Abstract
The concept of preventing neonatal infections by immunizing pregnant women has been appreciated for over a century and has been studied extensively in the prevention of tetanus, diphtheria, and pertussis infections.1 Protective antibodies in the pregnant woman, induced by routine immunization or natural antigenic exposure, are transferred across the placenta to the fetus and transiently protect the newborn from a variety of childhood infections. Transfer is initiated by the binding of immunoglobulins to Fc receptors on the membrane of trophoblasts in the placenta, followed by receptor-mediated endocytosis and active transport. IgG is the only immunoglobulin isotype transported, and IgG1 . . .