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首页> 外文期刊>International journal of proteomics >Cladribine and Fludarabine Nucleoside Change the Levels of CD Antigens on B-Lymphoproliferative Disorders
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Cladribine and Fludarabine Nucleoside Change the Levels of CD Antigens on B-Lymphoproliferative Disorders

机译:克拉屈滨和氟达拉滨核苷可改变B淋巴细胞增生性疾病CD抗原的水平

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The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μM, 24 hours), significantly changed the levels of some surface antigens on the human B-cell lines MEC2 and Raji. Changes in the surface proteins were identified using a Cluster of Differentiation (CD) antibody microarray that captures live cells and confirmed by flow cytometry. For Raji cells, CdA up-regulated CD10, CD54, CD80, and CD86, with repression of CD22, while FdA up-regulated CD20, CD54, CD80, CD86 and CD95. For MEC2 cells, CdA up-regulated CD11a, CD20, CD43, CD45, CD52, CD54, CD62L, CD80, CD86, and CD95, but FdA had no effect. Up-regulation of particular CD antigens induced on a B-cell lymphoproliferative disorder by a purine analog could provide targets for therapeutic antibodies with synergistic cell killing.
机译:嘌呤类似物氟达拉滨核苷(FdA)和克拉屈滨(CdA)(1μm,24小时)显着改变了人类B细胞系MEC2和Raji上某些表面抗原的水平。使用捕获活细胞并通过流式细胞仪确认的分化簇(CD)抗体微阵列识别表面蛋白的变化。对于Raji细胞,CdA上调CD10,CD54,CD80和CD86,同时抑制CD22,而FdA上调CD20,CD54,CD80,CD86和CD95。对于MEC2细胞,CdA上调CD11a,CD20,CD43,CD45,CD52,CD54,CD62L,CD80,CD86和CD95,但FdA无效。嘌呤类似物对B细胞淋巴增生性疾病诱导的特定CD抗原的上调可能为具有协同杀伤作用的治疗性抗体提供靶点。

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