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可溶性微生物抗原应答过程中免疫干扰素产生的调控

Regulation of immune interferon production during the response to soluble microbial antigens.

作者信息

Piccolella E, Dolei A, Lombardi G, Vismara D, Pizzoli P, Colizzi V, Dianzani F

出版信息

Clin Exp Immunol. 1986 Jul;65(1):190-7.

Abstract

Human peripheral blood mononuclear cells (PBMC) stimulated in vitro with purified protein derivative (PPD) or with a Candida albicans polysaccharide extract (MPPS) released immune interferon (IFN) and interleukin 2 (IL-2). Kinetic studies showed a biphasic production of IFN with maximum levels at days 3-4 and days 5-6 of culture. In contrast, the IL-2 production is only observed at days 2-3 of culture. The relationship between IFN and IL-2, analysed both in responder and nonresponder PBMC cultures, showed that the early peak of IFN production appears to be IL-2 independent whereas the second peak seems strictly related to the presence of IL-2 culture. Furthermore, monoclonal antibodies against class I and class II products of the major histocompatibility complex (MHC) inhibited IFN production when added at the beginning of culture, whereas only anti-class I antibodies interfered with the release of IFN when added to antigen-primed lymphocytes.

摘要

用纯化蛋白衍生物(PPD)或白色念珠菌多糖提取物(MPPS)在体外刺激人外周血单核细胞(PBMC),可释放免疫干扰素(IFN)和白细胞介素2(IL-2)。动力学研究显示,IFN呈双相产生,在培养的第3 - 4天和第5 - 6天达到最高水平。相比之下,IL-2仅在培养的第2 - 3天被观察到。在反应者和无反应者PBMC培养物中分析IFN与IL-2之间的关系表明,IFN产生的早期峰值似乎不依赖于IL-2,而第二个峰值似乎与IL-2培养物的存在密切相关。此外,针对主要组织相容性复合体(MHC)I类和II类产物的单克隆抗体在培养开始时添加会抑制IFN的产生,而仅抗I类抗体添加到抗原致敏淋巴细胞中时会干扰IFN的释放。

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