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1.
Placenta ; 28(1): 1-5, 2007 Jan.
Article in English | MEDLINE | ID: mdl-16620961

ABSTRACT

Trafficking of cells between the fetus and its mother provides indirect clues to the underlying pathophysiology of pregnancy. Georg Schmorl first documented the presence of fetal cells in the maternal body and emphasized the importance of the placenta in eclampsia. Although his classic paper, written in 1893, is widely cited today, few investigators have actually read the paper, as it was published in German [Schmorl G., Pathologisch-anatomische Untersuchungen über Puerperal-Eklampsie. Verlag FCW Vogel, Leipzig; 1893]. Our goal was to translate the paper into English and critically re-evaluate its conclusions from a 21st century perspective. Schmorl was remarkably astute in his assessment of the pathologic changes that were seen in the 17 women on whom he performed complete autopsies. He found similar severe changes in all of the women, implying a common pathogenesis. This was in direct contrast to the then current doctrine. He was the first to observe the presence of thrombi containing multinucleated syncytial giant cells in the lungs of the women and speculated that they were of placental origin. To support his hypothesis he performed animal experiments. He also recognized that feto-maternal trafficking occurred in normal gestations but was increased in pregnancies affected by eclampsia. Using sophisticated molecular techniques we can now precisely confirm what Schmorl so elegantly described.


Subject(s)
Maternal-Fetal Exchange , Pre-Eclampsia/blood , Trophoblasts/physiology , Female , History, 19th Century , Humans , Obstetrics/history , Pregnancy
2.
Placenta ; 22(4): 309-16, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11286566

ABSTRACT

Pre-eclampsia is a disorder of unknown aetiology peculiar to human pregnancy. A well-described pathological feature being shallow trophoblast invasion into the spiral arteries during placenta development. Epidemiological studies have revealed an increased risk in pregnancies of primipaternity, and an association with the maternal-fetal HLA-DR relationship, both suggesting the involvement of an immunological component. We were therefore interested in the distribution of HLA-DR expressing myeloid cells in the decidua of healthy and pre-eclamptic placentae. We have studied the monocytes in maternal and fetal peripheral blood as well as in the placenta and identified the cluster of differentiation (CD) 14(+)myeloid cells in the basal plate as mannose receptor (ManR) positive tissue macrophages. In a comparison between peripheral blood monocytes from healthy pregnant and pre-eclamptic women we found no significant difference in the subpopulation size of CD14(+)/CD16(+)monocytes. The number and location of macrophages in the placental villi was similar. However, while the basal plate of the normal decidua contained numerous CD14(+), HLA-DR(bright), ManR(+)tissue macrophages, this compartment was virtually void of these phagocytic cells in the pre-eclamptic placenta. This novel finding suggests that in pre-eclampsia not only the migration of endovascular cytotrophoblasts is disturbed, but that also maternal macrophage migration is affected.


Subject(s)
Lectins, C-Type , Macrophages/pathology , Mannose-Binding Lectins , Pre-Eclampsia/pathology , Adult , Cell Count , Female , Flow Cytometry , HLA-DR Antigens/analysis , Humans , Immunohistochemistry , Immunophenotyping , Lipopolysaccharide Receptors/analysis , Macrophages/immunology , Mannose Receptor , Placenta/pathology , Platelet Endothelial Cell Adhesion Molecule-1/analysis , Pregnancy , Receptors, Cell Surface/analysis , Receptors, IgG/analysis
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