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In vitro antigen-induced antigen-specific antibody production in man. Specific and polyclonal components kinetics and cellular requirements

机译:人体体外抗原诱导的抗原特异性抗体生产。特定和多克隆组件动力学和细胞要求

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摘要

A highly specific and reproducible antigen-induced, antigen-specific culture and assay system for antibody production by human peripheral blood B lymphocytes has been developed. The system is clearly T cell and monocyte dependent and is independent of exogenous mitogens. The major factors in our ability to trigger specific antibody production with antigen alone have been the use of extremely low concentrations of antigen in vitro (doses several orders of magnitude below those inducing a peak blastogenic response), careful attention to in vitro cell density and culture vessel geometry, and appreciation of the kinetics of the circulating antigen-inducible B cell repertoire. A dichotomy and overlap between antigen-induced, antigen-specific and antigen-induced, polyclonal responses was observed in the study of doubly immunized individuals. Whereas antibody responses highly specific for the antigen in culture were observed under one set of culture conditions (flat-bottomed vessels, 1.5 x 10(6) cells), switching to another culture system (round-bottomed vessels, 5 x 10(5) cells) resulted in polyclonal responses to antigen. Despite these culture condition-related differences in the induction of antibody synthesis, the suppression of specific antibody production that occurred at high concentrations of antigen was specific only for the antigen in culture. The capability to easily and reproducibly look at truly antigen-induced, antigen specific antibody production should be a major tool in furthering the understanding of human B cell activation and immunoregulation.
机译:已经开发了用于人外周血B淋巴细胞产生抗体的高度特异性和可再现性的抗原诱导的,抗原特异性的培养和测定系统。该系统显然是T细胞和单核细胞依赖性的,并且独立于外源促细胞分裂剂。影响单独使用抗原触发特异性抗体产生的能力的主要因素是在体外使用极低浓度的抗原(剂量低于诱导峰值成胚反应的剂量几个数量级),对体外细胞密度和培养的注意血管的几何形状,以及对循环抗原可诱导B细胞库的动力学的认识。在双重免疫个体的研究中观察到抗原诱导的,抗原特异性的和抗原诱导的多克隆反应之间的二分法和重叠。在一组培养条件下(平底血管,1.5 x 10(6)个细胞)观察到了对培养中的抗原高度特异性的抗体反应,切换到另一个培养系统(圆底血管,5 x 10(5))细胞)导致对抗原的多克隆反应。尽管在诱导抗体合成方面存在这些与培养条件相关的差异,但在高浓度抗原下抑制特异性抗体产生仅对培养中的抗原具有特异性。轻松而可重复地查看真正的抗原诱导的抗原特异性抗体生产的能力应该是进一步了解人类B细胞激活和免疫调节的主要工具。

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