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程序性细胞死亡 1 表达作为危重症手术患者免疫和生理功能障碍的标志物。

Programmed death 1 expression as a marker for immune and physiological dysfunction in the critically ill surgical patient.

机构信息

Department of Surgery, Alpert School of Medicine at Brown, University and Rhode Island Hospital, Providence, Rhode Island, USA.

出版信息

Shock. 2012 Aug;38(2):117-22. doi: 10.1097/SHK.0b013e31825de6a3.

Abstract

Programmed death 1 (PD-1) is an inhibitor protein receptor for the immune system and has been shown to be upregulated in animal models of critical illness as well as after trauma and in burn victims in humans. It is believed that PD-1 may play a role in the immune dysfunction seen in surgical critical illness. However, although prior studies have associated changes in PD-1 expression with altered immune cell function, it is not known if a correlation with clinical status exists. We therefore aimed to describe a potential role for PD-1 in the immune dysfunction seen in critically ill trauma and surgical patients. This is an observational cohort study. Acute Physiology and Chronic Health Evaluation II (APACHE II) scores were calculated on critically ill and injured trauma and surgical intensive care unit patients from a tertiary care/level I trauma center. Blood was drawn within 24 h of establishment of diagnosis and admission to the intensive care unit to measure circulating cytokine levels, as well as PD-1 expression on circulating cells. Main outcome measures included PD-1 expression on leukocytes and the relationship to physiological dysfunction (APACHE II) as well as the correlation of PD-1 expression and interleukin 10 levels among patients with severe physiological dysfunction. Samples were collected from 90 critically ill surgical patients. Among patients with severe physiological dysfunction (APACHE II >20), there were increased numbers of granulocytes (median, 144 vs. 90 cells/μL; P = 0.037) and monocytes (median, 12 vs. 6 cells/μL; P = 0.022) with PD-1 expression. In addition, among patients with an APACHE II score of greater than 20, there was a larger percentage of CD3 cells (44% vs. 29%; P = 0.015) expressing PD-1. When only patients with an APACHE II score greater than 20 were assessed, PD-1 expression on monocytes correlated positively with interleukin levels in the serum (r = 0.525, P = 0.05). Variability in the expression of PD-1 on leukocytes in critical surgical illness correlates with physiological dysfunction and suggests that PD-1 may be a valuable tool in the assessment of immune dysfunction following trauma or severe surgical insult.

摘要

程序性死亡受体 1(PD-1)是一种免疫系统的抑制蛋白受体,已在危重病动物模型以及创伤后和烧伤患者中显示上调。据信,PD-1 可能在外科危重病中观察到的免疫功能障碍中发挥作用。然而,尽管先前的研究已经将 PD-1 表达的变化与免疫细胞功能的改变相关联,但尚不清楚是否与临床状态存在相关性。因此,我们旨在描述 PD-1 在危重症创伤和外科患者中观察到的免疫功能障碍中的潜在作用。这是一项观察性队列研究。在一家三级护理/一级创伤中心的危重病和创伤外科重症监护病房患者中计算急性生理学和慢性健康评估 II(APACHE II)评分。在建立诊断和入住重症监护病房后的 24 小时内采集血液,以测量循环细胞因子水平以及循环细胞上的 PD-1 表达。主要观察指标包括白细胞上的 PD-1 表达与生理功能障碍(APACHE II)的关系,以及在生理功能障碍严重的患者中 PD-1 表达与白细胞介素 10 水平的相关性。从 90 名危重病外科患者中采集样本。在生理功能障碍严重(APACHE II>20)的患者中,表达 PD-1 的粒细胞(中位数,144 与 90 个细胞/μL;P=0.037)和单核细胞(中位数,12 与 6 个细胞/μL;P=0.022)数量增加。此外,在 APACHE II 评分大于 20 的患者中,表达 PD-1 的 CD3 细胞(44%与 29%;P=0.015)的比例更大。仅评估 APACHE II 评分大于 20 的患者时,单核细胞上的 PD-1 表达与血清中白细胞介素水平呈正相关(r=0.525,P=0.05)。在重症外科疾病中白细胞上 PD-1 的表达变异性与生理功能障碍相关,表明 PD-1 可能是评估创伤或严重外科损伤后免疫功能障碍的有价值工具。

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