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中毒性休克综合征毒素1作为人肿瘤坏死因子和γ干扰素的诱导剂。

Toxic shock syndrome toxin 1 as an inducer of human tumor necrosis factors and gamma interferon.

作者信息

Jupin C, Anderson S, Damais C, Alouf J E, Parant M

机构信息

Laboratory of Immunopharmacology, Institut Biomédical des Cordeliers, Paris, France.

出版信息

J Exp Med. 1988 Mar 1;167(3):752-61. doi: 10.1084/jem.167.3.752.

Abstract

We present evidence that toxic shock syndrome toxin 1 (TSST-1) induces the production of high levels of TNF by human blood monocytes. Enriched lymphocyte preparations incubated with the staphylococcal toxin produced significant levels of TNF-like activity that is not neutralized by anti-rHuTNF antibodies and is likely to be lymphotoxin (LT or TNF-beta). We demonstrate also that TSST-1 is a potent inducer of IFN-gamma. When lymphocyte preparations were costimulated with PMA, the TSST-1 effect was strongly potentiated and the levels of cytotoxic factors, IFN-gamma, and IL-2 present in supernatant fluids were comparable to those observed after treatment with PMA and PHA. Thus, TSST-1, which is also known as an inducer of IL-1 and IL-2, stimulates the production of endogenous mediators that could play a role in the physiopathological processes of toxic shock syndrome (TSS). The described results suggest that the discrepancies in the clinical features between TSS and endotoxin shock may be related to qualitative differences in cytokine production.

摘要

我们提供的证据表明,中毒性休克综合征毒素1(TSST-1)可诱导人血单核细胞产生高水平的肿瘤坏死因子(TNF)。与葡萄球菌毒素一起孵育的富集淋巴细胞制剂产生了显著水平的TNF样活性,这种活性不能被抗rHuTNF抗体中和,可能是淋巴毒素(LT或TNF-β)。我们还证明TSST-1是γ干扰素(IFN-γ)的有效诱导剂。当淋巴细胞制剂用佛波酯(PMA)进行共刺激时,TSST-1的作用被强烈增强,上清液中存在的细胞毒性因子、IFN-γ和白细胞介素-2(IL-2)的水平与用PMA和植物血凝素(PHA)处理后观察到的水平相当。因此,TSST-1也被认为是白细胞介素-1(IL-1)和IL-2的诱导剂,它能刺激内源性介质的产生,这些介质可能在中毒性休克综合征(TSS)的生理病理过程中发挥作用。所述结果表明,TSS和内毒素休克临床特征的差异可能与细胞因子产生的质的差异有关。

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