Normal pregnancies depend on successful implantation of the placenta i
n the uterus. The trophoblast which forms the ultimate interface betwe
en the fetal and maternal tissue seems to lack the foreign (allo) anti
gens (namely HLA/TLX) required to induce immunological rejection react
ions in the mother. It was previously believed that the trophoblast ex
pressed paternal allo antigens and that successful pregnancies were de
pendent on so called 'kind' (non-cytotoxic or non-complement binding)
blocking antibodies in order to protect the fetal unit from maternal c
ytotoxic T-cells and -antibodies. Blocking antibodies attached to pate
rnal antigens on the trophoblast were assumed to prevent maternal cyto
toxic T cell and cytotoxic antibodies from recognising the trophoblast
as foreign tissue. On this assumption it was reasoned that transfusio
ns of paternal HLA-expressing lymphocytes would increase maternal anti
paternal HLA (TLX) blocking antibodies and thus be beneficial to women
who experienced multiple miscarriages. There is, however, no scientif
ic evidence for a specific immune response after lymphocyte transfusio
ns that fulfil this function. Immunological tests, as for example mixe
d lymphocyte culture (MLC), on peripheral blood lymphocytes do not see
m to reflect the local immune state in the uterus, either in the pregn
ant or the non-pregnant state. Since the trophoblast forms the ultimat
e interface between fetal and maternal tissue, its structure, secretio
ns, and interaction with the decidua must be of definite importance fo
r implantation of the blastocyst and growth of the embryo.