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慢性肺病高危婴儿肺流出液中补体过敏毒素C5a水平及地塞米松治疗的影响

Levels of complement anaphylatoxin C5a in pulmonary effluent fluid of infants at risk for chronic lung disease and effects of dexamethasone treatment.

作者信息

Groneck P, Oppermann M, Speer C P

机构信息

Department of Pediatrics, Children's Hospital of the City of Cologne, Germany.

出版信息

Pediatr Res. 1993 Nov;34(5):586-90. doi: 10.1203/00006450-199311000-00006.

DOI:10.1203/00006450-199311000-00006
PMID:8284093
Abstract

A number of studies have shown that increased numbers of neutrophils and macrophages are recruited into the airways during the development of chronic lung disease (CLD) in preterm infants. The objective of this study was to determine whether the anaphylatoxin C5a is detectable in tracheobronchial aspirate fluid of infants at risk for CLD and to evaluate the possible effects of dexamethasone (Dxm) treatment. C5a/C5a(des Arg) levels were determined by a sensitive ELISA based on a neoepitope-specific MAb. In a prospective study, 27 infants (birth weight 881 +/- 169 g, mean +/- SD) still on mechanical ventilation at d 10 postnatal age with fraction of inspired oxygen > or = 0.3 and/or peak inspiratory pressure > or = 16 cm H2O were randomly assigned to Dxm treatment at d 10 (n = 14) or d 16 (n = 13). Ten mechanically ventilated infants with no respiratory disease or who had recovered from respiratory distress syndrome did not meet these criteria on d 10 and served as a control group (birth weight 928 +/- 126 g). For the evaluation of Dxm therapy, the late treatment group was used as a control group for the early regimen. Compared with controls, C5a concentrations were higher in infants at risk for CLD on d 10 [median (25th-75th percentile): 2.40 (1.13-3.38) versus 0.82 (0.55-1.78) micrograms/L, p < 0.05].(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

多项研究表明,在早产儿慢性肺病(CLD)发展过程中,气道内募集的中性粒细胞和巨噬细胞数量会增加。本研究的目的是确定在有CLD风险的婴儿的气管支气管吸出液中是否可检测到过敏毒素C5a,并评估地塞米松(Dxm)治疗的可能效果。采用基于新表位特异性单克隆抗体的灵敏酶联免疫吸附测定法(ELISA)测定C5a/C5a(去精氨酸)水平。在一项前瞻性研究中,将27例出生后10天仍在机械通气、吸入氧分数≥0.3和/或吸气峰压≥16 cm H2O的婴儿(出生体重881±169 g,均值±标准差)随机分为10天(n = 14)或16天(n = 13)接受Dxm治疗两组。10例无呼吸系统疾病或已从呼吸窘迫综合征中恢复的机械通气婴儿在出生后10天不符合这些标准,作为对照组(出生体重928±126 g)。为评估Dxm治疗效果,将后期治疗组用作早期治疗方案的对照组。与对照组相比,有CLD风险的婴儿在出生后10天的C5a浓度更高[中位数(第25 - 75百分位数):2.40(1.13 - 3.38)对0.82(0.55 - 1.78)μg/L,p < 0.05]。(摘要截断于250字)

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