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Single domain based bispecific antibody Muc1-Bi-1 and its humanized form Muc1-Bi-2 induce potent cancer cell killing in muc1 positive tumor cells

机译:基于单域的双特异性抗体Muc1-Bi-1及其人源化形式Muc1-Bi-2在muc1阳性肿瘤细胞中诱导有效的癌细胞杀伤

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摘要

Muc1 is one of the most studied tumor antigens. However, antibodies or antibody-toxin conjugates against Muc1 have not shown significant efficacy for tumors with Muc1 overexpression. In this study, we employed bispecific antibody approach to target Muc1 positive tumor cells. A novel bispecific antibody, Muc1-Bi-1, was constructed by linking single domain antibodies, anti-Muc1-VHH and anti-CD16-VHH. Muc1-Bi-2, the humanized form of Muc1-Bi-1, was also constructed by grafting. Both Muc1-Bi bispecific antibodies can be efficiently expressed and purified from bacteria. In vitro, the Muc1-Bi bispecific antibodies can recruit Natural Killer (NK) cells to drive potent and specific cell killing of Muc1-overexpressing tumor cells. In xenograft model, the Muc1-Bi bispecific antibodies can suppress tumor growth in the presence of human peripheral blood mononuclear cells (PBMC). These data suggested that the single domain based Muc1-Bi may provide a valid strategy for targeting tumors with Muc1 overexpression.
机译:Muc1是研究最多的肿瘤抗原之一。但是,针对Muc1的抗体或抗体-毒素偶联物对于具有Muc1过表达的肿瘤尚未显示出明显的疗效。在这项研究中,我们采用了双特异性抗体的方法来靶向Muc1阳性肿瘤细胞。通过连接单域抗体,抗Muc1-VHH和抗CD16-VHH,构建了新型双特异性抗体Muc1-Bi-1。 Muc1-Bi-2,Muc1-Bi-1的人源化形式,也通过嫁接构建。 Muc1-Bi双特异性抗体均可有效表达并从细菌中纯化。在体外,Muc1-Bi双特异性抗体可以募集Natural Killer(NK)细胞来驱动对Muc1过表达的肿瘤细胞的有效和特异性杀伤。在异种移植模型中,Muc1-Bi双特异性抗体可以在人外周血单核细胞(PBMC)存在的情况下抑制肿瘤的生长。这些数据表明,基于单结构域的Muc1-Bi可能为靶向具有Muc1过表达的肿瘤提供有效策略。

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