Sabbah Emmanuelle N, Kadouche Jean, Ellison David, Finucane Ciara, Decaudin Didier, Mather Stephen J
M.A.T., Génocampus 1, 5 rue Henri Desbrvères, 91030 Evry cedex, France.
Nucl Med Biol. 2007 Apr;34(3):293-304. doi: 10.1016/j.nucmedbio.2007.01.004.
Pancreatic cancer has a very poor prognosis with a less than 5% survival rate at 5 years. Neither external beam radiation nor chemotherapy, alone or in combination, have given encouraging results so far. A possible solution might come from the use of targeted therapy such as radioimmunotherapy. We present here the results obtained from the preclinical development of a new monoclonal antiferritin antibody (Ab), AMB8LK. Ferritin is overexpressed in pancreatic cancer and could thus be used as a target for the delivery of radioactivity at the tumour sites. The AMB8LK Ab was conjugated to three chelating agents: the 2-(4-isothiocyanatobenzyl)-diethylenetriamine pentaacetic acid (PSCN-Bz-DTPA), the (R)-2-amino-3-(4-isothiocyanatophenyl)propyl]-trans-(S,S)-cyclohexane-1,2-diamine-pentaacetic acid (p5CN-Bz-CHX-A"-DTPA) and the 2-(4-isothiocyanatobenzyl)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (pSCN-Bz-DOTA). Radiolabelling of the three immunoconjugates with indium 111 and yttrium 90 as well as in vitro stability and immunoreactivity against pure ferritin and cells expressing ferritin were analysed. In vivo biodistribution studies were conducted on normal and on human pancreatic adenocarcinoma CAPAN-1 tumour bearing mice. These experiments demonstrated good radiolabelling (>95%), stability and immunoreactivity of the three compounds. In the biodistribution studies, differences between the three immunoconjugates were apparent in the rate of blood clearance and in tumour, liver and bone uptake. A very good pancreatic adenocarcinoma tumour targeting was observed especially with the Bz-DTPA-AMB8LK: 20% of the injected dose of the indium-labelled compound 3 days after injection; 15% of the injected dose 5 days after that of the yttrium-labelled Ab. Altogether, these results in animal models suggest that (90)Y-Bz-DTPA-AMB8LK is a good candidate for further therapeutic efficacy studies.
胰腺癌的预后非常差,5年生存率低于5%。到目前为止,单独使用外照射放疗或化疗,或两者联合使用,都没有取得令人鼓舞的结果。一种可能的解决方案或许来自靶向治疗的应用,比如放射免疫疗法。我们在此展示了一种新型抗铁蛋白单克隆抗体(Ab)AMB8LK临床前研发所获得的结果。铁蛋白在胰腺癌中过度表达,因此可作为在肿瘤部位递送放射性物质的靶点。AMB8LK抗体与三种螯合剂缀合:2-(4-异硫氰酸苄基)-二亚乙基三胺五乙酸(PSCN-Bz-DTPA)、(R)-2-氨基-3-(4-异硫氰酸苯丙基)-反式-(S,S)-环己烷-1,2-二胺五乙酸(p5CN-Bz-CHX-A"-DTPA)和2-(4-异硫氰酸苄基)-1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸(pSCN-Bz-DOTA)。分析了三种免疫缀合物用铟111和钇90进行放射性标记的情况,以及它们的体外稳定性和对纯铁蛋白及表达铁蛋白的细胞的免疫反应性。在正常小鼠和荷人胰腺腺癌CAPAN-1肿瘤的小鼠身上进行了体内生物分布研究。这些实验证明了这三种化合物具有良好的放射性标记(>95%)、稳定性和免疫反应性。在生物分布研究中,三种免疫缀合物在血液清除率以及在肿瘤、肝脏和骨骼摄取方面存在明显差异。观察到了非常好的胰腺腺癌肿瘤靶向性,尤其是Bz-DTPA-AMB8LK:注射铟标记化合物后3天,为注射剂量的20%;注射钇标记抗体后5天,为注射剂量后的15%。总之,这些动物模型实验结果表明,(90)Y-Bz-DTPA-AMB8LK是进一步进行治疗效果研究的良好候选物。