Elevated gene expression of interleukin-8 in cord blood is a sensitive marker for neonatal infection

被引:39
作者
Berner, R
Tüxen, B
Clad, A
Forster, J
Brandis, M
机构
[1] Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany
[2] Univ Freiburg, Hosp Obstet & Gynecol, D-79106 Freiburg, Germany
关键词
neonatal sepsis; cytokines; mRNA; reverse transcriptase-polymerase chain reaction;
D O I
10.1007/s004310050051
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Bacterial infection is a major cause of neonatal morbidity and mortality. Early diagnosis is essential for a successful treatment and outcome. Cytokine plasma levels are suggested to be sensitive parameters for the diagnosis of neonatal sepsis. The aim of this study was to assess cytokine mRNA expression in cord blood cells as a marker for neonatal infection. In a prospective study, cord blood samples of neonates with septic bacterial infection were analyzed qualitatively and semiquantitatively by reverse transcriptase-polymerase chain reaction (RT-PCR) for mRNA expression of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6, IL-8, as well as for IL-8 cord plasma levels. Results were compared to those of non-septic neonates. A method was used requiring only a microvolume (25 mu l or less) of cord blood. Cord plasma levels of IL-8 were significantly elevated in septic infants (n = 9) when compared to infants with not confirmed sepsis (n = 22) and healthy infants that served as controls (n = 68) (median 1,686 vs 262.7 vs 33.1 pg/ml, P < 0.001). The presence of IL-6 and TNF-alpha gene expression was observed more frequently in septic than in non-septic patients; sensitivity, however, reached only 56 and 67%, respectively. When using a semiquantitative approach for analyzing IL-8 mRNA levels, a high sensitivity (86%) and specificity (96%) for the detection of sepsis was achieved. A new method for the early diagnosis of neonatal infection is described measuring cytokine mRNA in neonatal cord blood cells. With this molecular approach only a microvolume of blood is required for analysis.
引用
收藏
页码:205 / 210
页数:6
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