Fetal cells and cell-free fetal DNA in maternal blood: new insights into pre-eclampsia

被引:60
作者
Hahn, S [1 ]
Holzgreve, W [1 ]
机构
[1] Univ Basel, Univ Womens Hosp, CH-4031 Basel, Switzerland
关键词
cell-free DNA; fetal cells; hypothesis; maternal blood; pre-eclampsia;
D O I
10.1093/humupd/8.6.501
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The examination of fetal cells, specifically erythroblasts, and cell-free fetal DNA from the blood of pregnant women is currently the subject of intense research with the aim of developing new risk-free methods for prenatal diagnosis. An unexpected finding made during these studies was that the traffic of fetal erythroblasts into the maternal peripheral circulation was enhanced in pre-eclampsia. Independent prospective studies examining samples collected in the second trimester indicated that this perturbation in fetal cell trafficking occurs early in pregnancy, well before the onset of pre-eclampsia symptoms. The quantitative analysis of cell-free fetal and maternal DNA levels indicated that these concentrations were elevated in a co-ordinate manner in manifest pre-eclampsia, and that these elevations corresponded to disease severity. On the other hand, analysis of prospectively collected samples indicated that only cell-free fetal but not maternal DNA levels were elevated before onset of symptoms in pregnancies which subsequently developed pre-eclampsia. These data support hypotheses suggesting that pre-eclampsia is a multi-step disorder, initiated by a placental lesion that occurs early in pregnancy and which subsequently leads to a systemic maternal inflammatory response and associated endothelial cell damage.
引用
收藏
页码:501 / 508
页数:8
相关论文
共 85 条
[1]   Increased fetal erythroblasts in women who subsequently develop pre-eclampsia [J].
Al-Mufti, R ;
Hambley, H ;
Albaiges, G ;
Lees, C ;
Nicolaides, KH .
HUMAN REPRODUCTION, 2000, 15 (07) :1624-1628
[2]   Fetal cells in maternal blood of pregnancies with severe fetal growth restriction [J].
Al-Mufti, R ;
Lees, C ;
Albaiges, G ;
Hambley, H ;
Nicolaides, KH .
HUMAN REPRODUCTION, 2000, 15 (01) :218-221
[3]   Fetal DNA in skin of polymorphic eruptions of pregnancy [J].
Aractingi, S ;
Berkane, N ;
Bertheau, P ;
Le Goué, C ;
Dausset, J ;
Uzan, S ;
Carosella, ED .
LANCET, 1998, 352 (9144) :1898-1901
[4]   Persistent maternally derived peripheral microchimerism is associated with the juvenile idiopathic inflammatory myopathies [J].
Artlett, CM ;
Miller, FW ;
Rider, LG .
RHEUMATOLOGY, 2001, 40 (11) :1279-1284
[5]   Chimeric cells of maternal origin in juvenile idiopathic inflammatory myopathies [J].
Artlett, CM ;
Ramos, R ;
Jiminez, SA ;
Patterson, K ;
Miller, FW ;
Rider, LG .
LANCET, 2000, 356 (9248) :2155-2156
[6]  
ATTWOOD HD, 1961, J OBSTET GYN BR COMM, V68, P611
[7]   A new model for the origins of chronic disease. [J].
Barker D.J. .
Medicine, Health Care and Philosophy, 2001, 4 (1) :31-35
[8]  
Bianchi DW, 2001, ANN NY ACAD SCI, V945, P119
[9]   Fetal cells in the mother: from genetic diagnosis to diseases associated with fetal cell microchimerism [J].
Bianchi, DW .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2000, 92 (01) :103-108
[10]  
Brosens I A, 1972, Obstet Gynecol Annu, V1, P177