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S3Ab, a novel antibody targeting B lymphocytes, is a potential therapeutic agent for B-lineage malignancies

机译:S3ab是一种靶向B淋巴细胞的新型抗体,是B族分裂恶性肿瘤的潜在治疗剂

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摘要

CD79 alpha protein together with the related CD79 beta protein forms the B-cell antigen receptor (BCR). It remains present when B cells transform into active plasma cells, and is also present in virtually all B cell neoplasms. Monoclonal antibody (mAb) S3 (S3Ab) is a novel anti-CD79 alpha antibody generated by using Raji cells as an immunogen. Herein, we conducted a study on S3Ab using various cellular and immunocytological techniques. The results showed that S3Ab could recognise CD79 alpha in living cells. The molecular weights of the heavy and the light chains of S3Ab were 55 and 26 kDa, respectively. S3 antigen is only expressed on more mature B cells and negative on blast B cells. It could partially block the binding of anti-CD79 alpha (Hm47, recognising the cytoplasmic domain of CD79 alpha) to target cells. Immunoprecipitation experiment showed that S3 antigen is about 33 kDa and S3 can specifically bind to the recombinant extracellular segment of CD79 alpha. The internalisation rate of S3Ab to the target cells was as high as 74.0% after incubation at for 3 h. In conclusion, S3Ab is probably a new target molecule for B cells and can be an excellent antibody in targeting treatment of haematopoietic malignancies, warranting further development of this agent.
机译:CD79α蛋白与相关的CD79β蛋白一起形成B细胞抗原受体(BCR)。当B细胞转化为活性血浆细胞时,它仍然存在,并且在几乎所有B细胞肿瘤中也存在。单克隆抗体(MAB)S3(S3AB)是通过使用Raji细胞作为免疫原产生的新型抗CD79α抗体。在此,我们使用各种细胞和免疫细胞学技术对S3ab进行了研究。结果表明,S3AB可以识别活细胞中的CD79α。 S3ab的重链和轻链的分子量分别为55和26kDa。 S3抗原仅在更成熟的B细胞上表达并在Blast B细胞上表达阴性。它可以部分阻断抗CD79α(HM47,识别CD79α的细胞质结构域)对靶细胞的结合。免疫沉淀实验表明,S3抗原是约33kDa,S3可以特异性结合CD79α的重组细胞外部。在孵育3小时后,S3ab与靶细胞的内化速率高达74.0%。总之,S3AB可能是B细胞的新靶分子,并且可以是靶向血臭恶性肿瘤治疗的优异抗体,需要进一步发展该试剂。

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