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当宿主防御出现差错时:脓毒症诱导的免疫抑制建模

When host defense goes awry: Modeling sepsis-induced immunosuppression.

作者信息

Hu Scott B, Zider Alexander, Deng Jane C

机构信息

Division of Pulmonary and Critical Care Medicine, Los Angeles, CA.

出版信息

Drug Discov Today Dis Models. 2012;9(1):e33-e38. doi: 10.1016/j.ddmod.2011.09.001.

DOI:10.1016/j.ddmod.2011.09.001
PMID:24052802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3775367/
Abstract

Sepsis is associated with an initial hyperinflammatory state; however, therapeutic trials targeting the inflammatory response have yielded disappointing results. It is now appreciated that septic patients often undergo a period of relative immunosuppression, rendering them susceptible to secondary infections. Interest in this phenomenon has led to the development of animal models to study the immune dysfunction of sepsis. In this review, we analyze the available models of sepsis-induced immunosuppression.

摘要

脓毒症与初始的高炎症状态相关;然而,针对炎症反应的治疗试验结果令人失望。现在人们认识到,脓毒症患者常经历一段相对免疫抑制期,使他们易患继发性感染。对这一现象的关注促使了用于研究脓毒症免疫功能障碍的动物模型的开发。在本综述中,我们分析了现有的脓毒症诱导免疫抑制模型。

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本文引用的文献

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Deaths: preliminary data for 2009.死亡情况:2009年初步数据。
Natl Vital Stat Rep. 2011 Mar;59(4):1-51.
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Endotoxin tolerance represents a distinctive state of alternative polarization (M2) in human mononuclear cells.内毒素耐受代表了人类单核细胞中一种独特的替代性极化(M2)状态。
J Immunol. 2011 Jun 15;186(12):7243-54. doi: 10.4049/jimmunol.1001952. Epub 2011 May 16.
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Programmed death-1 levels correlate with increased mortality, nosocomial infection and immune dysfunctions in septic shock patients.程序性死亡-1 水平与感染性休克患者的死亡率增加、医院感染和免疫功能障碍相关。
Emodin Ameliorates Intestinal Dysfunction by Maintaining Intestinal Barrier Integrity and Modulating the Microbiota in Septic Mice.
大黄素通过维持肠道屏障完整性和调节脓毒症小鼠的微生物群来改善肠道功能障碍。
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Modulation of the sigma-1 receptor-IRE1 pathway is beneficial in preclinical models of inflammation and sepsis.调节 sigma-1 受体-IRE1 通路对炎症和脓毒症的临床前模型有益。
Sci Transl Med. 2019 Feb 6;11(478). doi: 10.1126/scitranslmed.aau5266.
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Qiang-Xin 1 Formula Prevents Sepsis-Induced Apoptosis in Murine Cardiomyocytes by Suppressing Endoplasmic Reticulum- and Mitochondria-Associated Pathways.强心1号方通过抑制内质网和线粒体相关途径预防脓毒症诱导的小鼠心肌细胞凋亡。
Front Pharmacol. 2018 Jul 30;9:818. doi: 10.3389/fphar.2018.00818. eCollection 2018.
8
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J Vis Exp. 2010 Dec 18(46):2299. doi: 10.3791/2299.
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Am J Respir Crit Care Med. 2011 Apr 1;183(7):932-40. doi: 10.1164/rccm.201006-0934OC. Epub 2010 Oct 19.
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