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Development of humanized rabbit monoclonal antibodies against vascular endothelial growth factor receptor 2 with potential antitumor effects

机译:抗血管内皮生长因子受体2人源化兔单克隆抗体的研制

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摘要

Vascular endothelial growth factor-A (VEGF-A) plays a critical role in physiologic and pathologic angiogenesis through its receptors especially through VEGFR2. The lack of cross-reactivity of monoclonal antibodies with human VEGFR2/mouse Flk-1 is a major obstacle in preclinical developments. In this study, using a unique hybridoma technique, we generated a panel of 30 neutralization anti-VEGFR2 rabbit monoclonal antibodies (RabMAbs) either blocking VEGF/VEGFR2 interaction or inhibiting VEGF-stimulated VEGFR2 tyrosine kinase phosphorylation. Among 18 RabMAbs with human/mouse VEGFR2 cross-reactivity, we humanized one lead candidate RabMAb by Mutational Lineage Guided (MLG) method and further demonstrated its potent inhibition of tumor growth in xenograft mouse model. Our study suggests that RabMAbs are highly relevant for therapeutic applications.
机译:血管内皮生长因子-A(VEGF-A)通过其受体,特别是通过VEGFR2,在生理和病理性血管生成中起关键作用。单克隆抗体与人VEGFR2 /小鼠Flk-1缺乏交叉反应性是临床前发展的主要障碍。在这项研究中,使用独特的杂交瘤技术,我们产生了30种中和性抗VEGFR2兔单克隆抗体(RabMAb),可阻断VEGF / VEGFR2相互作用或抑制VEGF刺激的VEGFR2酪氨酸激酶磷酸化。在具有人/鼠VEGFR2交叉反应性的18种RabMAb中,我们通过突变谱系引导(MLG)方法将一名主要候选RabMAb人源化,并进一步证明了其在异种移植小鼠模型中对肿瘤生长的有效抑制作用。我们的研究表明,RabMAb与治疗应用高度相关。

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