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against certain infections in neonates, such as GBS infection. A lack of type-specific maternal antibodies is associated with an increased risk of GBS sepsis.
Furthermore, active transplacental transport of
Pre-Term Immunity
Serum IgG levels in preterm infants born prior to 32
weeks are usually 2-4 times lower than those of term infants.
The defence mechanism in neonates are more
and phagocytic activities appear to be less effective , particularly during stress (eg. Sepsis, surgery)
Pre-Term Immunity
Cell-mediated immunity in preterm and newborn
tissues than term infants, and consequently, their mobilization of natural defences may be poorer.
Inflammatory responses in immature hosts are also
deficient.
Pre-Term Immunity
Young and adult rabbits have been shown to have
different capacities to develop and localize inflammation at the site of injection of pneumococci.
In adult rabbits, a very extensive localinflammation
Pre-Term Immunity
In contrast, young rabbits fail to develop extensive
(51% had no reaction, 36% had local redness only and 13% had redness and swelling).
Human newborns react similarly.
Textbook of Neonatal Medicine: A Chinese Perspective Hong Kong University Press, 1996 - 912 pages