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The preparation of VEGFR1/CD3 bispecific antibody and its specific cytotoxicity against VEGFR1-positive breast cancer cells

机译:VEGFR1 / CD3双特异性抗体的制备及其对VEGFR1阳性乳腺癌细胞的特异性细胞毒性

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Bispecific antibody (BsAb) has been proved to be a very effective antitumor approach because of its distinctive advantages of immune-mediated cytotoxicity. To enhance the ability to recruit and activate T lymphocytes for tumor-specific killing, we constructed and prepared a recombinant human single-chain Fv bispecific antibody (BsAb), named VEGFR1/CD3 BsAb, targeting VEGFR1 and CD3. The VEGFR1/CD3 BsAb was expressed in CHO-K1 cells and purified by Ni-NTA affinity chromatography. The CD3 and VEGFR1-binding activity of VEGFR1/CD3 BsAb was confirmed by flow cytometry. T lymphocyte activation and proliferation induced by VEGFR1/CD3 BsAb were also demonstrated in vitro. Notably, our VEGFR1/CD3 BsAb presented a powerful and specific killing effect against VEGFR1-positive human breast cancer cell MDA-MB-231 and MDA-MB-435 through activating T lymphocyte at very low concentrations, indicating that it will be a valuable antibody drug for treatment of VEGFR1-positive cancers in the future.
机译:双特异性抗体(BsAb)由于其免疫介导的细胞毒性的独特优势,已被证明是一种非常有效的抗肿瘤方法。为了增强募集和激活T淋巴细胞进行肿瘤特异性杀伤的能力,我们构建并制备了靶向VEGFR1和CD3的重组人单链Fv双特异性抗体(BsAb),名为VEGFR1 / CD3 BsAb。 VEGFR1 / CD3 BsAb在CHO-K1细胞中表达,并通过Ni-NTA亲和层析纯化。通过流式细胞术证实了VEGFR1 / CD3 BsAb的CD3和VEGFR1结合活性。还证实了VEGFR1 / CD3 BsAb诱导的T淋巴细胞活化和增殖。值得注意的是,我们的VEGFR1 / CD3 BsAb通过非常低的浓度激活T淋巴细胞对VEGFR1阳性的人乳腺癌细胞MDA-MB-231和MDA-MB-435表现出强大而特异性的杀伤作用,表明它将是有价值的抗体将来可用于治疗VEGFR1阳性癌症的药物。

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