首页> 美国卫生研究院文献>The Journal of Experimental Medicine >A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice
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A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice

机译:重组人白细胞介素1受体拮抗剂可提高小鼠致命内毒素血症后的存活率

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摘要

Interleukin 1 (IL-1) is an endogenously produced cytokine that mediates a variety of physiological effects that may be beneficial or deleterious to the host. C57Bl/6 mice treated intravenously with a recently characterized human recombinant receptor antagonist protein to IL-1 (IL-1ra) had improved survival when treated after a lethal Escherichia coli endotoxin (lipopolysaccharide [LPS]) challenge. IL-1ra was effective when treatment was initiated after LPS, and intravenous administration every 4 h for 24 h was required. Serum levels of tumor necrosis factor (TNF) activity after LPS and in vitro TNF cytotoxicity were not altered by treatment with IL-1ra. These experiments provide direct evidence that the lethal effects of LPS may be mediated through the action of IL-1 and that the IL-1ra can provide a new treatment strategy for disease processes mediated via this cytokine.
机译:白介素1(IL-1)是一种内源性产生的细胞因子,可介导可能对宿主有益或有害的多种生理效应。用致死性大肠杆菌内毒素(脂多糖[LPS])攻击后,用最近表征的针对IL-1的人类重组受体拮抗剂蛋白(IL-1ra)静脉内治疗的C57Bl / 6小鼠具有改善的存活率。在LPS后开始治疗时,IL-1ra是有效的,并且需要每4小时静脉输注24小时。用IL-1ra治疗后,LPS后的血清肿瘤坏死因子(TNF)活性水平和体外TNF细胞毒性没有改变。这些实验提供了直接的证据,表明LPS的致死作用可能是通过IL-1的作用介导的,而IL-1ra可以为通过这种细胞因子介导的疾病过程提供新的治疗策略。

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