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Heterodimeric bispecific single-chain variable-fragment antibodies against EpCAM and CD16 induce effective antibody-dependent cellular cytotoxicity against human carcinoma cells

机译:针对EpCAM和CD16的异二聚体双特异性单链可变片段抗体诱导针对人癌细胞的有效抗体依赖性细胞毒性

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摘要

A heterodimeric bispecific biological recombinant drug was synthesized by splicing DNA fragments from two fully humanized single-chain variable-fragment (scFV) antibody fragments forming a novel drug simultaneously recognizing the CD16 natural killer (NK) cell marker and the cancer marker epithelial cell adhesion molecule (EpCAM). The drug precipitously enhanced the killing of human carcinomas of the prostate, breast, colon, head, and neck even at very low effector:target ratios. The drug EpCAM16 rendered even nonactivated NK cell-proficient killers and activated them to kill via degranulation and cytokine production. Studies show that bispecific antibodies can be used to induce proficient killing of the carcinoma targets that ordinarily are resistant to NK-mediated killing. Apparently, the innate immune system can be effectively recruited to kill cancer cells using the bispecific antibody platform and EpCAM targeting.
机译:通过剪接两个完全人源化的单链可变片段(scFV)抗体片段的DNA片段,从而形成一种同时识别CD16自然杀伤(NK)细胞标志物和癌症标志物上皮细胞粘附分子的新型药物,来合成异二聚体双特异性生物重组药物(EpCAM)。即使在极低的效应子/靶标比率下,该药物也可显着增强对前列腺癌,乳腺癌,结肠癌,头颈癌的杀灭作用。药物EpCAM16甚至提供了非活化的NK细胞杀伤剂,并通过脱颗粒和细胞因子产生将其活化而杀死。研究表明,双特异性抗体可用于诱导杀死通常对NK介导的杀伤具有抗性的癌靶标。显然,可以使用双特异性抗体平台和EpCAM靶向有效招募先天免疫系统以杀死癌细胞。

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