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感染性休克患儿入院时血管生成素水平。

Admission angiopoietin levels in children with septic shock.

作者信息

Giuliano John S, Lahni Patrick M, Harmon Kelli, Wong Hector R, Doughty Lesley A, Carcillo Joseph A, Zingarelli Basilia, Sukhatme Vikas P, Parikh Samir M, Wheeler Derek S

机构信息

Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

Shock. 2007 Dec;28(6):650-654.

Abstract

Angiopoietin (angpt) 1 and angpt-2 are circulating proteins first ascribed opposing roles in embryonic angiogenesis. Both bind the tyrosine kinase with immunoglobulin-like loop and epidermal growth factor homology domains (Tie) 2 receptor on endothelial cells, but angpt-1 is a Tie-2 agonist, whereas angpt-2 antagonizes Tie-2 signaling. In the developed vasculature, angpt-1 protects against vascular leak, whereas angpt-2 promotes increased vascular permeability. Because alterations in vascular permeability are common in septic shock, we obtained plasma from critically ill children within 24 h of diagnosis of the systemic inflammatory response syndrome (SIRS, n = 20), sepsis (n = 20), or septic shock (n = 61), as well as 15 healthy controls. Plasma levels of angpt-1 and angpt-2 were measured via a commercially available enzyme-linked immunosorbent assay. Plasma angpt-2 levels were significantly elevated in children with septic shock when compared with healthy children, as well as critically ill children with either SIRS or sepsis, and circulating angpt-2 levels seemed to correlate with disease severity and outcome. In addition, plasma angpt-1 levels were significantly decreased in critically ill children with septic shock compared with critically ill children with either SIRS or sepsis. Given the contrasting effects of angpt-2 and angpt-1 on the vascular endothelium, these two factors may play an important role in the pathophysiology of septic shock in children, and further studies are warranted.

摘要

血管生成素(angpt)1和angpt-2是循环蛋白,最初被认为在胚胎血管生成中发挥相反作用。二者均与内皮细胞上具有免疫球蛋白样环和表皮生长因子同源结构域的酪氨酸激酶(Tie)2受体结合,但angpt-1是Tie-2激动剂,而angpt-2拮抗Tie-2信号传导。在已发育的脉管系统中,angpt-1可防止血管渗漏,而angpt-2则促进血管通透性增加。由于血管通透性改变在感染性休克中很常见,我们在诊断为全身炎症反应综合征(SIRS,n = 20)、脓毒症(n = 20)或感染性休克(n = 61)的危重症儿童发病24小时内采集血浆,同时采集了15名健康对照者的血浆。通过市售的酶联免疫吸附测定法检测血浆中angpt-1和angpt-2的水平。与健康儿童以及患有SIRS或脓毒症的危重症儿童相比,感染性休克儿童的血浆angpt-2水平显著升高,且循环angpt-2水平似乎与疾病严重程度和预后相关。此外,与患有SIRS或脓毒症的危重症儿童相比,感染性休克危重症儿童的血浆angpt-1水平显著降低。鉴于angpt-2和angpt-1对血管内皮的作用相反,这两种因子可能在儿童感染性休克的病理生理学中起重要作用,有必要进一步研究。

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