Yang Sung, Stepien David, Hanseman Dennis, Robinson Bryce, Goodman Michael D, Pritts Timothy A, Caldwell Charles C, Remick Daniel G, Lentsch Alex B
1Institute for Military Medicine, Division of Trauma and Critical Care, Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, OH. 2Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA.
Crit Care Med. 2014 Sep;42(9):2092-100. doi: 10.1097/CCM.0000000000000486.
Traumatic brain injury results in significant morbidity and mortality and is associated with infectious complications, particularly pneumonia. However, whether traumatic brain injury directly impacts the host response to pneumonia is unknown. The objective of this study was to determine the nature of the relationship between traumatic brain injury and the prevalence of pneumonia in trauma patients and investigate the mechanism of this relationship using a murine model of traumatic brain injury with pneumonia.
Data from the National Trauma Data Bank and a murine model of traumatic brain injury with postinjury pneumonia.
Academic medical centers in Cincinnati, OH, and Boston, MA.
PATIENTS/SUBJECTS: Trauma patients in the National Trauma Data Bank with a hospital length of stay greater than 2 days, age of at least 18 years at admission, and a blunt mechanism of injury. Subjects were female ICR mice 8-10 weeks old.
Administration of a substance P receptor antagonist in mice.
Pneumonia rates were measured in trauma patients before and after risk adjustment using propensity scoring. In addition, survival and pulmonary inflammation were measured in mice undergoing traumatic brain injury with or without pneumonia. After risk adjustment, we found that traumatic brain injury patients had significantly lower rates of pneumonia compared to blunt trauma patients without traumatic brain injury. A murine model of traumatic brain injury reproduced these clinical findings with mice subjected to traumatic brain injury demonstrating increased bacterial clearance and survival after induction of pneumonia. To determine the mechanisms responsible for this improvement, the substance P receptor was blocked in mice after traumatic brain injury. This treatment abrogated the traumatic brain injury-associated increases in bacterial clearance and survival.
The data demonstrate that patients with traumatic brain injury have lower rates of pneumonia compared to non-head-injured trauma patients and suggest that the mechanism of this effect occurs through traumatic brain injury-induced release of substance P, which improves innate immunity to decrease pneumonia.
创伤性脑损伤会导致严重的发病率和死亡率,并伴有感染性并发症,尤其是肺炎。然而,创伤性脑损伤是否直接影响宿主对肺炎的反应尚不清楚。本研究的目的是确定创伤性脑损伤与创伤患者肺炎患病率之间关系的本质,并使用创伤性脑损伤合并肺炎的小鼠模型研究这种关系的机制。
来自国家创伤数据库的数据以及创伤性脑损伤合并伤后肺炎的小鼠模型。
俄亥俄州辛辛那提市和马萨诸塞州波士顿市的学术医疗中心。
患者/受试者:国家创伤数据库中住院时间超过2天、入院时年龄至少18岁且为钝性损伤机制的创伤患者。受试者为8 - 10周龄的雌性ICR小鼠。
对小鼠给予P物质受体拮抗剂。
使用倾向评分在风险调整前后测量创伤患者的肺炎发生率。此外,测量有或无肺炎的创伤性脑损伤小鼠的存活率和肺部炎症。风险调整后,我们发现与无创伤性脑损伤的钝性创伤患者相比,创伤性脑损伤患者的肺炎发生率显著更低。创伤性脑损伤的小鼠模型再现了这些临床发现,遭受创伤性脑损伤的小鼠在诱发肺炎后显示出细菌清除增加和存活率提高。为了确定导致这种改善的机制,在创伤性脑损伤后的小鼠中阻断P物质受体。这种治疗消除了创伤性脑损伤相关的细菌清除增加和存活率提高。
数据表明,与非头部受伤的创伤患者相比,创伤性脑损伤患者的肺炎发生率更低,并表明这种效应的机制是通过创伤性脑损伤诱导释放P物质,从而改善先天免疫以降低肺炎发生率。