Characterisation of the host inflammatory response to Staphylococcus epidermidis in neonatal whole blood

被引:35
作者
Haertel, C. [1 ]
Osthues, I. [1 ]
Rupp, J. [2 ]
Haase, B. [1 ]
Roeder, K. [3 ]
Goepel, W. [1 ]
Herting, E. [1 ]
Schultz, C. [1 ]
机构
[1] Med Univ Lubeck, Dept Paediat, D-23538 Lubeck, Germany
[2] Med Univ Lubeck, Inst Med Microbiol & Hyg, D-23538 Lubeck, Germany
[3] Med Univ Lubeck, Dept Obstet & Gynaecol, D-23538 Lubeck, Germany
来源
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION | 2008年 / 93卷 / 02期
关键词
D O I
10.1136/adc.2007.124685
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Coagulase-negative staphylocacci (CoNS) are the most prevalent pathogens causing late-onset sepsis, and gestational age is the most important risk factor for these infections. Objective: To characterise innate immune responses to S epidermidis by assessment of whole blood in vitro cytokine production in a large group of preterm and term infants. Results: The S epidermidis-induced in vitro production of proinflammatory cytokines such as intracytoplasmic interleukin (IL) 6 and tumour necrosis factor a in cord blood samples was found to be dependent on gestational age (R = 0.279, 95% Cl 010 to 0.44, p = 0.002; R = 0.251, 95% Cl 0.07 to 0.41, p = 0.005, respectively; n = 121). In contrast, the production of anti-inflammatory cytokines such as IL10 and transforming growth factor P was not associated with gestational age. When different stimulation strategies were compared, a strong correlation was noted for cytokine responses after lipopolysaccharide and S epidermidis exposure-that is, IL6 (R = 0.431, 95% Cl 0.29 to 0.55, p<0.001, n = 161) and IL10 (R = 0.332, 95% Cl 0.18 to 0.47, p<0.001, n = 161 In addition, a lower IL6 production was found in supernatants of whole blood cultures infected with a clinically isolated IcaABD-positive (biofilm production) strain compared with a control IcaABD-negative ATCC strain (p = 0.009). Conclusions: These in vitro data suggest that proinflammatory responses to S epidermidis are dependent on gestational age in preterm infants, whereas the counteracting anti-inflammatory response to S epidermidis may not be directly related to gestational age. Individual host factors may have a role as well as bacterial determinants, such as biofilm production. Further studies are encouraged to investigate the different aspects of innate immune responses to CoNS in vivo.
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收藏
页码:F140 / F145
页数:6
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