PROBLEM: Pregnancy can be considered as a model of successfully controlled
tissue invasion. Cellular mediated immunity appears to regulate the control
led invasion of fetal trophoblast cells. In endometrium cancer, a dysregula
tion of invasive malignant cells can be observed. Since immuncompetent cell
s are known to be involved in recognition and rejection of 'non-self' antig
ens, we investigated the presence and distribution pattern of CD3, CD8, CD5
6, and CD68 positive cells in decidua from normal and failing pregancies, c
ompared with malignant and benign endometrium.
METHOD OF STUDY: Decidual tissue from first trimester normal pregancies (NP
; n = 15) and abortion (AB; n = 12), endometrial samples from premenopausal
women (NE; n = 8), and endometrioid adenocarcinoma (EA; n = 8) were examin
ed by immunohistochemistry using monoclonal antibody against large spectrum
cytokeratin, and against the receptors CD3, CD8, CD56 and CD68, respective
ly.
RESULTS: In NP, we observed 32.5% CD3, 44.7% CD56, and 22.9% CD68 (+) cells
. In AB, we found 36.9% CD3, 45.3% CD56, and 17.8% CD68 (+) cells. The diff
erences in ratio between normal pregnancy and abortion were not statistical
ly significant. In NE, we counted 39.5% CD3, 30.2% CD56 and 30.2% CD68 (+)
cells. In EA, we observed 47.9% CD3, 12.4% CD56 and 39.7% CD68 (+) cells. T
he decrease of CD56 positive cells in endometrioid adenocarcinoma was stati
stically significant. Interestingly, we found 4.1% of cells positive for CD
8 in NP, 4.9% in AB, 22.7% in NE, and 48.2% in EA. CONCLUSIONS: The increas
e of CD8 cells in NE, and particularely in EA, and decrease of CD56 cells,
compared with NP or BE, suggests an interaction between CD8 cells and CD56
cells. Studying different pathological situations in the uterus, such as ma
lignancies or ectopic pregnancies, might help us to understand the mechanis
ms involved in the maintenance of pregnancy.