Mechanisms and Regulation of the Gene-Expression Response to Sepsis

被引:49
作者
Cornell, Timothy T. [1 ]
Wynn, James [2 ]
Shanley, Thomas P. [1 ]
Wheeler, Derek S. [3 ]
Wong, Hector R. [3 ]
机构
[1] Univ Michigan, CS Mott Childrens Hosp, Div Crit Care Med, Ann Arbor, MI 48109 USA
[2] Duke Univ, Childrens Hosp, Div Neonatol, Durham, NC USA
[3] Cincinnati Childrens Hosp Med Ctr, Div Crit Care Med, Cincinnati, OH USA
基金
美国国家卫生研究院;
关键词
genetics; immunity; sepsis; septic shock; epigenetics; 4G/5G PROMOTER POLYMORPHISM; TOLL-LIKE RECEPTOR-4; FC-GAMMA RECEPTOR; SEPTIC SHOCK SUSCEPTIBILITY; URINARY-TRACT-INFECTION; APOPTOTIC CELL-DEATH; PLASMINOGEN-ACTIVATOR-INHIBITOR-1; GENE; ARG753GLN POLYMORPHISM; MENINGOCOCCAL DISEASE; ZINC HOMEOSTASIS;
D O I
10.1542/peds.2009-3274
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Sepsis is defined as the systemic inflammatory response of the human host that is triggered by an invading pathogen. Despite tremendous advances in both our knowledge of and treatment strategies for this syndrome, sepsis remains among the major causes of morbidity and mortality in children worldwide. Thus, we hypothesize that an improved mechanistic understanding obtained via basic and translational science will continue to identify novel therapeutic targets and approaches. As a result, given the central importance of the alterations in gene expression in regulating the human host's physiologic response to a pathogen, we review the complex factors-genetics, transcriptional expression, and epigenetics-that regulate unique gene-expression patterns in pediatric sepsis and septic shock. We anticipate that emerging data from genetic, genomic, and other translation studies in pediatric sepsis will advance our biological understanding of this response and undoubtedly identify targets for newer therapies. Pediatrics 2010; 125: 1248-1258
引用
收藏
页码:1248 / 1258
页数:11
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