A. Gasparoni et al., Immunophenotypic changes of fetal cord blood hematopoietic progenitor cells during gestation, PEDIAT RES, 47(6), 2000, pp. 825-829
We measured cell surface expression of CD34, HLA-DR, CD38, CD19, CD33, CD71
, and CD45 antigens in the hematopoietic progenitor cells of fetal cord blo
od to investigate immunophenotypic changes at different gestational ages. T
hese antigens were identified by flow cytometry in 11 fetuses (gestational
age 19-24 wk, in 12 preterm (25-28 wk) and in ten newborn infants born at t
erm. The frequency and number of CD34(+) cells were higher in the blood of
the 11 fetuses; in addition, a statistically significant inverse correlatio
n between number of CD34(+) cells and advancing gestational age was noted.
The numbers of CD34(+)CD19(+), CD34(+)CD33(+), and CD34(+)CD45(+) coexpress
ing cells were significantly higher in the fetuses, whereas CD34(+)CD38(+)
cells were more represented in the neonates at term. Gestational age was in
versely correlated with the number of CD34(+)CD19(+) and CD34(+)CD33(+) coe
xpressing cells. A positive correlation between gestational age and CD34(+)
D38(+) cells was noted. The number of CD34(-)CD19(+), CD34(-)CD38(+), and C
D34(-)CD45(+) cells was higher in term infants; furthermore, a significant
correlation between advancing gestational age and CD34(-)CD38(+) or CD34(-)
CD45(+) cells was demonstrated. The proliferative capacity was also higher
at lower gestational ages. These data suggest that the development and line
age commitment of fetal cord blood hematopoietic progenitor cells are very
active during the last two trimesters of pregnancy. The most significant ch
anges of hematopoietic cells maturation seem to occur within 25 wk of gesta
tion.