Neutrophil activation in preterm infants who have respiratory distress syndrome

被引:47
作者
Nupponen, I
Pesonen, E
Andersson, S
Mäkelä, A
Turunen, R
Kautiainen, H
Repo, H
机构
[1] Univ Helsinki, Haartman Inst, Dept Bacteriol & Immunol, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Anesthesiol, Helsinki, Finland
[3] Hosp Children & Adolescents, Helsinki, Finland
[4] Univ Helsinki, Dept Obstet & Gynecol, Helsinki, Finland
[5] Rheumatism Fdn Hosp, SF-18120 Heinola, Finland
[6] Univ Helsinki, Dept Med, Div Infect Dis, Helsinki, Finland
关键词
CD11b/CD18; C-reactive protein; neutrophil activation; preterm infant; respiratory distress syndrome; systemic inflammation;
D O I
10.1542/peds.110.1.36
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective. To study neutrophil activation in circulation as a sign of systemic inflammation in preterm infants with respiratory distress syndrome. Methods. The study comprised very low birth weight preterm infants who had respiratory distress syndrome and required intubation and mechanical ventilation (n = 51), 1-day-old preterm infants who had no need for mechanical ventilation (n = 12), term infants (n = 47), and adult volunteers (n = 25). Neutrophil surface expression of CD11b was quantified with flow cytometry. Results. In preterm infants with respiratory distress syndrome, neutrophil CD11b expression during the first day of life was higher than in cord blood (mean: 165 relative fluorescence units [RFU] [standard deviation [SD]: 53], n = 29 vs 83 RFU [SD: 21], n = 11; 95% confidence interval [CI] for difference: 59-106) or in preterm infants without mechanical ventilation (106 RFU [SD: 33], n = 12; 95% CI for difference: 17-90). CD11b expression decreased by age of 10 days. CD11b expression was lower in preterm cord than in term cord blood (95% CI for difference: 5-53). However, in preterm infants with respiratory distress syndrome aged 2 to 5 days, it was higher than in term infants of that age. Conclusions. The observations demonstrate an early transient postnatal neutrophil activation indicative of systemic inflammation that may contribute to the tissue injury in preterm infants with respiratory distress syndrome.
引用
收藏
页码:36 / 41
页数:6
相关论文
共 56 条
[41]   REDUCTION OF THE EDEMA OF ACUTE HYPEROXIC LUNG INJURY BY GRANULOCYTE DEPLETION [J].
SHASBY, DM ;
FOX, RB ;
HARADA, RN ;
REPINE, JE .
JOURNAL OF APPLIED PHYSIOLOGY, 1982, 52 (05) :1237-1244
[42]  
SHENNAN AT, 1988, PEDIATRICS, V82, P527
[43]   EXPRESSION OF THE COMPLEMENT RECEPTORS CR-1 AND CR3 AND THE TYPE-III FC-GAMMA RECEPTOR ON NEUTROPHILS FROM NEWBORN-INFANTS AND FROM FETUSES WITH RH DISEASE [J].
SMITH, JB ;
CAMPBELL, DE ;
LUDOMIRSKY, A ;
POLIN, RA ;
DOUGLAS, SD ;
GARTY, BZ ;
HARRIS, MC .
PEDIATRIC RESEARCH, 1990, 28 (02) :120-126
[44]   EOSINOPHILS AND NEUTROPHILS OF HUMAN NEONATES HAVE SIMILAR IMPAIRMENTS OF QUANTITATIVE UP-REGULATION OF MAC-1 (CD11B/CD18) EXPRESSION INVITRO [J].
SMITH, JB ;
KUNJUMMEN, RD ;
RAGHAVENDER, BH .
PEDIATRIC RESEARCH, 1991, 30 (04) :355-361
[45]  
SPEER CP, 1993, PEDIATRICS, V91, P794
[46]   PHAGOCYTIC FUNCTIONS AND TUMOR-NECROSIS-FACTOR SECRETION OF HUMAN MONOCYTES EXPOSED TO NATURAL PORCINE SURFACTANT (CUROSURF) [J].
SPEER, CP ;
GOTZE, B ;
CURSTEDT, T ;
ROBERTSON, B .
PEDIATRIC RESEARCH, 1991, 30 (01) :69-74
[47]   Markers of systemic inflammation predicting organ failure in community-acquired septic shock [J].
Takala, A ;
Jousela, I ;
Jansson, SE ;
Olkkola, KT ;
Takkunen, O ;
Orpana, A ;
Karonen, SL ;
Repo, H .
CLINICAL SCIENCE, 1999, 97 (05) :529-538
[48]   Systemic inflammatory response syndrome without systemic inflammation in acutely ill patients admitted to hospital in a medical emergency [J].
Takala, A ;
Jousela, I ;
Olkkola, KT ;
Jansson, SE ;
Leirisalo-Repo, M ;
Takkunen, O ;
Repo, H .
CLINICAL SCIENCE, 1999, 96 (03) :287-295
[49]   NEUTROPHILS AND THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
TATE, RM ;
REPINE, JE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1983, 128 (03) :552-559
[50]   DIVERSITY IN REGULATION OF ADHESION MOLECULES (MAC-1 AND L-SELECTIN) IN MONOCYTES AND NEUTROPHILS FROM NEONATES AND ADULTS [J].
TOROK, C ;
LUNDAHL, J ;
HED, J ;
LAGERCRANTZ, H .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1993, 68 (05) :561-565