Hospices Civils de Lyon, Service de réanimation, Hôpital Edouard Herriot, 5 place d'Arsonval-69437 Lyon Cedex 03, France.
Crit Care. 2010;14(6):R208. doi: 10.1186/cc9331. Epub 2010 Nov 19.
Major trauma is characterized by an overwhelming pro-inflammatory response and an accompanying anti-inflammatory response that lead to a state of immunosuppression, as observed after septic shock. Diminished monocyte Human Leukocyte Antigen DR (mHLA-DR) is a reliable marker of monocyte dysfunction and immunosuppression. The main objective of this study was to determine the relation between mHLA-DR expression in severe trauma patients and the development of sepsis.
We conducted a prospective observational study over 23 months in a trauma intensive care unit at a university hospital. Patients with an Injury Severity Score (ISS) over 25 and age over 18 were included. mHLA-DR was assessed by flow cytometry protocol according to standardized protocol. Mann-Whitney U-test for continuous non-parametric variables, independent paired t test for continuous parametric variables and chi-square test for categorical data were used.
mHLA-DR was measured three times a week during the first 14 days. One hundred five consecutive severely injured patients were monitored (ISS 38 ± 17, SAPS II 37 ± 16). Thirty-seven patients (35%) developed sepsis over the 14 days post-trauma. At days 1-2, mHLA-DR was diminished in the whole patient population, with no difference with the development of sepsis. At days 3-4, a highly significant difference appeared between septic and non-septic patients. Non- septic patients showed an increase in mHLA-DR levels, whereas septic patients did not (13,723 ± 7,766 versus 9,271 ± 6,029 antibodies per cell, p = .004). Most importantly, multivariate logistic regression analysis, after adjustment for usual clinical confounders (adjusted OR 5.41, 95% CI 1.42-20.52), revealed that a slope of mHLA-DR expression between days1-2 and days 3-4 below 1.2 remained associated with the development of sepsis.
Major trauma induced an immunosuppression, characterized by a decrease in mHLA-DR expression. Importantly, after multivariate regression logistic analysis, persistent decreased expression was assessed to be in relation with the development of sepsis. This is the first study in trauma patients showing a link between the lack of immune recovery and the development of sepsis on the basis of the standardized protocol. Monitoring immune function by mHLA-DR measurement could be useful to identify trauma patients at a high risk of infection.
严重创伤的特征是炎症反应过度和随之而来的抗炎反应,导致免疫抑制状态,类似于败血症休克后的状态。单核细胞人类白细胞抗原 DR(mHLA-DR)减少是单核细胞功能障碍和免疫抑制的可靠标志物。本研究的主要目的是确定严重创伤患者 mHLA-DR 表达与败血症发展之间的关系。
我们在一家大学医院的创伤重症监护病房进行了一项为期 23 个月的前瞻性观察研究。纳入损伤严重程度评分(ISS)>25 岁和年龄>18 岁的患者。通过流式细胞术方案按标准化方案评估 mHLA-DR。连续非参数变量采用 Mann-Whitney U 检验,连续参数变量采用独立配对 t 检验,分类数据采用卡方检验。
在最初的 14 天内,每周测量 mHLA-DR 三次。监测了 105 例连续严重创伤患者(ISS 38 ± 17,SAPS II 37 ± 16)。创伤后 14 天内,37 例(35%)患者发生败血症。在第 1-2 天,整个患者人群的 mHLA-DR 减少,与败血症的发展没有差异。在第 3-4 天,败血症和非败血症患者之间出现了非常显著的差异。非败血症患者的 mHLA-DR 水平升高,而败血症患者则没有(每个细胞 13723 ± 7766 与 9271 ± 6029 抗体,p=.004)。最重要的是,在调整了通常的临床混杂因素(调整后的 OR 5.41,95%CI 1.42-20.52)后,多变量逻辑回归分析显示,mHLA-DR 表达在第 1-2 天和第 3-4 天之间的斜率低于 1.2 与败血症的发展仍有关联。
严重创伤引起免疫抑制,表现为 mHLA-DR 表达减少。重要的是,经过多变量回归逻辑分析,持续的表达下降与败血症的发展有关。这是第一项在创伤患者中进行的研究,根据标准化方案显示免疫恢复缺乏与败血症的发展之间存在联系。通过 mHLA-DR 测量监测免疫功能可能有助于识别感染风险较高的创伤患者。