Ikejima T, Okusawa S, van der Meer J W, Dinarello C A
Department of Medicine, New England Medical Center Hospitals, Boston, Massachusetts 02111.
J Infect Dis. 1988 Nov;158(5):1017-25. doi: 10.1093/infdis/158.5.1017.
A shock-like syndrome was induced in rabbits by administering toxic-shock-syndrome toxin-1 (TSST-1); tumor necrosis factor (TNF)-like activity was detected in sera of rabbits 3.5 h after injection, as measured by cytotoxic effects on the tumorigenic L929 murine fibroblast cell line. Appearance of this activity in sera coincided with onset of significant shock-related hemodynamic changes. TSST-1 stimulated release of TNF-like material from rabbit mononuclear cells in culture. Human mononuclear cells also secreted a cytotoxic substance shown to be TNF by radioimmunoassay. Maximal TNF secretion was higher in human mononuclear cells stimulated with TSST-1 than in those stimulated with bacterial lipopolysaccharide. Lipopolysaccharide, however, was a more potent inducer of interleukin-1 alpha and interleukin-1 beta from the same cells than was TSST-1. Because TNF and interleukin-1 act synergistically during induction of a shock-like state, these results suggest that part of the TSST-1-induced shock is due to production of interleukin-1 and TNF.
通过给予中毒性休克综合征毒素-1(TSST-1)在兔中诱导出一种类似休克的综合征;注射后3.5小时,通过对致瘤性L929小鼠成纤维细胞系的细胞毒性作用检测到兔血清中存在肿瘤坏死因子(TNF)样活性。血清中这种活性的出现与显著的休克相关血流动力学变化的开始相一致。TSST-1刺激培养的兔单核细胞释放TNF样物质。人单核细胞也分泌一种经放射免疫测定显示为TNF的细胞毒性物质。用TSST-1刺激的人单核细胞中TNF的最大分泌量高于用细菌脂多糖刺激的人单核细胞。然而,脂多糖比TSST-1更能诱导同一细胞产生白细胞介素-1α和白细胞介素-1β。由于TNF和白细胞介素-1在诱导类似休克状态时起协同作用,这些结果表明TSST-1诱导的休克部分是由于白细胞介素-1和TNF的产生。