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Antigen-specific electrophoretic cell separation (ASECS): isolation by human T and B lymphocyte subpopulations by free-flow electrophoresis after reaction with antibodies

机译:抗原特异性电泳细胞分离(ASECS):与抗体反应后通过自由流动电泳通过人T和B淋巴细胞亚群分离

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摘要

The electrophoretic mobility of human lymphocytes can be reduced by incubation with surface antigen specific antibodies under non-capping conditions. This renders subpopulations of human peripheral blood lymphocytes accessible to separation by free-flow electrophoresis. After reaction of lymphocyte preparations with anti-IgM antibody and a fluorescent second antibody, B lymphocytes showed a considerable shift in position in preparative cell electrophoresis and could be separated with high yield, purity and vitality. Similarly, a T cell subpopulation reactive with the monoclonal antibody T811 could be isolated, even though only small amounts of this antibody were bound, by using a double-sandwich method. Non-specific antibody uptake via Fc-receptors did not contribute to the observed shift of antibody-labelled cells to lower electrophoretic mobility. Flow cytometric analysis showed that cells were separated according to their antigen density. Thus cell electrophoresis can be used to separate antibody-labelled cells. With a flow rate of 100,000 cells/sec this method has a much higher separation capacity than fluorescence-activated cell sorting. The described method should be applicable to the separation of a wide range of cell populations for which specific antibodies are available.
机译:通过在非封闭条件下与表面抗原特异性抗体一起孵育,可以降低人淋巴细胞的电泳迁移率。这使得人外周血淋巴细胞的亚群易于通过自由流动电泳分离。淋巴细胞制品与抗IgM抗体和荧光二抗反应后,B淋巴细胞在制备细胞电泳中显示出明显的位置偏移,并且可以高产率,纯度和活力进行分离。类似地,通过使用双夹心法,即使仅结合少量的该抗体,也可以分离与单克隆抗体T811具有反应性的T细胞亚群。经由Fc受体的非特异性抗体摄取无助于观察到的抗体标记细胞向较低电泳迁移率的转变。流式细胞仪分析表明,根据抗原密度将细胞分离。因此,细胞电泳可用于分离抗体标记的细胞。流速为100,000个细胞/秒,此方法比荧光激活细胞分选具有更高的分离能力。所描述的方法应该适用于分离广泛的具有特定抗体的细胞群。

著录项

  • 作者

    Hansen Ernil; Hannig Kurt;

  • 作者单位
  • 年度 1982
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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