L. Bobroski et al., Mechanisms of transplacental transmission of HIV-1: I. Infection of fetal placental layers in the intervillous spaces, APPL IMMUNO, 7(4), 1999, pp. 271-279
Mother-to-child transmission of human immunodeficiency virus type 1 (HIV-1)
occurs in 6-50% of children born to HIV-1-seropositive mothers. It remains
unclear why some mothers transmit HIV-I to their infants, whereas the majo
rity do not. Studies to date indicate that multiple factors are associated
with maternal-fetal transmission including plasma viremia, maternal immune
response, maternal viral phenotypes, use of antiretroviral agents during pr
egnancy, and obstetrical factors. Little is known about the mode of transmi
ssion or the risk factors associated with transmission in utero. To determi
ne the location of fetal cell layers infected with HIV-1 and origin of vira
lly infected cells, a multiplex in situ polymerase chain reaction (PCR) tec
hnique was developed. For this purpose, maternal and fetal peripheral blood
mononuclear cells (PMBCs) were first typed for human leukocyte antigen (HL
A)-DQa by solution-based PCR method, and then various layers of placenta we
re examined for the presence of HIV-1-infected cells, DNA-IS-PCR, and the o
rigin of HIV-1 infected cells by reverse-transcriptase-initiated (RT) IS-PC
R for the expression of messenger RNA (mRNA) present in the maternal cells
but not inherited by the newborn, simultaneously. We analyzed 68 placentas
from HIV-1-infected mothers for the presence of HIV-1 proviral sequences, b
y using DNA-IS-PCR, expression of HIV-1 RNA (by RT-IS-PCR), and presence of
maternal cells by multiplex in situ PCR for the maternal-specific HLA-DQa
genes, not inherited by the baby, and IS-PCR for HIV-1. Our data revealed t
hat HIV-1-positive provirus sequences were present in the maternal cells in
15 (22%) of 68 placentas. In this group, numerous endothelial cells lining
the intervillous spaces of maternal decidua also were found to be infected
with HIV-1, In addition, 13 (19.6%) of 15 placentas (which were positive f
or HIV-1 provirus by DNA-IS-PCR) showed HIV-1-infected cells within the cho
rioamniotic layers. Our data strongly suggest that several fetal layers of
placenta become infected with HIV-1 through penetration of HIV-1-infected m
aternal cells. These studies are still in progress. Histologic observations
combined with IS-PCR and immunohistochemistry findings also are described.