Scheuer Werner, Thomas Markus, Hanke Petra, Sam Johannes, Osl Franz, Weininger Diana, Baehner Monika, Seeber Stefan, Kettenberger Hubert, Schanzer Jürgen, Brinkmann Ulrich, Weidner K Michael, Regula Jörg, Klein Christian
a Roche Innovation Center Penzberg, Roche Pharma Research and Early Development , Nonnenwald 2, Penzberg , Germany.
b Roche Innovation Center Zurich, Roche Pharma Research and Early Development , Wagistrasse 18, Schlieren , Switzerland.
MAbs. 2016;8(3):562-73. doi: 10.1080/19420862.2016.1147640.
Vascular endothelial growth factor (VEGF)-A blockade has been validated clinically as a treatment for human cancers. Angiopoietin-2 (Ang-2) is a key regulator of blood vessel remodeling and maturation. In tumors, Ang-2 is up-regulated and an unfavorable prognostic factor. Recent data demonstrated that Ang-2 inhibition mediates anti-tumoral effects. We generated a tetravalent bispecific antibody (Ang-2-VEGF-TAvi6) targeting VEGF-A with 2 arms based on bevacizumab (Avastin®), and targeting Ang-2 with 2 arms based on a novel anti-Ang-2 antibody (LC06). The two Ang-2-targeting single-chain variable fragments are disulfide-stabilized and fused to the C-terminus of the heavy chain of bevacizumab. Treatment with Ang-2-VEGF-A-TAvi6 led to a complete abrogation of angiogenesis in the cornea micropocket assay. Metastatic spread and tumor growth of subcutaneous, orthotopic and anti-VEGF-A resistant tumors were also efficiently inhibited. These data further establish Ang-2-VEGF bispecific antibodies as a promising anti-angiogenic, anti-metastatic and anti-tumor agent for the treatment of cancer.
血管内皮生长因子(VEGF)-A阻断疗法已在临床上被验证可用于治疗人类癌症。血管生成素-2(Ang-2)是血管重塑和成熟的关键调节因子。在肿瘤中,Ang-2上调且是一个不良预后因素。最近的数据表明,抑制Ang-2可介导抗肿瘤作用。我们基于贝伐单抗(阿瓦斯汀®)构建了一种双价双特异性抗体(Ang-2-VEGF-TAvi6),其两条臂靶向VEGF-A,另外两条臂基于一种新型抗Ang-2抗体(LC06)靶向Ang-2。两个靶向Ang-2的单链可变片段通过二硫键稳定,并与贝伐单抗重链的C末端融合。在角膜微袋试验中,用Ang-2-VEGF-A-TAvi6治疗可完全消除血管生成。皮下、原位和抗VEGF-A耐药肿瘤的转移扩散和肿瘤生长也得到有效抑制。这些数据进一步证实,Ang-2-VEGF双特异性抗体是一种有前景的抗血管生成、抗转移和抗肿瘤药物,可用于癌症治疗。