O'Shannessy Daniel J, Smith Michael F, Somers Elizabeth B, Jackson Stephen M, Albone Earl, Tomkowicz Brian, Cheng Xin, Park Young, Fernando Danielle, Milinichik Andrew, Kline Brad, Fulton Regan, Oberoi Pankaj, Nicolaides Nicholas C
Morphotek, Inc., Exton, PA, USA.
PhenoPath, Seattle, WA, USA.
Oncotarget. 2016 Oct 25;7(43):69420-69435. doi: 10.18632/oncotarget.11018.
Endosialin (Tumor Endothelial Marker-1 (TEM-1), CD248) is primarily expressed on pericytes of tumor-associated microvasculature, tumor-associated stromal cells and directly on tumors of mesenchymal origin, including sarcoma and melanoma. While the function of endosialin/TEM-1 is incompletely understood, studies have suggested a role in supporting tumor growth and invasion thus making it an attractive therapeutic target. In an effort to further understand its role in cancer, we previously developed a humanized anti-endosialin/TEM-1 monoclonal antibody (mAb), called ontuxizumab (MORAb-004) for testing in preclinical and clinical studies. We herein report on the generation of an extensive panel of recombinant endosialin/TEM-1 protein extracellular domain (ECD) fragments and novel mAbs against ECD motifs. The domain-specific epitopes were mapped against ECD sub-domains to identify those that can detect distinct structural motifs and can be potentially formatted as probes suitable for diagnostic and functional studies. A number of mAbS were shown to cross-react with the murine and human protein, potentially allowing their use in human animal models and corresponding clinical trials. In addition, pairing of several mAbs supported their use in immunoassays that can detect soluble endosialin/TEM-1 (sEND) in the serum of healthy subjects and cancer patients.
内皮唾液酸蛋白(肿瘤内皮标志物-1(TEM-1),CD248)主要表达于肿瘤相关微血管的周细胞、肿瘤相关基质细胞以及直接表达于间充质来源的肿瘤,包括肉瘤和黑色素瘤。虽然内皮唾液酸蛋白/TEM-1的功能尚未完全明确,但研究表明其在支持肿瘤生长和侵袭方面发挥作用,因此使其成为一个有吸引力的治疗靶点。为了进一步了解其在癌症中的作用,我们之前开发了一种人源化抗内皮唾液酸蛋白/TEM-1单克隆抗体(mAb),称为ontuxizumab(MORAb-004),用于临床前和临床研究测试。我们在此报告了一系列重组内皮唾液酸蛋白/TEM-1蛋白细胞外结构域(ECD)片段的产生以及针对ECD基序的新型单克隆抗体。针对ECD亚结构域绘制了结构域特异性表位,以识别那些能够检测不同结构基序且有可能被构建为适用于诊断和功能研究的探针。许多单克隆抗体被证明可与小鼠和人类蛋白发生交叉反应,这可能使其可用于人类动物模型及相应的临床试验。此外,几种单克隆抗体的配对支持它们用于免疫测定,该免疫测定可检测健康受试者和癌症患者血清中的可溶性内皮唾液酸蛋白/TEM-1(sEND)。