Reactive oxygen species released by blood phagocytes during the respir
atory burst may cause inflammatory tissue changes. We measured resting
and stimulated (opsonized zymosan or phorbol myristate acetate) chemi
luminescence of polymorphonuclear neutrophils on monocytes from 30 chi
ldren with mild, moderate or severe atopic dermatitis and normal contr
ols. Significant increases with respect to controls were observed in t
he phorbol myristate acetated-stimulated neutrophil responses in child
ren with severe disease and in the stimulated (opsonized zymosan or ph
orbol myristate acetate) monocyte responses in children with moderate
or severe disease. Although these changes do not appear to be an intri
nsic defect of oxidative metabolism, the increased release of reactive
oxygen species by these phagocytes may contribute to the pathogenesis
and maintenance of atopic dermatitis.