Abstract

Newborns (N) have an increased susceptibility to infection. Because of conflicting previous data on the functional capabilities of their PMN metabolic, phagocytic and bactericidal activities of normal full term N were studied and compared to normal adult controls. Phagocytosis of 14C S. aureus 502A at 20 min. and myeloperoxidase mediated protein iodination at 60 min. were not depressed. Resting 14C-1-glucose oxidation was equivalent, however 60 min. after phagocytosis of yeast N-PMN exhibited significant depressions in activity when compared to the controls (783±132 cpm 14CO2/1×106 PMN v.s. 1545±179, P<0.01). This was paralleled by reduced rates of O2 consumption by N-PMN after 10 min. of phagocytosis (10-15 min. 2.89±0.19 μmoles/15×106 PMN/min. v.s. 3.66±0.20, P<0.02; 15-20 min.;1.76±0.11 v.s. 2.30±0.11, P<0.02), while initial rates were similar. These defects may reflect decreased H2O2 production. These observations were paralleled by a mild but significant reduction in the killing of S. aureus 502A by N-PMN evident only on prolonged incubation (60 min,;92.8% killed v.s. 95.7%, P<0.02, 120 min.;95.1% v.s. 97.2%, P<0.05). These studies suggest that N-PMN have diminished H2O2 production reflected in a mild impairment of bactericidal activity. When coupled with previously documented opsonic and chemotactic defects these findings may have pathogenetic significance in the increased susceptibility of the N to infection.

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