N. Rebuck et al., NEUTROPHIL ADHESION MOLECULES IN TERM AND PREMATURE-INFANTS - NORMAL OR ENHANCED LEUKOCYTE INTEGRINS BUT DEFECTIVE L-SELECTIN EXPRESSION AND SHEDDING, Clinical and experimental immunology, 101(1), 1995, pp. 183-189
The functional deficits of neonatal neutrophils are well documented an
d are thought to contribute to the increased susceptibility of newborn
infants to infection. We measured the adhesion molecules L-selectin,
CD11a/CD18 and CD11b/CD18 on neutrophils from the cord blood of term(n
= 22) and premature (n = 32) infants using a whole blood method with
flow cytometry and quantitative bead standards to enumerate cell surfa
ce receptors. We also assayed plasma for the shed form of L-selectin (
sL-selectin). Our results suggested that L-selectin expression on term
infant neutrophils is lower than that on adult neutrophils (unstimula
ted and stimulated, both P < 0.001), but that stimulated premature inf
ant cells express higher L-selectin than term infants (P < 0.05); it i
s possible that this deficiency is caused by physiological changes occ
urring around the normal time of parturition. We observed reduced sl-s
electin in term infants (P < 0.001) compared with adults, and even low
er concentrations in premature infants (P < 0.001). The sL-selectin co
ncentrations in plasma may be a reflection of granulopoiesis, which ma
y be reduced in premature infants. Our results showed increased restin
g neonatal neutrophil expression of CD11b/CD18 compared with adults, a
nd the absence of any neonatal deficit of the ability to up-regulate C
D11b/CD18 expression on stimulation. These findings are contrary to pr
evious reports. Further studies suggested that the isolation procedure
s used in previous reports reduces the capability of the cells to resp
ond to a formyl methionine leucine phenylalanine (fMLP) stimulus. This
effect is more marked in neonatal neutrophils, suggesting that the pr
eviously reported deficiency is in fact due to the isolation technique
s used rather than the cells' innate ability to up-regulate CD11b/CD18
expression. The results of our study lead us to propose that the adhe
sive function of neonatal neutrophils may be less defective than previ
ously thought.