Center for Radiopharmaceutical Sciences ETH-PSI-USZ, Paul Scherrer Institute, Villigen, Switzerland.
PLoS One. 2013;8(4):e60350. doi: 10.1371/journal.pone.0060350. Epub 2013 Apr 2.
Site-specific enzymatic reactions with microbial transglutaminase (mTGase) lead to a homogenous species of immunoconjugates with a defined ligand/antibody ratio. In the present study, we have investigated the influence of different numbers of 1,4,7,10-tetraazacyclododecane-N-N'-N''-N'''-tetraacetic acid (DOTA) chelats coupled to a decalysine backbone on the in vivo behavior of the chimeric monoclonal anti-L1CAM antibody chCE7agl. The enzymatic conjugation of (DOTA)1-decalysine, (DOTA)3-decalysine or (DOTA)5-decalysine to the antibody heavy chain (via Gln295/297) gave rise to immunoconjugates containing two, six or ten DOTA moieties respectively. Radiolabeling of the immunoconjugates with (177)Lu yielded specific activities of approximately 70 MBq/mg, 400 MBq/mg and 700 MBq/mg with increasing numbers of DOTA chelates. Biodistribution experiments in SKOV3ip human ovarian cancer cell xenografts demonstrated a high and specific accumulation of radioactivity at the tumor site for all antibody derivatives with a maximal tumor accumulation of 43.6±4.3% ID/g at 24 h for chCE7agl-[(DOTA)-decalysine]2, 30.6±12.0% ID/g at 24 h for chCE7agl-[(DOTA)3-decalysine]2 and 49.9±3.1% ID/g at 48 h for chCE7agl-[(DOTA)5-decalysine)]2. The rapid elimination from the blood of chCE7agl-[(DOTA)-decalysine]2 (1.0±0.1% ID/g at 24 h) is associated with a high liver accumulation (23.2±4.6% ID/g at 24 h). This behavior changed depending on the numbers of DOTA moieties coupled to the decalysine peptide with a slower blood clearance (5.1±1.0 (DOTA)3 versus 11.7±1.4% ID/g (DOTA)5, p<0.005 at 24 h) and lower radioactivity levels in the liver (21.4±3.4 (DOTA)3 versus 5.8±0.7 (DOTA)5, p<0.005 at 24 h). We conclude that the site-specific and stoichiometric uniform conjugation of the highly DOTA-substituted decalysine ((DOTA)5-decalysine) to an anti-tumor antibody leads to the formation of immunoconjugates with high specific activity and excellent in vivo behavior and is a valuable option for radioimmunotherapy and potentially antibody-drug conjugates (ADCs).
利用微生物转谷氨酰胺酶(mTGase)进行的特异性酶反应导致具有定义的配体/抗体比的同种类免疫缀合物。在本研究中,我们研究了不同数量的 1,4,7,10-四氮杂环十二烷-N-N'-N''-N'''-四乙酸(DOTA)螯合物偶联到 decalysine 骨架上对嵌合单克隆抗 L1CAM 抗体 chCE7agl 的体内行为的影响。通过 Gln295/297 将(DOTA)1-decalysine、(DOTA)3-decalysine 或(DOTA)5-decalysine 酶促偶联到抗体重链上,分别得到含有两个、六个或十个 DOTA 部分的免疫缀合物。用(177)Lu 标记免疫缀合物,得到约 70 MBq/mg、400 MBq/mg 和 700 MBq/mg 的放射性比活度,DOTA 螯合物的数量增加。在 SKOV3ip 人卵巢癌细胞异种移植的体内分布实验中,所有抗体衍生物均在肿瘤部位表现出高特异性放射性累积,在 24 小时时 chCE7agl-[(DOTA)-decalysine]2 的最大肿瘤累积为 43.6±4.3%ID/g,chCE7agl-[(DOTA)3-decalysine]2 为 30.6±12.0%ID/g,chCE7agl-[(DOTA)5-decalysine)]2 为 49.9±3.1%ID/g。chCE7agl-[(DOTA)-decalysine]2 的快速从血液中清除(24 小时时为 1.0±0.1%ID/g)与肝脏的高累积有关(24 小时时为 23.2±4.6%ID/g)。这种行为取决于偶联到 decalysine 肽上的 DOTA 部分的数量,随着血液清除速度的减慢(24 小时时为 5.1±1.0(DOTA)3 与 11.7±1.4%ID/g(DOTA)5,p<0.005)和肝脏中放射性水平降低(24 小时时为 21.4±3.4(DOTA)3 与 5.8±0.7(DOTA)5,p<0.005)。我们得出结论,高度 DOTA 取代的 decalysine((DOTA)5-decalysine)与肿瘤抗体的位点特异性和化学计量均匀缀合导致形成具有高比活度和优异体内行为的免疫缀合物,是放射免疫治疗和潜在抗体药物偶联物(ADC)的有价值选择。