Hallwirth Ulrike, Pomberger Gerhard, Zaknun Daniela, Szepfalusi Zsolt, Horcher Ernst, Pollak Arnold, Roth Erich, Spittler Andreas
Division of Pediatric Surgery, Department of Surgery, University Medical School of Vienna, AKH Waehringer Guertel 18-20, 1090 Vienna, Austria.
Early Hum Dev. 2002 Apr;67(1-2):1-9. doi: 10.1016/s0378-3782(01)00245-6.
Septic complications lead to a high mortality rate in very low birthweight infants (VLBWI). Therefore, prognostic markers for the development of sepsis attach importance to start an efficient therapy as early as possible.
Functional and phenotypical variables of blood monocytes in the cord and peripheral blood were investigated to evaluate the parameters for predicting early-onset and late-onset sepsis (nosocomial infections).
In a prospective study, 25 VLBWI were investigated.
In the cord blood taken immediately after birth, the capacity of the monocytes to phagocytose non-opsonized E. coli bacteria by flow cytometry and the ex-vivo production of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta and IL-6 (enzyme-linked immunoassay (ELISA)) after lipopolysaccharide (LPS) stimulation were measured. At the third day, the HLA-DR expression on the monocytes (flow cytometry) and the LPS-induced cytokine production were measured from the peripheral blood.
Five VLBWI already developed early septic complications after 24-72 h, while the other three infants had late-onset sepsis 10-18 days after birth. The prognostic significance for early-onset sepsis was highest for the decreased monocyte phagocytic capacity (sensitivity and specificity: 100%) and for the LPS-induced formation of TNF-alpha and IL-1 beta in cord blood. Moreover, in septic VLBWI, the HLA-DR expression on the monocytes was lowered on day 3 after birth. The prognostic significance for late-onset sepsis was highest for TNF-alpha and IL-1 beta levels in the peripheral blood on the third day after birth.
The determination of phagocytosis in the cord blood seems to be a reliable parameter for predicting early-onset sepsis and offers the possibility for a forward start of an antibiotic therapy.
脓毒症并发症导致极低出生体重儿(VLBWI)死亡率很高。因此,脓毒症发生的预后标志物对于尽早开始有效治疗至关重要。
研究脐带血和外周血中血液单核细胞的功能及表型变量,以评估预测早发型和晚发型脓毒症(医院感染)的参数。
在一项前瞻性研究中,对25例极低出生体重儿进行了调查。
在出生后立即采集的脐带血中,通过流式细胞术检测单核细胞吞噬未调理的大肠杆菌的能力,并在脂多糖(LPS)刺激后通过酶联免疫吸附测定(ELISA)检测肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和IL-6的体外产生情况。在第三天,从外周血中检测单核细胞上的HLA-DR表达(流式细胞术)和LPS诱导的细胞因子产生情况。
5例极低出生体重儿在24 - 72小时后已出现早期脓毒症并发症,而另外3例婴儿在出生后10 - 18天发生了晚发型脓毒症。对于早发型脓毒症,单核细胞吞噬能力降低(敏感性和特异性:100%)以及脐带血中LPS诱导的TNF-α和IL-1β形成具有最高的预后意义。此外,在发生脓毒症的极低出生体重儿中,出生后第3天单核细胞上的HLA-DR表达降低。对于晚发型脓毒症,出生后第三天外周血中TNF-α和IL-1β水平具有最高的预后意义。
脐带血中吞噬作用的测定似乎是预测早发型脓毒症的可靠参数,并为提前开始抗生素治疗提供了可能性。