC(H)2 and (111)In-cCC49 were comparable (25.5 injected dose per g [%ID/g] and 21.3 %ID/g, respectively); tumor uptake for (111)In- HuCC49DeltaC(H)2 was 7.9 %ID/g, compared to 7.5 %ID/g for (111)In-cCC49. However, at 24 hours, blood concentration for (111)In-HuCC49DeltaC(H)2 was less than (111)In-cCC49 (0.9 %ID/g versus 5.2 %ID/g, respectively) with comparable tumor retention (14.4 %ID/g versus 19.0 %ID/g, respectively). Faster blood clearance of (111)In-HuCC49DeltaC(H)2 and tumor localization comparable to that of (111)In-cCC49 provided a fourfold improved tumor-to-blood ratio for (111)In-HuCC49DeltaC(H)2 at 24 hours postinjection.
IgG抗体用于实体瘤放射免疫治疗的主要局限性在于其血清半衰期延长,在给予肿瘤的辐射剂量不足时会导致剂量限制性骨髓毒性。与IgG相比,抗TAG-72抗体CC49的人源化C(H)2结构域缺失变体(HuCC49DeltaC(H)2)具有更快的血液清除率,同时保留肿瘤靶向性。我们比较了(111)In-HuCC49DeltaC(H)2在BALB/c小鼠和结肠癌(LS-174T)小鼠异种移植模型中的药代动力学和肿瘤摄取情况,以及(111)In标记的嵌合CC49(cCC49)的药代动力学和肿瘤摄取情况,cCC49是一种药代动力学与人源化CC49亲本相似的抗体。用(111)In螯合剂Mx-DTPA(1-异硫氰酸苄基-3-甲基二乙三胺五乙酸)制备的HuCC49DeltaC(H)2和cCC49免疫偶联物保留了低纳摩尔亲和力,放射性标记方案使(111)In的放射性掺入率大于95%,同时保留了大于80%的免疫反应性。(111)In-HuCC49DeltaC(H)2在BALB/c小鼠中的血液清除呈单指数形式(t(1/2) 5.4小时),比(111)In-cCC49更快(双指数清除;t1/2Delta 1.5小时;t1/2beta 162小时)。(111)In-HuCC49DeltaC(H)2在小鼠异种移植模型中也从血液中清除得更快。注射后1小时,(111)In-HuCC49DeltaC(H)2和(111)In-cCC49的血液浓度相当(分别为每克注射剂量的25.5 [%ID/g]和21.3 %ID/g);(111)In-HuCC49DeltaC(H)2的肿瘤摄取为7.9 %ID/g,而(111)In-cCC49为7.5 %ID/g。然而,在24小时时,(111)In-HuCC49DeltaC(H)2的血液浓度低于(111)In-cCC49(分别为0.9 %ID/g和5.2 %ID/g),肿瘤滞留情况相当(分别为14.4 %ID/g和19.0 %ID/g)。(111)In-HuCC49DeltaC(H)2更快的血液清除率以及与(111)In-cCC49相当的肿瘤定位,使得注射后24小时(111)In-HuCC49DeltaC(H)2的肿瘤与血液比值提高了四倍。