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前沿:白细胞介素-15在体内共刺激全身性施瓦茨曼反应和先天性免疫干扰素-γ的产生。

Cutting edge: IL-15 costimulates the generalized Shwartzman reaction and innate immune IFN-gamma production in vivo.

作者信息

Fehniger T A, Yu H, Cooper M A, Suzuki K, Shah M H, Caligiuri M A

机构信息

Department of Internal Medicine, Division of Hematology/Oncology, Comprehensive Cancer Center, Ohio State University, Columbus, USA.

出版信息

J Immunol. 2000 Feb 15;164(4):1643-7. doi: 10.4049/jimmunol.164.4.1643.

Abstract

Sequential administration of LPS to SCID mice results in the generalized Shwartzman reaction, manifesting as rapid mortality via cytokine-induced shock. Here we demonstrate that in vivo neutralization of IL-15 before LPS priming significantly reduced lethality in this reaction (p = 0.0172). We hypothesize that LPS priming induces IL-12 and IL-15 that costimulate NK cell-derived IFN-gamma. Such IFN-gamma may then in turn sensitize macrophages to elicit the Shwartzman reaction following a subsequent LPS challenge. Supporting this, IL-12 and IL-15 synergized to induce murine NK cell IFN-gamma production in vitro. LPS stimulation of SCID mouse splenocytes resulted in measurable IFN-gamma production, which was reduced when IL-15 was neutralized or IL-2/15Rbeta was blocked. Pretreatment with either anti-IL-2/15Rbeta or anti-IL-15 Abs reduced serum IFN-gamma protein following LPS administration to SCID mice. Collectively, these data provide the first in vivo evidence that IL-15 participates in LPS-induced innate immune IFN-gamma production and significantly contributes to the lethal Shwartzman reaction.

摘要

对重症联合免疫缺陷(SCID)小鼠连续给予脂多糖(LPS)会引发全身性施瓦茨曼反应,表现为细胞因子诱导的休克导致快速死亡。在此我们证明,在LPS激发前对白细胞介素-15(IL-15)进行体内中和可显著降低该反应中的致死率(p = 0.0172)。我们推测,LPS激发会诱导IL-12和IL-15,它们共同刺激自然杀伤(NK)细胞衍生的γ干扰素(IFN-γ)。随后,这种IFN-γ可能反过来使巨噬细胞敏感化,从而在后续LPS攻击后引发施瓦茨曼反应。支持这一观点的是,IL-12和IL-15在体外协同诱导小鼠NK细胞产生IFN-γ。LPS刺激SCID小鼠脾细胞会导致可测量的IFN-γ产生,当IL-15被中和或IL-2/15Rβ被阻断时,该产生量会减少。用抗IL-2/15Rβ或抗IL-15抗体进行预处理可降低向SCID小鼠给予LPS后血清中IFN-γ蛋白的水平。总体而言,这些数据提供了首个体内证据,表明IL-15参与LPS诱导的先天性免疫IFN-γ产生,并对致死性施瓦茨曼反应有显著贡献。

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