抗原诱导辅助因子体外合成抗体的特异性及其与淋巴细胞相互作用的关系。

N Khansari, H H Fudenberg
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引用次数: 2

摘要

体外实验表明,PWM和抗原可刺激人外周血b细胞产生特异性抗体。这种刺激依赖于t细胞和抗原的存在。然而,T细胞可以被一种可溶性因子取代,这种可溶性因子来源于用PWM和/或抗原培养48小时的T细胞。在没有抗原的情况下,辅助因子作为一种多克隆激活剂,引起b细胞的最小增殖。当抗原存在时,特异性抗体的产生不依赖于辅助因子的来源。尽管存在抗原和/或辅助因子,但去除单核细胞会破坏Ig和特异性抗体的合成。虽然总IgG的产生需要自体单核细胞,但辅助因子的来源并不重要。产生特异性抗体需要单核细胞和辅助因子来自同一供体;因此,B细胞、t细胞和单核细胞的合作产生特异性抗体可能受到限制。相反,对于多克隆Ig的生产(在没有抗原的情况下),b细胞和单核细胞与t细胞的合作不是。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Specificity of antigen induced helper factor for antibody synthesis in vitro and its relation to lymphocytes interaction.

Human peripheral blood B-cells can be stimulated with PWM and antigen to produce specific antibody in vitro. This stimulation depends on the presence of T-cells and antigen. T cells, however, can be replaced by a soluble factor derived from a 48-hr culture of T-cells with either PWM and/or antigen. The helper factor, in the absence of antigen, acts as a polyclonal activator causing minimal proliferation of B-cells. When antigen is present, production of specific antibody is not dependent on the source of helper factor. Removal of monocytes abolished synthesis of both Ig and specific antibody although antigen and/or helper factor were present. While production of total IgG required autologous monocytes, the origin of the helper factor was not crucial. Production of specific antibody required that both monocytes and helper factor be derived from the same donor; therefore it seems that cooperation of B-, T-cells and monocytes for production of specific antibody is probably Ia restricted. In contrast, for production of polyclonal Ig (in the absence of antigen), cooperation of B-cells and monocytes with T-cells is not.

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