Burn and Shock Trauma Institute, Loyola University Chicago, Stritch School of Medicine, Maywood, IL, USA.
Crit Care Med. 2012 Mar;40(3):876-85. doi: 10.1097/CCM.0b013e318232e314.
To define systemic release kinetics of a panel of cytokines and heat shock proteins in porcine polytrauma/hemorrhage models and to evaluate whether they could be useful as early trauma biomarkers.
Prospective observational study.
Research laboratory.
Twenty-one Yorkshire pigs.
None.
Pigs underwent polytrauma (femur fractures/lung contusion, P), hemorrhage (mean arterial pressure 25-30 mm Hg, H), polytrauma plus hemorrhage (P/H), or sham procedure (S). Plasma was obtained at baseline, in 5- to 15-min intervals during a 60-min shock period without intervention, and in 60- to 120-min intervals during fluid resuscitation for up to 300 min. Plasma was assayed for interleukin-1β, interleukin-4, interleukin-5, interleukin-6, interleukin-8, interleukin-10, interleukin-12/interleukin-23p40, interleukin-13, interleukin-17, interleukin-18, interferonγ, transforming growth factor-β, tumor necrosis factor-α, heat shock protein 40, heat shock protein 70, and heat shock protein 90 by enzyme-linked immunosorbent assay. All animals after S, P, and H survived (n = 5/group). Three of six animals after P/H died. Interleukin-10 increased during shock after P and this increase was attenuated after H. Tumor necrosis factor-α increased during the shock period after P, H, and also after S. P/H abolished the systemic interleukin-10 and tumor necrosis factor-α release and resulted in 20% to 30% increased levels of interleukin-6 during shock. As fluid resuscitation was initiated, tumor necrosis factor-α and interleukin-10 levels decreased after P, H, and P/H; heat shock protein 70 increased after P; and interleukin-6 levels remained elevated after P/H and also increased after P and S.
Differential regulation of the systemic cytokine release after polytrauma and/or hemorrhage, in combination with the effects of resuscitation, can explain the variability and inconsistent association of systemic cytokine/heat shock protein levels with clinical variables in trauma patients. Insults of major severity (P/H) partially suppress the systemic inflammatory response. The plasma concentrations of the measured cytokines/heat shock proteins do not reflect injury severity or physiological changes in porcine trauma models and are unlikely to be able to serve as useful trauma biomarkers in patients.
定义猪创伤/失血模型中细胞因子和热休克蛋白的全身释放动力学,并评估它们是否可用作早期创伤生物标志物。
前瞻性观察性研究。
研究实验室。
21 头约克郡猪。
无。
猪接受多发伤(股骨骨折/肺挫伤,P)、失血(平均动脉压 25-30mmHg,H)、多发伤加失血(P/H)或假手术(S)。在无干预的 60 分钟休克期内,每隔 5-15 分钟取一次血样,在液体复苏的 60-120 分钟间隔内取一次血样,直至 300 分钟。通过酶联免疫吸附试验检测血浆中白细胞介素-1β、白细胞介素-4、白细胞介素-5、白细胞介素-6、白细胞介素-8、白细胞介素-10、白细胞介素-12/白细胞介素-23p40、白细胞介素-13、白细胞介素-17、白细胞介素-18、干扰素γ、转化生长因子-β、肿瘤坏死因子-α、热休克蛋白 40、热休克蛋白 70 和热休克蛋白 90。S、P 和 H 后所有动物存活(每组 5 只)。P/H 后有 6 只动物中的 3 只死亡。P 和 H 后休克期间白细胞介素-10 增加,而 H 后这种增加被减弱。P、H 和 S 后休克期间肿瘤坏死因子-α增加。P/H 消除了全身白细胞介素-10 和肿瘤坏死因子-α释放,并导致休克期间白细胞介素-6 水平升高 20%-30%。液体复苏开始后,P、H 和 P/H 后肿瘤坏死因子-α和白细胞介素-10 水平下降;P 后热休克蛋白 70 增加;P/H 后白细胞介素-6 水平持续升高,P 和 S 后也升高。
多发伤和/或失血后全身细胞因子释放的差异调节,结合复苏的影响,可以解释创伤患者全身细胞因子/热休克蛋白水平与临床变量的可变性和不一致性。严重程度较大的损伤(P/H)部分抑制全身炎症反应。所测量的细胞因子/热休克蛋白的血浆浓度不能反映猪创伤模型中的损伤严重程度或生理变化,不太可能作为患者有用的创伤生物标志物。