Elevated plasmatic level of soluble IL-7 receptor is associated with increased mortality in septic shock patients

被引:19
作者
Demaret, Julie [1 ,2 ,4 ]
Villars-Mechin, Astrid [1 ]
Lepape, Alain [2 ,3 ,4 ]
Plassais, Jonathan [4 ]
Vallin, Helene [3 ]
Malcus, Christophe [1 ]
Poitevin-Later, Francoise [1 ]
Monneret, Guillaume [1 ,2 ,4 ]
Venet, Fabienne [1 ,2 ,4 ]
机构
[1] Hosp Civils Lyon, Hop Edouard Herriot, Cellular Immunol Lab, F-69437 Lyon 03, France
[2] Univ Lyon 1, Hosp Civils Lyon, EAM 4174, F-69365 Lyon, France
[3] Hosp Civils Lyon, Lyon Sud Univ Hosp, Intens Care Units, Pierre Benite, France
[4] Hosp Civils Lyon, Hop Edouard Herriot, BioMerieux Joint Res Unit, F-69437 Lyon 03, France
关键词
IL-7; receptor; CD127; Septic shock; Mortality; Biomarker; INTERLEUKIN-7; RECEPTOR; T-CELLS; SEPSIS; EXPRESSION; MODEL; IMMUNOSUPPRESSION; DYSFUNCTIONS; MURINE; HIV;
D O I
10.1007/s00134-014-3346-0
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Adjunctive immunoadjuvant therapies are now proposed in the treatment of septic patients that develop immune dysfunctions. However, a prerequisite is to identify patients at high risk of death that would benefit from such therapy. Knowing that rhIL-7 is a putative candidate for septic shock treatment, we evaluated the association between increased plasmatic level of soluble CD127 (sCD127, IL-7 receptor alpha chain) and mortality after septic shock. sCD127 plasmatic level was measured in 70 septic shock patients sampled at day 1-2 (D1) and day 3-4 (D3) after the onset of shock and 41 healthy volunteers. Compared with survivors, non-survivors presented with significantly higher sCD127 concentrations at D1 and D3 (p < 0.001 and p = 0.002). At D1, the area under the receiver operating characteristic curve for sCD127 level association with mortality was 0.846 (p < 0.0001). Kaplan-Meier survival curves illustrated that mortality was significantly different after stratification based on D1 sCD127 level (log rank test, hazard ratio 9.10, p < 0.0001). This association was preserved in multivariate logistic regression analysis including clinical confounders (age, SAPS II and SOFA scores, odds ratio 12.71, p = 0.003). Importantly, patient stratification on both D1 sCD127 value and SAPS II score improved this predictive capacity (log rank test, p = 0.0001). Increased sCD127 plasmatic level enables the identification of a group of septic shock patients at high risk of death. After confirmation in a larger cohort, this biomarker may be of interest for patient stratification in future clinical trials.
引用
收藏
页码:1089 / 1096
页数:8
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