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用葡萄球菌超抗原在人B细胞培养物中诱导IgE和IgG1:辅助性T细胞相互作用的作用、对γ干扰素的抗性

Induction of IgE and IgG1 in human B cell cultures with staphylococcal superantigens: role of helper T cell interaction, resistance to interferon-gamma.

作者信息

Armerding D, van Reijsen F C, Hren A, Mudde G C

机构信息

Sandoz Research Institute, Vienna, Austria.

出版信息

Immunobiology. 1993 Jul;188(3):259-73. doi: 10.1016/S0171-2985(11)80234-2.

Abstract

Non-antigen-specific activation of human B lymphocytes for IgE production in vitro requires the presence of interleukin 4 and non-cognate physical interaction with T cells. The latter can be replaced by antibodies directed against the B cells' CD40 structure. Antigen-specific induction of immunoglobulin responses, including IgE, is difficult in human lymphocyte cultures. Thus, we developed a model system which might resemble physiological B lymphocyte stimulation by antigen. Co-cultures of purified tonsillar B cells from normal donors with non-HLA matched T helper clones obtained from the skin of atopic dermatitis patients produced significant levels of IgE and IgG1 after stimulation with appropriate types of staphylococcal exotoxins, provided that IL-4 was also induced in the T cells. Such responses were further enhanced by addition of low doses of anti-CD40 antibodies. Concentrations of anti-CD40, optimal for stimulation of B cells in the absence of T helper lymphocytes, were less effective in this regard and even inhibitory in some experiments. Most powerful immunoglobulin induction was observed when the cultures were spiked with low amounts of IL-4 and anti-CD40 which did not elicit substantial immunoglobulin production in the absence of the staphylococcal exotoxins. Induction of IL-2 in T/B cell cultures by superantigens without production of appreciable quantities of IL-4 provoked considerable IgG1 titer but no IgE. High amounts of interferon-gamma generated by the T cells in vitro in the presence of superantigens did not appear to interfere with immunoglobulin induction. Addition of recombinant interferon at the beginning of the culture period at doses which effectively suppressed IL-4 plus anti-CD40 induced immunoglobulin responses did not inhibit T helper and superantigen dependent B cell activation. Superantigen mediated B cell stimulation for immunoglobulin production was dependent on cell-cell contact. The experimental results presented suggest that this cellular interaction did not necessarily involve T-B cell bridging by superantigens.

摘要

人B淋巴细胞在体外产生IgE的非抗原特异性激活需要白细胞介素4的存在以及与T细胞的非同源物理相互作用。后者可以被针对B细胞CD40结构的抗体所取代。在人淋巴细胞培养物中,包括IgE在内的免疫球蛋白反应的抗原特异性诱导很困难。因此,我们开发了一个可能类似于抗原对生理性B淋巴细胞刺激的模型系统。来自正常供体的纯化扁桃体B细胞与从特应性皮炎患者皮肤获得的非HLA匹配的T辅助克隆共培养,在用适当类型的葡萄球菌外毒素刺激后,产生了显著水平的IgE和IgG1,前提是T细胞中也诱导了IL-4。通过添加低剂量的抗CD40抗体,这种反应进一步增强。在没有T辅助淋巴细胞的情况下,对B细胞刺激最有效的抗CD40浓度在这方面效果较差,甚至在某些实验中具有抑制作用。当培养物中加入少量IL-4和抗CD40时,观察到最强的免疫球蛋白诱导,而在没有葡萄球菌外毒素的情况下,它们不会引发大量免疫球蛋白产生。超抗原在T/B细胞培养物中诱导IL-2但不产生大量IL-4,引发了相当高的IgG1滴度,但没有IgE。在超抗原存在下,T细胞在体外产生的大量干扰素-γ似乎不会干扰免疫球蛋白诱导。在培养期开始时添加重组干扰素,其剂量能有效抑制IL-4加抗CD40诱导的免疫球蛋白反应,但不会抑制T辅助细胞和超抗原依赖的B细胞激活。超抗原介导的B细胞刺激产生免疫球蛋白依赖于细胞间接触。所呈现的实验结果表明,这种细胞间相互作用不一定涉及超抗原介导的T-B细胞桥接。

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