Mechanisms of sepsis-induced organ dysfunction

被引:449
作者
Abraham, Edward
Singer, Mervyn [1 ]
机构
[1] Univ Alabama Birmingham, Sch Med, Dept Med, Birmingham, AL 35200 USA
[2] UCL, Bloomsbury Inst Intens Care Med, Wolfson Inst Biomed Res, London, England
[3] UCL, Dept Med, London, England
基金
英国医学研究理事会;
关键词
sepsis; multiple organ failure; pathogenesis;
D O I
10.1097/01.CCM.0000282072.56245.91
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
Background: The past several years have seen remarkable advances in understanding the basic cellular and physiologic mechanisms underlying organ dysfunction and recovery relating to sepsis. Although several new therapeutic approaches have improved outcome in septic patients, the far-reaching potential of these new insights into sepsis-associated mechanisms is only beginning to be realized. Aim: The Brussels Round Table Conference in 2006 convened >30 experts in the field of inflammation and sepsis to review recent advances involving sepsis and to discuss directions that the field is likely to take in the near future. Findings: Current understanding of the pathophysiology underlying sepsis-induced multiple organ dysfunction highlights the multiple cell populations and cell-signaling pathways involved in this complex condition. There is an increasing appreciation of interactions existing between different cells and organs affected by the septic process. The intricate cross-talk provided by temporal changes in mediators, hormones, metabolites, neural signaling, alterations in oxygen delivery and utilization, and by modifications in cell phenotypes underlines the adaptive and even coordinated processes beyond the dysregulated chaos in which sepsis was once perceived. Many pathologic processes previously considered to be detrimental are now viewed as potentially protective. Applying systems approaches to these complex processes will permit better appreciation of the effectiveness or harm of treatments, both present and future, and also will allow development not only of better directed, but also of more appropriately timed, strategies to improve outcomes from this still highly lethal condition.
引用
收藏
页码:2408 / 2416
页数:9
相关论文
共 108 条
[1]
Alterations in cell signaling in sepsis [J].
Abraham, E .
CLINICAL INFECTIOUS DISEASES, 2005, 41 :S459-S464
[2]
Adib-Conquy M, 2001, J LEUKOCYTE BIOL, V70, P30
[3]
NF-κB expression in mononuclear cells of patients with sepsis resembles that observed in lipopolysaccharide tolerance [J].
Adib-Conquy, M ;
Adrie, C ;
Moine, P ;
Asehnoune, K ;
Fitting, C ;
Pinsky, MR ;
Dhainaut, JF ;
Cavaillon, JM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (05) :1877-1883
[4]
The role of the endothelium in severe sepsis and multiple organ dysfunction syndrome [J].
Aird, WC .
BLOOD, 2003, 101 (10) :3765-3777
[5]
Selenium in Intensive Care (SIC):: Results of a prospective. randomized, placebo-controlled, multiple-center study in patients with severe systemic inflammatory response syndrome, sepsis, and septic shock [J].
Angstwurm, Matthias W. A. ;
Engelmann, Lothar ;
Zimmermann, Thomas ;
Lehmann, Christian ;
Spes, Christoph H. ;
Abel, Peter ;
Strauss, Richard ;
Meier-Hellmann, Andreas ;
Insel, Rudolf ;
Radke, Joachim ;
Schuettler, Juergen ;
Gaertner, Roland .
CRITICAL CARE MEDICINE, 2007, 35 (01) :118-126
[6]
Iron overload upregulates haem oxygenase 1 in the lung more rapidly than in other tissues [J].
Anning, PB ;
Chen, Y ;
Lamb, NJ ;
Mumby, S ;
Quinlan, GJ ;
Evans, TW ;
Gutteridge, JMC .
FEBS LETTERS, 1999, 447 (01) :111-114
[7]
[Anonymous], 2006, LANCET, DOI DOI 10.1016/S0140-6736(06)69005-3
[8]
TLR4 mutations are associated with endotoxin hyporesponsiveness in humans [J].
Arbour, NC ;
Lorenz, E ;
Schutte, BC ;
Zabner, J ;
Kline, JN ;
Jones, M ;
Frees, K ;
Watt, JL ;
Schwartz, DA .
NATURE GENETICS, 2000, 25 (02) :187-+
[9]
Genetic polymorphisms and sepsis [J].
Arcaroli, J ;
Fessler, MB ;
Abraham, E .
SHOCK, 2005, 24 (04) :300-312
[10]
Variant IRAK-1 haplotype is associated with increased nuclear factor-κB activation and worse outcomes in sepsis [J].
Arcaroli, John ;
Silva, Eliezer ;
Maloney, James P. ;
He, Qianbin ;
Svetkauskaite, Daiva ;
Murphy, James R. ;
Abraham, Edward .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 173 (12) :1335-1341