Bacterial and fungal sepsis are major causes of morbidity and mortality in
the newborn. Multiple factors contribute to this increased susceptibility t
o infection, including quantitative and qualitative neutrophil defects, wit
h a reduction in neutrophil number and function. Neutropenia in the newborn
may occur in association with sepsis and has a poor prognosis. In addition
to antibiotic therapy and supportive care, granulocyte colony-stimulating
factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF
) have been used to reduce morbidity and mortality. Granulocyte CSF is the
physiological regulator of neutrophil production and function. Administrati
on of G-CSF results in increased neutrophil production and counts and impro
ved neutrophil function. Several studies of animal and human newborns havin
g neutropenia or suspected sepsis investigated the use of G-CSF and GM-CSF
to elevate neutrophil counts and reduce morbidity and mortality in this pop
ulation. Results of small clinical trials using G-CSF and GM-CSF in very lo
w-birth-weight infants having neutropenia show increased neutrophil counts
and a reduced incidence of sepsis during the neonatal period. Despite these
promising early results, further studies of the safety and efficacy of G-C
SF and GM-CSF administration in neonates are required before their routine
use can be recommended as either prophylaxis or treatment for neonatal seps
is.