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严重类鼻疽中血浆干扰素(IFN)-γ以及诱导IFN-γ的细胞因子白细胞介素(IL)-18、IL-12和IL-15浓度升高。

Elevated plasma concentrations of interferon (IFN)-gamma and the IFN-gamma-inducing cytokines interleukin (IL)-18, IL-12, and IL-15 in severe melioidosis.

作者信息

Lauw F N, Simpson A J, Prins J M, Smith M D, Kurimoto M, van Deventer S J, Speelman P, Chaowagul W, White N J, van der Poll T

机构信息

Laboratory of Experimental Internal Medicine, Department of Infectious Diseases, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

J Infect Dis. 1999 Dec;180(6):1878-85. doi: 10.1086/315155.

Abstract

Interferon (IFN)-gamma plays an important role in the pathogenesis of sepsis. Production of IFN-gamma is stimulated by synergistic effects of interleukin (IL)-18, IL-12, and IL-15. To investigate the regulation of IFN-gamma production during severe gram-negative infection, the plasma concentrations of IFN-gamma, IL-18, IL-12, and IL-15 were measured in 83 patients with suspected melioidosis. The diagnosis was confirmed in 62 patients, 31 of whom had blood cultures positive for Burkholderia pseudomallei, of whom 12 died. Compared with healthy controls, patients had elevated levels of IFN-gamma, IL-18, IL-12p40, and IL-15 on admission, with significantly higher levels in blood culture-positive patients, and these levels remained elevated during the 72-h study period. In whole blood stimulated with heat-killed B. pseudomallei, anti-IL-12 had a stronger inhibitory effect than anti-IL-18 and anti-IL-15 on IFN-gamma production. This effect of anti-IL-12 was further enhanced by anti-IL-18. These data suggest that during gram-negative sepsis, IFN-gamma production is controlled at least in part by endogenous IL-18, IL-12, and IL-15.

摘要

干扰素(IFN)-γ在脓毒症发病机制中起重要作用。白细胞介素(IL)-18、IL-12和IL-15的协同作用可刺激IFN-γ的产生。为研究严重革兰氏阴性菌感染期间IFN-γ产生的调控机制,我们检测了83例疑似类鼻疽患者血浆中IFN-γ、IL-18、IL-12和IL-15的浓度。62例患者确诊,其中31例血培养伯克霍尔德菌假鼻疽阳性,12例死亡。与健康对照组相比,患者入院时IFN-γ、IL-18、IL-12p40和IL-15水平升高,血培养阳性患者水平显著更高,且在72小时研究期间这些水平持续升高。在用热灭活的伯克霍尔德菌假鼻疽刺激的全血中,抗IL-12对IFN-γ产生的抑制作用比抗IL-18和抗IL-15更强。抗IL-18进一步增强了抗IL-12的这种作用。这些数据表明,在革兰氏阴性菌脓毒症期间,IFN-γ的产生至少部分受内源性IL-18、IL-12和IL-15的控制。

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