P. Gessler et al., NEUTROPHIL RESPIRATORY BURST IN TERM AND PRETERM NEONATES WITHOUT SIGNS OF INFECTION AND IN THOSE WITH INCREASED LEVELS OF C-REACTIVE PROTEIN, Pediatric research, 39(5), 1996, pp. 843-848
Developmental immaturities in neonatal host defense predispose the neo
nates to an increased mortality rate during bacterial infections. Earl
y diagnosis is of great clinical importance, but, especially in neonat
es, is sometimes very difficult. The ability to generate reactive oxyg
en species, the so-called respiratory burst, is essential for neutroph
ils to kill infectious microorganisms. Therefore, changes of respirato
ry burst may reflect increased susceptibility of neonates to infection
s and may be useful for the early detection of infections. Superoxide
anion production was determined by a how cytometric method using dihyd
rorhodamine 123 (DHR) as an oxidative probe after priming of neutrophi
ls with PBS buffer (spontaneous burst), with N-formyl-methionyl-leucyl
-phenylalanine (fMLP), or with Escherichia coli. During the study peri
od, the spontaneous percentage of activated cells in whole blood as we
ll as the percentage of activated cells after stimulation with fMLP wa
s lower in adults (n = 100; PBS, 1.0 +/- 0.1%; fMLP, 8.3 +/- 0.9%) com
pared with neonates without signs of infection (n = 143). Among the la
tter, the percentage of activated cells (PBS and fMLP assay) varied wi
th respect to gestational age and hours of life: lowest values were me
asured in preterm newborns with gestational age less than 32 wk and be
tween 25 and 120 h of life. The same correlation to gestational age wa
s true for total neutrophil cell counts. In neonates with increased le
vels of C-reactive protein during the first 5 d of life (n = 43), the
percentages of activated cells after PBS and fMLP incubation were high
er than those of neonates without signs of infection. The relationship
of neutrophil respiratory burst and neutrophil cell counts to gestati
onal age might reflect at least in part a reason for the increased sus
ceptibility of neonates to infections. Furthermore, determination of r
espiratory burst may prove to be a new laboratory parameter of neonata
l infection.