It is well known that the transfer of immunoglobulins (Igs) from mother to
young via milk contributes to the offspring's immune defense. The present s
tudy suggests that not only is IgG transmitted to progeny, but that functio
nal maternal Ig-secreting cells (or B cells) can also be transferred to the
neonate. We have used B cell-deficient (mu (-/-)) mice and found that a hi
gh proportion of them obtain long-lasting, partial reconstitution of their
serum Ig levels if born to mu (+/-) mothers. In some of these serum IgG-pos
itive mu (-/-) mice, Ig-secreting cells were detected in spleen and bone ma
rrow To ensure that cells of maternal origin were present in the progeny, m
u (-/-) offspring born to mu (-/-) dams transgenic for green fluorescent pr
otein (GFP) were used. In spleens and bone marrow from some of these mu (-/
-)GFP(-/-) offspring, GFP-positive cells were detected, which demonstrated
that cells of maternal origin could infiltrate the progeny. In addition, sp
lenic Ig-secreting cells were detected in mu (-/-) mice that were born to m
u (-/-) dams and transferred to a lactating mu (+/+) foster dam at birth. T
his indicates that maternal Ig-secreting cells can be transferred postnatal
ly via milk.