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本文引用的文献

1
An adequately robust early TNF-alpha response is a hallmark of survival following trauma/hemorrhage.在创伤/出血后,早期 TNF-α 反应足够强烈是存活的标志。
PLoS One. 2009 Dec 22;4(12):e8406. doi: 10.1371/journal.pone.0008406.
2
Early cytokine production risk stratifies trauma patients for multiple organ failure.早期细胞因子产生可对创伤患者发生多器官功能衰竭进行风险分层。
J Am Coll Surg. 2009 Sep;209(3):320-31. doi: 10.1016/j.jamcollsurg.2009.05.002. Epub 2009 Jun 28.
3
Isolated closed minor-muscle injury of the lower leg did not cause an obvious systemic immune response.小腿孤立性小肌肉闭合性损伤不会引起明显的全身免疫反应。
Inflamm Res. 2010 Feb;59(2):141-9. doi: 10.1007/s00011-009-0081-z. Epub 2009 Aug 26.
4
Invited review: deterioration of the immune system after trauma: signals and cellular mechanisms.特邀综述:创伤后免疫系统的衰退:信号与细胞机制
Innate Immun. 2008 Dec;14(6):333-44. doi: 10.1177/1753425908100016.
5
Early immunologic responses to trauma in the emergency department patients with major injuries.急诊科重伤患者对创伤的早期免疫反应。
Resuscitation. 2009 Jan;80(1):83-8. doi: 10.1016/j.resuscitation.2008.09.012. Epub 2008 Nov 7.
6
Effect of interleukin-15 on depressed splenic dendritic cell functions following trauma-hemorrhage.白细胞介素-15对创伤性出血后脾脏树突状细胞功能抑制的影响。
Am J Physiol Cell Physiol. 2009 Jan;296(1):C124-30. doi: 10.1152/ajpcell.00447.2008. Epub 2008 Nov 5.
7
Elevated systemic interleukin-18 in multiple injured patients is not related to clinical outcome.多发伤患者全身白细胞介素-18升高与临床结局无关。
J Interferon Cytokine Res. 2008 Dec;28(12):741-7. doi: 10.1089/jir.2008.0029.
8
Hemoglobin-based oxygen carrying compound-201 as salvage therapy for severe neuro- and polytrauma (Injury Severity Score = 27-41).基于血红蛋白的携氧化合物-201作为严重神经创伤和多发伤(损伤严重度评分=27-41)的挽救治疗手段。
Crit Care Med. 2008 Oct;36(10):2838-48. doi: 10.1097/CCM.0b013e318186f6b3.
9
Bench-to-bedside review: latest results in hemorrhagic shock.从实验台到病床的综述:失血性休克的最新研究成果
Crit Care. 2008;12(4):218. doi: 10.1186/cc6919. Epub 2008 Jul 10.
10
Gender differences in trauma theory vs. practice: Comments on "Mechanism of estrogen-mediated intestinal protection following trauma-hemorrhage: p38 MAPK-dependent upregulation of HO-1" by Hsu JT et al.创伤理论与实践中的性别差异:评许JT等人的《创伤性出血后雌激素介导的肠道保护机制:p38丝裂原活化蛋白激酶依赖性上调血红素加氧酶-1》
Am J Physiol Regul Integr Comp Physiol. 2008 Jun;294(6):R1822-4. doi: 10.1152/ajpregu.90301.2008. Epub 2008 Apr 16.

猪创伤和失血性休克模型中细胞因子和热休克蛋白的全身释放*。

Systemic release of cytokines and heat shock proteins in porcine models of polytrauma and hemorrhage*.

机构信息

Burn and Shock Trauma Institute, Loyola University Chicago, Stritch School of Medicine, Maywood, IL, USA.

出版信息

Crit Care Med. 2012 Mar;40(3):876-85. doi: 10.1097/CCM.0b013e318232e314.

DOI:10.1097/CCM.0b013e318232e314
PMID:21983369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3383056/
Abstract

OBJECTIVE

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.

DESIGN

Prospective observational study.

SETTING

Research laboratory.

SUBJECTS

Twenty-one Yorkshire pigs.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

设计

前瞻性观察性研究。

地点

研究实验室。

对象

21 头约克郡猪。

干预

无。

测量和主要结果

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。

结论

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。