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Inhibition of tumor growth by plant-derived mAb

机译:植物来源的单克隆抗体抑制肿瘤生长

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摘要

The tumor-associated antigen EpCAM (GA733-2) is a highly expressed target on adenocarcinoma cells, as defined by murine mAb CO17-1A. We recently developed a transgenic plant system for the safe and inexpensive production of large quantities of mAb CO17-1A as a future source of clinical-grade protein. Although the glycosylation pattern of plant-derived mAb (mAb~p) CO17-1A differs considerably from that of the mammalian-derived mAb (mAb~M), we show here that the biological activity of both mAbs is quite similar. mAb~p heavy and light chains assembled to bind the recombinant antigen GA733-2E and specifically bound to human SW948 colorectal carcinoma cells expressing the antigen GA733-2 to the same extent as mAb~M. mAb~p was as effective as mAb~M CO17-1A in inhibiting tumor growth of xenotransplanted SW948 cells in nude mice. These results suggest the promise of transgenic plants as a useful alternative way to produce full-size mAb for cancer immunotherapy.
机译:肿瘤相关抗原EpCAM(GA733-2)是腺癌细胞上高表达的靶标,如鼠mAb CO17-1A所定义。我们最近开发了一种转基因植物系统,可安全,廉价地生产大量mAb CO17-1A,作为未来临床级蛋白质的来源。尽管植物来源的mAb(mAb〜p)CO17-1A的糖基化模式与哺乳动物来源的mAb(mAb〜M)的糖基化模式有显着差异,但我们在此处表明两种mAb的生物学活性非常相似。组装的mAb-p重链和轻链结合重组抗原GA733-2E,并与mAb-M相同程度地特异性结合至表达抗原GA733-2的人SW948大肠癌细胞。 mAb〜p在抑制裸鼠异种移植SW948细胞肿瘤生长方面与mAb〜M CO17-1A一样有效。这些结果表明,转基因植物有望成为生产用于癌症免疫疗法的全尺寸单克隆抗体的有用替代方法。

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