首页> 美国卫生研究院文献>Haematologica >The novel CD19-targeting antibody-drug conjugate huB4-DGN462 shows improved anti-tumor activity compared to SAR3419 in CD19-positive lymphoma and leukemia models
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The novel CD19-targeting antibody-drug conjugate huB4-DGN462 shows improved anti-tumor activity compared to SAR3419 in CD19-positive lymphoma and leukemia models

机译:在CD19阳性淋巴瘤和白血病模型中与SAR3419相比靶向CD19的新型抗体-药物偶联物huB4-DGN462显示出改善的抗肿瘤活性

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摘要

Antibody-drug conjugates (ADC) are a novel way to deliver potent cytotoxic compounds to cells expressing a specific antigen. Four ADC targeting CD19, including SAR3419 (coltuximab ravtansine), have entered clinical development. Here, we present huB4-DGN462, a novel ADC based on the SAR3419 anti-CD19 antibody linked via sulfo-SPDB to the potent DNA-alkylating agent DGN462. huB4-DGN462 had improved in vitro anti-proliferative and cytotoxic activity compared to SAR3419 across multiple B-cell lymphoma and human acute lymphoblastic leukemia cell lines. In vivo experiments using lymphoma xenografts models confirmed the in vitro data. The response of B-cell lymphoma lines to huB4-DGN462 was not correlated with CD19 expression, the presence of BCL2 or MYC translocations, TP53 inactivation or lymphoma histology. In conclusion, huB4-DGN462 is an attractive candidate for clinical investigation in patients with B-cell malignancies.
机译:抗体-药物偶联物(ADC)是将有效的细胞毒性化合物传递至表达特定抗原的细胞的新颖方法。包括SAR3419(coltuximab ravtansine)在内的四种靶向CD19的ADC已进入临床开发阶段。在这里,我们介绍了huB4-DGN462,这是一种基于SAR3419抗CD19抗体的新型ADC,该抗体通过磺基SPDB连接至有效的DNA烷基化剂DGN462。与SAR3419相比,在多个B细胞淋巴瘤和人类急性淋巴细胞白血病细胞系中,huB4-DGN462具有改善的体外抗增殖和细胞毒性活性。使用淋巴瘤异种移植物模型的体内实验证实了体外数据。 B细胞淋巴瘤细胞系对huB4-DGN462的反应与CD19表达,BCL2或MYC易位,TP53失活或淋巴瘤组织学无关。总之,huB4-DGN462是B细胞恶性肿瘤患者临床研究的诱人候选人。

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