Division of Critical Care Medicine, C.S. Mott Children's Hospital, University of Michigan, Ann Arbor, MI, USA.
Pediatrics. 2010 Jun;125(6):1248-58. doi: 10.1542/peds.2009-3274. Epub 2010 May 17.
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.
败血症被定义为人体宿主对入侵病原体的全身性炎症反应。尽管我们在该综合征的认识和治疗策略方面取得了巨大进展,但败血症仍然是全球儿童发病率和死亡率的主要原因之一。因此,我们假设通过基础和转化科学获得的更深入的机制理解将继续确定新的治疗靶点和方法。因此,鉴于基因表达的改变在调节人体宿主对病原体的生理反应方面的重要性,我们回顾了调节儿科败血症和感染性休克中独特基因表达模式的复杂因素——遗传学、转录表达和表观遗传学。我们预计,儿科败血症中遗传、基因组和其他转化研究的新数据将增进我们对这种反应的生物学理解,并无疑确定新疗法的靶点。