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与白细胞介素-1受体相关激酶-M上调相关的免疫抑制可预测革兰阴性菌败血症(类鼻疽)的死亡率。

Immunosuppression associated with interleukin-1R-associated-kinase-M upregulation predicts mortality in Gram-negative sepsis (melioidosis).

作者信息

Wiersinga Willem Joost, van't Veer Cornelis, van den Pangaart Petra S, Dondorp Arjen M, Day Nicholas P, Peacock Sharon J, van der Poll Tom

机构信息

Center for Infection and Immunity Amsterdam, University of Amsterdam, Amsterdam, the Netherland.

出版信息

Crit Care Med. 2009 Feb;37(2):569-76. doi: 10.1097/CCM.0b013e318194b1bf.

Abstract

OBJECTIVES

Sepsis is associated with immunosuppression (characterized by a reduced capacity of circulating monocytes to release proinflammatory cytokines), which has been implicated in late mortality. Melioidosis, caused by the Gram-negative bacterium Burkholderia pseudomallei, is an important cause of community-acquired sepsis in Southeast Asia with a mortality of up to 40%. Previous in vitro and murine studies have suggested a key role for the so-called negative regulators of the toll-like receptor (TLR) signaling pathway in immunosuppression. In this study, we investigated the expression of these negative TLR regulators in patients with septic melioidosis in association with the responsiveness of peripheral blood leukocytes of these patients to lipopolysaccharide and B. pseudomallei.

DESIGN

Ex vivo study.

SETTING

Academic research laboratory.

PATIENTS

Thirty-two healthy controls and 34 patients with sepsis caused by B. pseudomallei.

INTERVENTIONS

None.

MEASUREMENTS

  1. Plasma cytokine levels; 2) ex vivo cytokine production capacity of whole blood; and 3) purified mononuclear cell-derived messenger RNA (mRNA) levels of key inhibitory molecules of the TLR-signaling cascade were investigated.

MAIN RESULTS

In accordance with an immunosuppressed state, whole blood of patients demonstrated a strongly decreased capacity to release the proinflammatory cytokines tumor necrosis factor-[alpha], interleukin-1[beta], and the chemokine interleukin-8 after ex vivo stimulation with lipopolysaccharide or B. pseudomallei. Analysis of myeloid-differentiation-88-short, interleukin-1R-associated-kinase (IRAK)-M, IRAK-1, suppressor-of-cytokine signaling-3, Src-homology-2-domain-containing inositol-5-phosphatase-1, single-immunoglobulin-interleukin-1R-related-molecule, and A20 mRNA expression in purified mononuclear cells showed decreased IRAK-1 and elevated IRAK-M expression in patients with septic melioidosis. Immunosuppression was correlated with mortality; furthermore, patients who eventually died had higher IRAK-M mRNA levels on admission than the patients who survived.

CONCLUSIONS

Immunosuppression in sepsis caused by B. pseudomallei is associated with an upregulation of IRAK-M and an indicator of poor outcome.

摘要

目的

脓毒症与免疫抑制相关(其特征为循环单核细胞释放促炎细胞因子的能力降低),这与晚期死亡率有关。由革兰氏阴性菌伯克霍尔德菌引起的类鼻疽是东南亚社区获得性脓毒症的重要病因,死亡率高达40%。先前的体外和小鼠研究表明,Toll样受体(TLR)信号通路的所谓负调节因子在免疫抑制中起关键作用。在本研究中,我们调查了脓毒症类鼻疽患者中这些TLR负调节因子的表达,并将这些患者外周血白细胞对脂多糖和伯克霍尔德菌的反应性与之关联起来。

设计

体外研究。

地点

学术研究实验室。

患者

32名健康对照者和34名由伯克霍尔德菌引起脓毒症的患者。

干预措施

无。

测量指标

1)血浆细胞因子水平;2)全血的体外细胞因子产生能力;3)研究TLR信号级联关键抑制分子的纯化单核细胞衍生信使核糖核酸(mRNA)水平。

主要结果

与免疫抑制状态一致,患者的全血在经脂多糖或伯克霍尔德菌体外刺激后,释放促炎细胞因子肿瘤坏死因子-α、白细胞介素-1β和趋化因子白细胞介素-8 的能力显著降低。对纯化单核细胞中髓样分化因子88-短链、白细胞介素-1受体相关激酶(IRAK)-M、IRAK-1、细胞因子信号转导抑制因子-3、含Src同源2结构域的肌醇-5-磷酸酶-1、单免疫球蛋白白细胞介素-1受体相关分子和A20 mRNA表达的分析显示,脓毒症类鼻疽患者的IRAK-1表达降低,IRAK-M表达升高。免疫抑制与死亡率相关;此外,最终死亡的患者入院时的IRAK-M mRNA水平高于存活患者。

结论

伯克霍尔德菌引起的脓毒症中的免疫抑制与IRAK-M的上调相关,是预后不良的一个指标。

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