Persistently Elevated Soluble Triggering Receptor Expressed on Myeloid Cells 1 and Decreased Monocyte Human Leucocyte Antigen DR Expression Are Associated With Nosocomial Infections in Septic Shock Patients.

Matthieu Venet, Frank Bidar, Marc Derive, Benjamin Delwarde, Céline Monard, Baptiste Hengy, Lucie Jolly, Thomas Rimmelé, Anne-Claire Lukaszewicz, Guillaume Monneret, Fabienne Venet
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Abstract

Sepsis-acquired immunosuppression may play a major role in patients' prognosis through increased risk of secondary infections. Triggering receptor expressed on myeloid cells 1 (TREM-1) is an innate immune receptor involved in cellular activation. Its soluble form (sTREM-1) has been described as a robust marker of mortality in sepsis. The objective of this study was to evaluate its association with the occurrence of nosocomial infections alone or in combination with human leucocyte antigen-DR on monocytes (mHLA-DR).

Design: Observational study.

Setting: University Hospital in France.

Patients: One hundred sixteen adult septic shock patients as a post hoc study from the IMMUNOSEPSIS cohort (NCT04067674).

Interventions: None.

Measurements and main results: Plasma sTREM-1 and monocyte HLA-DR were measured at day 1 or 2 (D1/D2), D3/D4, and D6/D8 after admission. Associations with nosocomial infection were evaluated through multivariable analyses. At D6/D8, both markers were combined, and association with increased risk of nosocomial infection was evaluated in the subgroup of patients with most deregulated markers in a multivariable analysis with death as a competing risk. Significantly decreased mHLA-DR at D6/D8 and increased sTREM-1 concentrations were measured at all time points in nonsurvivors compared with survivors. Decreased mHLA-DR at D6/D8 was significantly associated with increased risk of secondary infections after adjustment for clinical parameters with a subdistribution hazard ratio of 3.61 (95% CI, 1.39-9.34; p = 0.008). At D6/D8, patients with persistently high sTREM-1 and decreased mHLA-DR presented with a significantly increased risk of infection (60%) compared with other patients (15.7%). This association remained significant in the multivariable model (subdistribution hazard ratio [95% CI], 4.65 [1.98-10.9]; p < 0.001).

Conclusions: In addition to its prognostic interest on mortality, sTREM-1, when combined with mHLA-DR, may help to better identify immunosuppressed patients at risk of nosocomial infections.

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粒细胞可溶性触发受体1表达持续升高和单核细胞人白细胞抗原DR表达下降与感染性休克患者院内感染有关
脓毒症获得性免疫抑制可能通过增加继发感染的风险在患者预后中起主要作用。髓样细胞上表达的触发受体1 (TREM-1)是一种参与细胞活化的先天免疫受体。它的可溶性形式(sTREM-1)被认为是脓毒症死亡率的一个强有力的标志。本研究的目的是评估其单独或联合人白细胞抗原-单核细胞dr (mHLA-DR)与院内感染发生的关系。设计:观察性研究。地点:法国大学医院。患者:来自免疫败血症队列(NCT04067674)的116名成人感染性休克患者作为事后研究。干预措施:没有。入院后第1、2天(D1/D2)、D3/D4、D6/D8分别测定血浆sTREM-1和单核细胞HLA-DR。通过多变量分析评估与医院感染的关系。在D6/D8时,两种标记物联合使用,并在多变量分析中以死亡作为竞争风险,在标记物最不受控制的患者亚组中评估与医院感染风险增加的关联。与幸存者相比,非幸存者在D6/D8时的mHLA-DR显著降低,在所有时间点的sTREM-1浓度均升高。调整临床参数后,D6/D8时mHLA-DR降低与继发感染风险增加显著相关,亚分布风险比为3.61 (95% CI, 1.39-9.34;P = 0.008)。在D6/D8时,持续高sTREM-1和mHLA-DR降低的患者与其他患者(15.7%)相比,感染风险显著增加(60%)。这种关联在多变量模型中仍然显著(亚分布风险比[95% CI], 4.65 [1.98-10.9];P < 0.001)。结论:除了对死亡率的预后感兴趣外,sTREM-1与mHLA-DR联合使用可能有助于更好地识别有医院感染风险的免疫抑制患者。
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