Zhu Z, Rockwell P, Lu D, Kotanides H, Pytowski B, Hicklin D J, Bohlen P, Witte L
Department of Molecular and Cell Biology, ImClone Systems Inc., New York, New York 10014, USA.
Cancer Res. 1998 Aug 1;58(15):3209-14.
A single-chain antibody phage display library was constructed from spleen cells of mice immunized with a soluble form of a human vascular endothelial growth factor (VEGF) receptor, kinase insert domain-containing receptor (KDR). After two rounds of biopanning, >90% of the clones recovered were specifically reactive to KDR. Subsequent selection identified two clones that blocked VEGF binding to KDR. The clones were expressed in Escherichia coli and purified as soluble single-chain Fv (scFv) antibodies. The affinities of the scFv for binding to KDR were determined by BIAcore analysis (2.1 x 10(-9)-5.9 x 10(-9) M). One scFv, p1C11, was shown to inhibit VEGF-induced KDR phosphorylation and VEGF-stimulated DNA synthesis in human umbilical vein endothelial cells. There is much experimental evidence to suggest that the VEGF/KDR/Flk-1 pathway plays an important role in tumor angiogenesis, a process that is essential for tumor growth and metastasis. The antibodies discussed here, which block VEGF binding to KDR, have potential clinical application in the treatment of cancer and other diseases where pathological angiogenesis is involved.
用人血管内皮生长因子(VEGF)受体含激酶插入结构域受体(KDR)的可溶性形式免疫小鼠,从其脾细胞构建了单链抗体噬菌体展示文库。经过两轮生物淘选,回收的克隆中>90%对KDR具有特异性反应性。随后的筛选鉴定出两个能阻断VEGF与KDR结合的克隆。这些克隆在大肠杆菌中表达,并作为可溶性单链Fv(scFv)抗体进行纯化。通过BIAcore分析确定了scFv与KDR结合的亲和力(2.1×10⁻⁹ - 5.9×10⁻⁹ M)。其中一个scFv,p1C11,被证明能抑制人脐静脉内皮细胞中VEGF诱导的KDR磷酸化和VEGF刺激的DNA合成。有许多实验证据表明,VEGF/KDR/Flk-1途径在肿瘤血管生成中起重要作用,而肿瘤血管生成是肿瘤生长和转移所必需的过程。本文讨论的阻断VEGF与KDR结合的抗体在治疗涉及病理性血管生成的癌症和其他疾病方面具有潜在的临床应用价值。