Ackerman Margaret E, Chalouni Cecile, Schmidt Michael M, Raman Vivek V, Ritter Gerd, Old Lloyd J, Mellman Ira, Wittrup K Dane
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Cancer Immunol Immunother. 2008 Jul;57(7):1017-27. doi: 10.1007/s00262-007-0433-x.
The A33 antigen is a cell surface glycoprotein of the small intestine and colonic epithelium with homology to tight junction-associated proteins of the immunoglobulin superfamily, including CAR and JAM. Its restricted tissue localization and high level of expression have led to its use as a target in colon cancer immunotherapy. Although the antigen is also present in normal intestine, radiolabeled antibodies against A33 are selectively retained by tumors in the gut as well as in metastatic lesions for as long as 6 weeks. Accordingly, we have studied the trafficking and kinetic properties of the antigen to determine its promise in two-step, pretargeted therapies. The localization, mobility, and persistence of the antigen were investigated, and this work has demonstrated that the antigen is both highly immobile and extremely persistent-retaining its surface localization for a turnover halflife of greater than 2 days. In order to explain these unusual properties, we explored the possibility that A33 is a component of the tight junction. The simple property of surface persistence, described here, may contribute to the prolonged retention of the clinically administered antibodies, and their uncommon ability to penetrate solid tumors.
A33抗原是一种小肠和结肠上皮细胞表面糖蛋白,与免疫球蛋白超家族中紧密连接相关蛋白(包括CAR和JAM)具有同源性。其有限的组织定位和高水平表达使其成为结肠癌免疫治疗的靶点。尽管该抗原也存在于正常肠道中,但针对A33的放射性标记抗体在肠道肿瘤以及转移病灶中可选择性保留长达6周。因此,我们研究了该抗原的运输和动力学特性,以确定其在两步预靶向治疗中的前景。对该抗原的定位、流动性和持久性进行了研究,这项工作表明该抗原高度不移动且极其持久——其表面定位的周转半衰期大于2天。为了解释这些不寻常的特性,我们探讨了A33是紧密连接成分的可能性。这里描述的表面持久性这一简单特性,可能有助于临床应用抗体的延长保留及其穿透实体瘤的非凡能力。