The Fas-Fas ligand (FasL) pathway of apoptosis is abnormally activated in d
iseases associated with impaired immune tolerance or chronic inflammation.
Pregnancy-related hypertension is a spectrum of disease that commonly cause
s significant morbidity in women and in their newborn infants, is associate
d with generalized inflammation, and may be causally related to impaired ma
ternal-fetal tolerance. Our recent observation of enhanced trophoblast expr
ession of FasL in one form of pregnancy-related hypertension led us to hypo
thesize that this group of disorders might be associated with abnormal acti
vation of the Fas-FasL pathway. To test this hypothesis, we prospectively q
uantified soluble and leukocyte-associated Fas receptor and FasL in the mat
ernal and umbilical cord blood (CB) sera of 20 gestations complicated by pr
eeclampsia and of 18 normal control gestations, using ELISA and flow cytome
tric analyses. We determined higher soluble FasL levels in paired maternal
and CB sera of hypertensive gestations compared with control gestations (p
< 0.01) in contrast, soluble Fas levels were similar between groups. Surfac
e expression of FasL was lower on maternal (p < 0.01) and CB (p < 0.05) neu
trophils from affected gestations, whereas surface Fas expression was lower
on maternal (p < 0.02), but not CB, neutrophils and lymphocytes. We conclu
de that expression of Fas and FasL in sera and on leukocytes is altered in
gestations complicated by preeclampsia, and speculate that activation of th
e Fas-FasL pathway mediates associated pathologic processes in affected wom
en and in their neonates.