Early elevation of soluble CD14 may help identify trauma patients at high risk for infection

被引:29
作者
Carrillo, EH [1 ]
Gordon, L
Goode, E
Davis, E
Polk, HC
机构
[1] Univ Louisville, Sch Med, Dept Surg, Louisville, KY 40292 USA
[2] Univ Louisville Hosp, Trauma Program Surg, Louisville, KY USA
[3] Mary & Mason Rudd Surg Teaching Endowment, Louisville, KY USA
[4] Prince Inst Surg Res, Louisville, KY USA
来源
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE | 2001年 / 50卷 / 05期
关键词
CD14; trauma; sepsis; infection;
D O I
10.1097/00005373-200105000-00006
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Elevated levels of soluble CD14 (sCD14) have been implicated in both gram-positive and gram-negative sepsis, and it has been associated with high mortality in trauma patients who become infected, Methods: Eleven healthy volunteers and 25 adult trauma patients with multiple:injuries and a mean Injury Severity Score of 32 participated, Whole blood was obtained at intervals. Immunohistochemistry,was used to quantify membrane CD14 (mCD14), by flow cytometry and plasma levels of sCD14 by enzyme-linked immunosorbent assay. Analysis of variance and Student's t test with Mann-Whitney posttest were used to determine significance at p < 0.05. Results: On posttrauma day 1, sCD14 was significantly different in the plasma of infected patients compared with normal controls (7.16 <plus/minus> 1.87 mug/mL vs. 4.4 +/- 0.92 mug/mL, p < 0.01), but not significantly different from noninfected patients. The percentage of monocytes expressing mCD14 in trauma patients did not differentiate them from normal controls; however, mCD14 receptor density did demonstrate significance in septic trauma patients (n = 15) versus normal controls on posttrauma day 3 (p = 0.0065). Conclusion: On the basis of our data, mCD14 did not differentiate infected and noninfected trauma patients, although trauma in general reduced mCD14 and elevated sCD14. Interestingly, 100% of patients who exceeded plasma levels of 8 mug/mL of sCD14 on day 1 after injury developed infections. Therefore, early high expressers of sCD14 mag. be at higher risk for infectious complications after trauma.
引用
收藏
页码:810 / 815
页数:6
相关论文
共 39 条
[1]   MULTIPLE ORGAN FAILURE, MULTIPLE ORGAN DYSFUNCTION SYNDROME, AND, THE SYSTEMIC INFLAMMATORY RESPONSE SYNDROME - WHERE DO WE STAND [J].
BAUE, AE .
SHOCK, 1994, 2 (06) :385-397
[2]  
BAZIL V, 1991, J IMMUNOL, V147, P1567
[3]   MODULATION OF THE ENDOTOXIN RECEPTOR (CD14) IN SEPTIC PATIENTS [J].
BIRKENMAIER, C ;
HONG, YS ;
HORN, JK .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1992, 32 (04) :473-479
[4]   Serum levels of CD14 in neonatal sepsis by Gram-positive and Gram-negative bacteria [J].
Blanco, A ;
Solis, G ;
Arranz, E ;
Coto, GD ;
Ramos, A ;
Telleria, J .
ACTA PAEDIATRICA, 1996, 85 (06) :728-732
[5]   Sepsis and septic complications in the surgical patient: Who is at risk? [J].
Cheadle, WG ;
MercerJones, M ;
Heinzelmann, M ;
Polk, HC .
SHOCK, 1996, 6 :S6-S9
[6]   Secretory leukocyte protease inhibitor interferes with uptake of lipopolysaccharide by macrophages [J].
Ding, A ;
Thieblemont, N ;
Zhu, J ;
Jin, FY ;
Zhang, J ;
Wright, S .
INFECTION AND IMMUNITY, 1999, 67 (09) :4485-4489
[7]   THE 2 SOLUBLE FORMS OF THE LIPOPOLYSACCHARIDE RECEPTOR, CD14 - CHARACTERIZATION AND RELEASE BY NORMAL HUMAN MONOCYTES [J].
DURIEUX, JJ ;
VITA, N ;
POPESCU, O ;
GUETTE, F ;
CALZADAWACK, J ;
MUNKER, R ;
SCHMIDT, RE ;
LUPKER, J ;
FERRARA, P ;
ZIEGLERHEITBROCK, HWL ;
LABETA, MO .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2006-2012
[8]   Lactoferrin inhibits the endotoxin interaction with CD14 by competition with the lipopolysaccharide-binding protein [J].
Elass-Rochard, E ;
Legrand, D ;
Salmon, V ;
Roseanu, A ;
Trif, M ;
Tobias, PS ;
Mazurier, J ;
Spik, G .
INFECTION AND IMMUNITY, 1998, 66 (02) :486-491
[9]  
ERTEL W, 1993, SURGERY, V114, P243
[10]   LPS-binding proteins and receptors [J].
Fenton, MJ ;
Golenbock, DT .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 64 (01) :25-32