To evaluate the hypothesis that the proinflammatory cytokines IL-1, IL-6, and tumor necrosis factor-α might be the link between prenatal intrauterine infection (IUI) and neonatal brain damage, the authors review the relevant epidemiologic and cytokine literature. Maternal IUI appears to increase the risk of preterm delivery, which in turn is associated with an increased risk of intraventricular hemorrhage, neonatal white matter damage, and subsequent cerebral palsy. IL-1, IL-6, and TNF-α have been found associated with IUI, preterm birth, neonatal infections, and neonatal brain damage. Unifying models not only postulate the presence of cytokines in the three relevant maternal/fetal compartments (uterus, fetal circulation, and fetal brain) and the ability of the cytokines to cross boundaries (placenta and blood-brain barrier) between these compartments, but also postulate how proinflammatory cytokines might lead to IVH and neonatal white matter damage during prenatal maternal infection. Interrupting the proinflammatory cytokine cascade might prevent later disability in those born near the end of the second trimester.
Abbreviations: BBB, blood-brain barrier; IUI, intrauterine infection; IVH, intraventricular hemorrhage;PVL, periventricular leukomalacia; TNF, tumor necrosis factor; VLBW, very low birth weight