Potential role of interleukin-1 in the development of bronchopulmonary dysplasia

被引:58
作者
Rindfleisch, MS
Hasday, JD
Taciak, V
Broderick, K
Viscardi, RM
机构
[1] UNIV MARYLAND, SCH MED, DEPT PEDIAT, DIV NEONATOL, BALTIMORE, MD 21201 USA
[2] UNIV MARYLAND, SCH MED, DEPT MED, DIV PULM & CRIT CARE MED, BALTIMORE, MD 21201 USA
[3] ST AGNES HOSP, DEPT PEDIAT, DIV NEONATOL, BALTIMORE, MD USA
关键词
D O I
10.1089/jir.1996.16.365
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increased activities of inflammatory mediators unopposed by their inhibitors contribute to chronic lung injury and impaired healing in BPD, The deleterious effects of IL-1 beta, a cytokine involved in inflammation and host defense, are blocked by IL-1 receptor antagonist (IL-1Ra), We proposed that an imbalance of IL-1 beta and its inhibitors may contribute to the development of BPD, To determine the relative antigen concentrations of IL-1 beta and IL-1Ra and functional IL-1 activity in lung lavage of infants at risk for BPD, lung lavage was serially obtained from 1 to 28 days from 17 infants with evolving BPD, 13 infants with self-limited RDS, and 6 controls ventilated for nonpulmonary reasons, Overall, there was a high correlation between IL-1 beta antigen concentration and IL-1 activity (r = 0.82, p = 0.0001), There were no significant differences among the groups for lung lavage variables on day 1, However, in infants who developed BPD, IL-1 beta antigen concentration and IL-1 activity increased 16- and 61-fold, respectively, during the first week, IL-1Ra remained relatively unchanged during the first month, IL-1 beta/IL-1Ra antigen ratio was significantly higher on days 5 (median 0.024) and 7 (median 0.025) compared with day 1 (median 0.004), p < 0.05, These results suggest that a relative imbalance of IL-1 beta and IL-1Ra may contribute to prolonged inflammation in BPD.
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页码:365 / 373
页数:9
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